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  • 1.
    Abrahamsson, Annelie
    et al.
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten.
    Rasti Boroojeni, Fatemeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Naeimipour, Sajjad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Reustle, Nina
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Dabrosin, Charlotta
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Centrum för kirurgi, ortopedi och cancervård, Onkologiska kliniken US.
    Increased matrix stiffness enhances pro-tumorigenic traits in a physiologically relevant breast tissue- monocyte 3D model2024Ingår i: Acta Biomaterialia, ISSN 1742-7061, E-ISSN 1878-7568, Vol. 178, s. 160-169Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    High mammographic density, associated with increased tissue stiffness, is a strong risk factor for breast cancer per se . In postmenopausal women there is no differences in the occurrence of ductal carcinoma in situ (DCIS) depending on breast density. Preliminary data suggest that dense breast tissue is associated with a pro -inflammatory microenvironment including infiltrating monocytes. However, the underlying mechanism(s) remains largely unknown. A major roadblock to understanding this risk factor is the lack of relevant in vitro models. A biologically relevant 3D model with tunable stiffness was developed by cross -linking hyaluronic acid. Breast cancer cells were cultured with and without freshly isolated human monocytes. In a unique clinical setting, extracellular proteins were sampled using microdialysis in situ from women with various breast densities. We show that tissue stiffness resembling high mammographic density increases the attachment of monocytes to the cancer cells, increase the expression of adhesion molecules and epithelia-mesenchymal-transition proteins in estrogen receptor (ER) positive breast cancer. Increased tissue stiffness results in increased secretion of similar pro-tumorigenic proteins as those found in human dense breast tissue including inflammatory cytokines, proteases, and growth factors. ER negative breast cancer cells were mostly unaffected suggesting that diverse cancer cell phenotypes may respond differently to tissue stiffness. We introduce a biological relevant model with tunable stiffness that resembles the densities found in normal breast tissue in women. The model will be key for further mechanistic studies. Additionally, our data revealed several pro-tumorigenic pathways that may be exploited for prevention and therapy against breast cancer.

  • 2.
    Ahmed, Fareed
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ding, Penghui
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ail, Ujwala
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Warczak, Magdalena
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Grimoldi, Andrea
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Håkansson, Karl M. O.
    RISE Bioeconomy, Stockholm, Sweden.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Gueskine, Viktor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Manufacturing Poly(3,4-Ethylenedioxythiophene) Electrocatalytic Sheets for Large-Scale H2O2 Production2022Ingår i: Advanced Sustainable Systems, E-ISSN 2366-7486, Vol. 6, nr 1, artikel-id 2100316Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Producing thick films of conducting polymers by a low-cost manufacturing technique would enable new applications. However, removing huge solvent volume from diluted suspension or dispersion (1-3 wt%) in which conducting polymers are typically obtained is a true manufacturing challenge. In this work, a procedure is proposed to quickly remove water from the conducting polymer poly(3,4-ethylenedioxythiophene:poly(4-styrene sulfonate) (PEDOT:PSS) suspension. The PEDOT:PSS suspension is first flocculated with 1 m H2SO4 transforming PEDOT nanoparticles (approximate to 50-500 nm) into soft microparticles. A filtration process inspired by pulp dewatering in a paper machine on a wire mesh with apertures dimension between 60 mu m and 0.5 mm leads to thick free-standing films (approximate to 0.5 mm). Wire mesh clogging that hinders dewatering (known as dead-end filtration) is overcome by adding to the flocculated PEDOT: PSS dispersion carbon fibers that aggregate and form efficient water channels. Moreover, this enables fast formation of thick layers under simple atmospheric pressure filtration, thus making the process truly scalable. Thick freestanding PEDOT films thus obtained are used as electrocatalysts for efficient reduction of oxygen to hydrogen peroxide, a promising green chemical and fuel. The inhomogeneity of the films does not affect their electrochemical function.

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  • 3.
    Ali, Hala R.
    et al.
    Agr Res Ctr ARC, Egypt.
    Selim, Salah A.
    Cairo Univ, Egypt.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Effects of macrophage polarization on gold nanoparticle-assisted plasmonic photothermal therapy2021Ingår i: RSC Advances, E-ISSN 2046-2069, Vol. 11, nr 40, s. 25047-25056Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Tumor associated macrophages (TAM) are key pathogenic factors in neoplastic diseases. They are known to have plasticity and can polarize into two opposing phenotypes, including the tumoricidal M1 and the protumoral M2 phenotypes with high prevalence of M2-phentoypes in patients with poor prognosis. Strategies for targeting M2-TAM may consequently increase the efficacy of therapeutic strategies for cancer treatment. Gold nanorod-assisted plasmonic photothermal therapy (PPTT) has emerged as a promising treatment for cancer but the effects of macrophage polarization parameters in the performance of this new treatment modality is still unknown. Herein, human monocytic THP-1 cells were polarized into two opposite phenotypic macrophages (M1-TAM and M2-TAM) and their response to PPTT was examined. M2-TAM exhibits a three-fold increase in AuNP uptake compared to M1-TAM. Laser irradiation results in selective killing of pro-tumoral M2-TAM after treatment with AuNPs with limited effects on anti-tumoral M1-TAM. A positive correlation between the expression of CD206 marker and the AuNP uptake may indicate the role of CD206 in facilitating AuNP uptake. Our findings also suggest that the differences in AuNP avidity and uptake between the M1-TAM and M2-TAM phenotypes may be the rationale behind the effectiveness of PPTT in the treatment of solid tumors.

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  • 4.
    Arja, Katriann
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Paloncyova, Marketa
    KTH Royal Inst Technol, Sweden; Palacky Univ Olomouc, Czech Republic.
    Linares, Mathieu
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Lindgren, Mikael
    Norwegian Univ Sci & Technol, Norway.
    Norman, Patrick
    KTH Royal Inst Technol, Sweden.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Nilsson, Peter
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Self-Assembly of Chiro-Optical Materials from Nonchiral Oligothiophene-Porphyrin Derivatives and Random Coil Synthetic Peptides2023Ingår i: ChemPlusChem, E-ISSN 2192-6506, Vol. 88, nr 1Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Biomimetic chiral optoelectronic materials can be utilized in electronic devices, biosensors and artificial enzymes. Herein, this work reports the chiro-optical properties and architectural arrangement of optoelectronic materials generated from self-assembly of initially nonchiral oligothiophene-porphyrin derivatives and random coil synthetic peptides. The photo-physical- and structural properties of the materials were assessed by absorption-, fluorescence- and circular dichroism spectroscopy, as well as dynamic light scattering, scanning electron microscopy and theoretical calculations. The materials display a three-dimensional ordered helical structure and optical activity that are observed due to an induced chirality of the optoelectronic element upon interaction with the peptide. Both these properties are influenced by the chemical composition of the oligothiophene-porphyrin derivative, as well as the peptide sequence. We foresee that our findings will aid in developing self-assembled optoelectronic materials with dynamic architectonical accuracies, as well as offer the possibility to generate the next generation of materials for a variety of bioelectronic applications.

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  • 5.
    Aronsson, Christopher
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Jury, Michael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Naeimipour, Sajjad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rasti Boroojeni, Fatemeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Christoffersson, Jonas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teknisk biologi. Linköpings universitet, Tekniska fakulteten. Univ Skovde, Sweden.
    Lifwergren, Philip
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Mandenius, Carl-Fredrik
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Dynamic peptide-folding mediated biofunctionalization and modulation of hydrogels for 4D bioprinting2020Ingår i: Biofabrication, ISSN 1758-5082, E-ISSN 1758-5090, Vol. 12, nr 3, artikel-id 035031Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Hydrogels are used in a wide range of biomedical applications, including three-dimensional (3D) cell culture, cell therapy and bioprinting. To enable processing using advanced additive fabrication techniques and to mimic the dynamic nature of the extracellular matrix (ECM), the properties of the hydrogels must be possible to tailor and change over time with high precision. The design of hydrogels that are both structurally and functionally dynamic, while providing necessary mechanical support is challenging using conventional synthesis techniques. Here, we show a modular and 3D printable hydrogel system that combines a robust but tunable covalent bioorthogonal cross-linking strategy with specific peptide-folding mediated interactions for dynamic modulation of cross-linking and functionalization. The hyaluronan-based hydrogels were covalently cross-linked by strain-promoted alkyne-azide cycloaddition using multi-arm poly(ethylene glycol). In addition, ade novodesigned helix-loop-helix peptide was conjugated to the hyaluronan backbone to enable specific peptide-folding modulation of cross-linking density and kinetics, and hydrogel functionality. An array of complementary peptides with different functionalities was developed and used as a toolbox for supramolecular tuning of cell-hydrogel interactions and for controlling enzyme-mediated biomineralization processes. The modular peptide system enabled dynamic modifications of the properties of 3D printed structures, demonstrating a novel route for design of more sophisticated bioinks for four-dimensional bioprinting.

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  • 6.
    Baş, Yağmur
    et al.
    Division of Materials Science, Luleå University of Technology, Sweden.
    Berglund, Linn
    Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden..
    Niittylä, Totte
    Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden..
    Zattarin, Elisa
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik.
    Aili, Daniel
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik.
    Sotra, Zeljana
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Rinklake, Ivana
    Linköpings universitet, Medicinska fakulteten. Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Junker, Johan
    Linköpings universitet, Medicinska fakulteten. Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Rakar, Jonathan
    Linköpings universitet, Medicinska fakulteten. Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Oksman, Kristiina
    Division of Materials Science, Luleå University of Technology, Sweden ; Department of Mechanical & Industrial Engineering (MIE), University of Toronto, Ontario, Canada.
    Preparation and Characterization of Softwood and Hardwood Nanofibril Hydrogels: Toward Wound Dressing Applications.2023Ingår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 24, nr 12, s. 5605-5619Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Hydrogels of cellulose nanofibrils (CNFs) are promising wound dressing candidates due to their biocompatibility, high water absorption, and transparency. Herein, two different commercially available wood species, softwood and hardwood, were subjected to TEMPO-mediated oxidation to proceed with delignification and oxidation in a one-pot process, and thereafter, nanofibrils were isolated using a high-pressure microfluidizer. Furthermore, transparent nanofibril hydrogel networks were prepared by vacuum filtration. Nanofibril properties and network performance correlated with oxidation were investigated and compared with commercially available TEMPO-oxidized pulp nanofibrils and their networks. Softwood nanofibril hydrogel networks exhibited the best mechanical properties, and in vitro toxicological risk assessment showed no detrimental effect for any of the studied hydrogels on human fibroblast or keratinocyte cells. This study demonstrates a straightforward processing route for direct oxidation of different wood species to obtain nanofibril hydrogels for potential use as wound dressings, with softwood having the most potential.

  • 7.
    Bengtsson, Torbjorn
    et al.
    Orebro Univ, Sweden.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Orebro Univ, Sweden.
    Musa, Amani
    Orebro Univ, Sweden.
    Hultenby, Kjell
    Karolinska Inst, Sweden.
    Utterström, Johanna
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Sivler, Petter
    S2Medical AB, SE-58273 Linkoping, Sweden.
    Skog, Marten
    S2Medical AB, SE-58273 Linkoping, Sweden.
    Nayeri, Fariba
    PEAS Res Inst, Dept Infect Control, SE-58273 Linkoping, Sweden.
    Hellmark, Bengt
    Orebro Univ Hosp, Sweden.
    Soderquist, Bo
    Orebro Univ, Sweden; Orebro Univ Hosp, Sweden.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Khalaf, Hazem
    Orebro Univ, Sweden.
    Plantaricin NC8 alpha beta exerts potent antimicrobial activity against Staphylococcus spp. and enhances the effects of antibiotics2020Ingår i: Scientific Reports, E-ISSN 2045-2322, Vol. 10, nr 1, artikel-id 3580Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The use of conventional antibiotics has substantial clinical efficacy, however these vital antimicrobial agents are becoming less effective due to the dramatic increase in antibiotic-resistant bacteria. Novel approaches to combat bacterial infections are urgently needed and bacteriocins represent a promising alternative. In this study, the activities of the two-peptide bacteriocin PLNC8 alpha beta were investigated against different Staphylococcus spp. The peptide sequences of PLNC8 alpha and beta were modified, either through truncation or replacement of all L-amino acids with D-amino acids. Both L- and D-PLNC8 alpha beta caused rapid disruption of lipid membrane integrity and were effective against both susceptible and antibiotic resistant strains. The D-enantiomer was stable against proteolytic degradation by trypsin compared to the L-enantiomer. Of the truncated peptides, beta 1-22, beta 7-34 and beta 1-20 retained an inhibitory activity. The peptides diffused rapidly (2min) through the bacterial cell wall and permeabilized the cell membrane, causing swelling with a disorganized peptidoglycan layer. Interestingly, sub-MIC concentrations of PLNC8 alpha beta substantially enhanced the effects of different antibiotics in an additive or synergistic manner. This study shows that PLNC8 alpha beta is active against Staphylococcus spp. and may be developed as adjuvant in combination therapy to potentiate the effects of antibiotics and reduce their overall use.

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  • 8.
    Bengtsson, Torbjörn
    et al.
    Örebro University, Sweden.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Örebro University, Sweden.
    Musa, Amani
    Örebro University, Sweden.
    Hultenby, Kjell
    Karolinska Institutet, Sweden.
    Utterström, Johanna
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Sivlér, Petter
    S2Medical AB, 58273, Linköping, Sweden.
    Skog, Mårten
    S2Medical AB, 58273, Linköping, Sweden.
    Nayeri, Fariba
    Department of Infection Control, PEAS Research Institute, Linköping, Sweden.
    Hellmark, Bengt
    Department of Clinical Microbiology, Örebro University Hospital, Sweden.
    Söderquist, Bo
    Cardiovascular Research Centre, School of Medical Sciences, Örebro University, 70362, Örebro, Sweden; Department of Clinical Microbiology, Örebro University Hospital, Sweden.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Khalaf, Hazem
    Cardiovascular Research Centre, School of Medical Sciences, Örebro University, Sweden.
    Author Correction: Plantaricin NC8 aß exerts potent antimicrobial activity against Staphylococcus spp. and enhances the effects of antibiotics2020Ingår i: Scientific Reports, E-ISSN 2045-2322, Vol. 10, nr 1Artikel i tidskrift (Övrigt vetenskapligt)
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  • 9.
    Berglund, Linn
    et al.
    Luleå University of Technology, Sweden.
    Squinca, Paula
    Luleå University of Technology, Sweden; Embrapa Instrumentation, Brazil.
    Baş, Yağmur
    Luleå University of Technology, Sweden.
    Zattarin, Elisa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik.
    Rakar, Jonathan
    Linköpings universitet, Medicinska fakulteten. Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Junker, Johan
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Starkenberg, Annika
    Linköpings universitet, Medicinska fakulteten. Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Diamanti, Mattia
    Luleå University of Technology, Sweden.
    Sivlér, Petter
    S2Medical AB, Sweden.
    Skog, Mårten
    S2Medical AB, Sweden.
    Oksman, Kristiina
    Luleå University of Technology, Sweden.
    Self-Assembly of Nanocellulose Hydrogels Mimicking Bacterial Cellulose for Wound Dressing Applications2023Ingår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 24, nr 5, s. 2264-2277Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The self-assembly of nanocellulose in the form of cellulose nanofibers (CNFs) can be accomplished via hydrogen-bonding assistance into completely bio-based hydrogels. This study aimed to use the intrinsic properties of CNFs, such as their ability to form strong networks and high absorption capacity and exploit them in the sustainable development of effective wound dressing materials. First, TEMPO-oxidized CNFs were separated directly from wood (W-CNFs) and compared with CNFs separated from wood pulp (P-CNFs). Second, two approaches were evaluated for hydrogel self-assembly from W-CNFs, where water was removed from the suspensions via evaporation through suspension casting (SC) or vacuum-assisted filtration (VF). Third, the W-CNF-VF hydrogel was compared to commercial bacterial cellulose (BC). The study demonstrates that the self-assembly via VF of nanocellulose hydrogels from wood was the most promising material as wound dressing and displayed comparable properties to that of BC and strength to that of soft tissue.

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  • 10.
    Björk, Linnea
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Bäck, Marcus
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Hammarström, Per
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Lindgren, Mikael
    Norwegian Univ Sci & Technol, Norway.
    Nilsson, Peter
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Amino-Acid Side-Chain Nanoarchitectonics for Tuning the Chiroptical Properties and Supramolecular Structure of Pentameric Oligothiophenes2024Ingår i: ChemPhotoChem, E-ISSN 2367-0932Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Oligothiophenes with specific photophysical properties and molecular organization are of great interest, since this class of materials are used in organic electronics and bioelectronics, as well as biosensing. Herein, 8 different pentameric oligothiophenes, denoted proteophenes, with different amino acid substitution patterns at distinct positions along the thiophene backbone were investigated. Spectroscopic and microscopic studies of the ligands revealed the formation of optically active self-assembled materials under acidic or basic conditions. The distinct photophysical characteristics, including induced circular dichroism, as well as the supramolecular structures of the assemblies deduced from light scattering and transmission electron microscopy, were highly influenced by the positioning of distinct amino acid moieties along the thiophene backbone. Proteophenes functionalized with only glutamate residues or these functionalities in combination with hydrophobic valine moieties formed fibrillar structures with excellent chiroptical properties under acidic conditions. In addition, the amino acid functionality at the beta-position of distinct thiophene moieties influenced the induced circular dichroism pattern observed from the proteophenes. Overall, the obtained results demonstrate how changes in the position of various amino acid functionalities, as well as the chemical nature of the amino acid side chain functionality greatly affect the optical properties as well as the architecture of the self-assembled materials. Self-assembled Proteophenes. Oligothiophenes with distinct amino acid side-chain functionalities along the conjugated backbone displayed distinct chiroptical and structural properties in acidic or alkaline solutions. The distinct photophysical characteristics, as well as the supramolecular structures of the assemblies were highly influenced by the chemical nature of the amino acid, as well as the positioning of distinct amino acid moieties along the thiophene backbone.image

  • 11.
    Brechmann, Nils A.
    et al.
    KTH Royal Inst Technol, Sweden; KTH Royal Inst Technol, Sweden.
    Jansson, Marta
    AstraZeneca, Sweden.
    Hägg, Alice
    AstraZeneca, Sweden.
    Hicks, Ryan
    AstraZeneca, Sweden.
    Hyllner, Johan
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. AstraZeneca, Sweden.
    Eriksson, Kristofer
    MAG Bioproc, Sweden.
    Chotteau, Veronique
    KTH Royal Inst Technol, Sweden; KTH Royal Inst Technol, Sweden.
    Proof-of-Concept of a Novel Cell Separation Technology Using Magnetic Agarose-Based Beads2022Ingår i: Magnetochemistry, ISSN 2312-7481, Vol. 8, nr 3, artikel-id 34Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The safety of the cells used for Advanced Therapy Medicinal Products is crucial for patients. Reliable methods for the cell purification are very important for the commercialization of those new therapies. With the large production scale envisioned for commercialization, the cell isolation methods need to be efficient, robust, operationally simple and generic while ensuring cell biological functionality and safety. In this study, we used high magnetized magnetic agarose-based beads conjugated with protein A to develop a new method for cell separation. A high separation efficiency of 91% yield and consistent isolation performances were demonstrated using population mixtures of human mesenchymal stem cells and HER2(+) SKBR3 cells (80:20, 70:30 and 30:70). Additionally, high robustness against mechanical stress and minimal unspecific binding obtained with the protein A base conjugated magnetic beads were significant advantages in comparison with the same magnetic microparticles where the antibodies were covalently conjugated. This study provided insights on features of large high magnetized microparticles, which is promising for the large-scale application of cell purification.

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  • 12.
    Busch, Christian
    et al.
    Applied Physical Chemistry, Institute for Physical Chemistry, Heidelberg University, Heidelberg, Germany.
    Nagy, Bela
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Stöcklin, Andreas
    Applied Physical Chemistry, Institute for Physical Chemistry, Heidelberg University, Heidelberg, Germany.
    Gutfreund, Philipp
    Institut Laue-Langevin, France.
    Dahint, Reiner
    Applied Physical Chemistry, Institute for Physical Chemistry, Heidelberg University, Heidelberg, Germany.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    A mobile setup for simultaneous and in situ neutron reflectivity, infrared spectroscopy, and ellipsometry studies2022Ingår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 93, nr 11Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Neutron reflectivity at the solid/liquid interface offers unique opportunities for resolving the structure–function relationships of interfacial layers in soft matter science. It is a non-destructive technique for detailed analysis of layered structures on molecular length scales, providing thickness, density, roughness, and composition of individual layers or components of adsorbed films. However, there are also some well-known limitations of this method, such as the lack of chemical information, the difficulties in determining large layer thicknesses, and the limited time resolution. We have addressed these shortcomings by designing and implementing a portable sample environment for in situ characterization at neutron reflectometry beamlines, integrating infrared spectroscopy under attenuated total reflection for determination of molecular entities and their conformation, and spectroscopic ellipsometry for rapid and independent measurement of layer thicknesses and refractive indices. The utility of this combined setup is demonstrated by two projects investigating (a) pH-dependent swelling of polyelectrolyte layers and (b) the impact of nanoparticles on lipid membranes to identify potential mechanisms of nanotoxicity. 

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  • 13.
    Bäck, Marcus
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Todarwal, Yogesh
    KTH Royal Inst Technol, Sweden.
    Nyström, Sofie
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Norman, Patrick
    KTH Royal Inst Technol, Sweden.
    Linares, Mathieu
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Bioinformatik. Linköpings universitet, Tekniska fakulteten.
    Hammarström, Per
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Lindgren, Mikael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten. Norwegian Univ Sci & Technol, Norway.
    Nilsson, Peter
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten.
    Tyrosine Side-Chain Functionalities at Distinct Positions Determine the Chirooptical Properties and Supramolecular Structures of Pentameric Oligothiophenes2020Ingår i: ChemistryOpen, ISSN 2191-1363, Vol. 9, nr 11, s. 1100-1108Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Control over the photophysical properties and molecular organization of pi-conjugated oligothiophenes is essential to their use in organic electronics. Herein we synthesized and characterized a variety of anionic pentameric oligothiophenes with different substitution patterns of L- or D-tyrosine at distinct positions along the thiophene backbone. Spectroscopic, microscopic, and theoretical studies of L- or D-tyrosine substituted pentameric oligothiophene conjugates revealed the formation of optically active pi-stacked self-assembled aggregates under acid conditions. The distinct photophysical characteristics, as well as the supramolecular structures of the assemblies, were highly influenced by the positioning of the L- or D-tyrosine moieties along the thiophene backbone. Overall, the obtained results clearly demonstrate how fundamental changes in the position of the enantiomeric side-chain functionalities greatly affect the optical properties as well as the architecture of the self-assembled supramolecular structures.

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  • 14.
    Chen, Zhenzhong
    et al.
    School of Mechanical Engineering, Sungkyunkwan University (SKKU), Suwon, South Korea.
    Han, Seokgyu
    School of Mechanical Engineering, Sungkyunkwan University (SKKU), Suwon, South Korea.
    Sanny, Arleen
    Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), Singapore.
    Chan, Dorothy Leung-Kwan
    Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), Singapore.
    van Noort, Danny
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Centro de Investigación en Bioingeniería, Universidad de Ingenieria y Tecnologia - UTEC, Lima, Peru.
    Lim, Wanyoung
    Department of Biomedical Engineering, Sungkyunkwan University (SKKU), Suwon, South Korea.
    Tan, Andy Hee-Meng
    Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), Singapore.
    Park, Sungsu
    School of Mechanical Engineering, Sungkyunkwan University (SKKU), Suwon, South Korea; Department of Biomedical Engineering, Sungkyunkwan University (SKKU), Suwon, South Korea; Institute of Quantum Biophysics (IQB), Sungkyunkwan University (SKKU), Suwon, South Korea.
    3D hanging spheroid plate for high-throughput CART cell cytotoxicity assay2022Ingår i: Journal of Nanobiotechnology, E-ISSN 1477-3155, Vol. 20, nr 1, artikel-id 30Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Background: Most high-throughput screening (HIS) systems studying the cytotoxic effect of chimeric antigen receptor (CAR) T cells on tumor cells rely on two-dimensional cell culture that does not recapitulate the tumor micro-environment (TME). Tumor spheroids, however, can recapitulate the TME and have been used for cytotoxicity assays of CART cells. But a major obstacle to the use of tumor spheroids for cytotoxicity assays is the difficulty in separating unbound CART and dead tumor cells from spheroids. Here, we present a three-dimensional hanging spheroid plate (3DHSP), which facilitates the formation of spheroids and the separation of unbound and dead cells from spheroids during cytotoxicity assays.

    Results: The 3DHSP is a 24-well plate, with each well composed of a hanging dripper, spheroid wells, and waste wells. In the dripper, a tumor spheroid was formed and mixed with CART cells. In the 3DHSP, droplets containing the spheroids were deposited into the spheroid separation well, where unbound and dead T and tumor cells were separated from the spheroid through a gap into the waste well by tilting the 3DHSP by more than 20 degrees. Human epidermal growth factor receptor 2 (HER2)-positive tumor cells (BT474 and SKOV3) formed spheroids of approximately 300-350 pm in diameter after 2 days in the 3DHSP. The cytotoxic effects ofT cells engineered to express CAR recognizing HER2 (HER2-CAR T cells) on these spheroids were directly measured by optical imaging, without the use of live/dead fluorescent staining of the cells. Our results suggest that the 3DHSP could be incorporated into a HTS system to screen for CARs that enable T cells to kill spheroids formed from a specific tumor type with high efficacy or for spheroids consisting of tumor types that can be killed efficiently by T cells bearing a specific CAR.

    Conclusions: The results suggest that the 3DHSP could be incorporated into a HTS system for the cytotoxic effects of CART cells on tumor spheroids.

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  • 15. Beställ onlineKöp publikationen >>
    Eskilson, Olof
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Multifunctional Nanocellulose Composite Materials2023Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
    Abstract [en]

    Nanoparticles (NPs) are particles with more than one dimension between 1 and 100 nm. Because of their small size, they typically display different physical and chemical properties than the corresponding bulk materials. NPs have been used in many different applications, such as in electronics, optics, catalysis, and in biomedicine. Due to their colloidal nature, NPs are often immobilized on a solid substrate, such as glass or polymer-based materials, including biopolymers. Nanocellulose is a biopolymerbased nanomaterial that can be obtained from plants or bacterial biofilms. They can be processed into thin and highly hydrated films with high mechanical strength and can serve as a versatile substrate for NPs. Bacterial cellulose (BC) is also an interesting material for generating wound dressings. The combination of NPs and BC results in soft and flexible nanocomposites (BC-NPs) that can demonstrate novel properties and improve the functionality of wound dressings. 

    BC-NP nanocomposites have previously been obtained by impregnating BC with the reactants needed for synthesis of the NPs and allowing the reaction to proceed in situ, inside and on the surface of the BC. This strategy limits the possibilities to control NP geometry and NP concentration and make synthesis of nanocomposites with more sophisticated compositions very challenging. In addition, the synthesis conditions used can potentially have negative effects on the properties of BC. 

    The work presented in this thesis shows the possibility to produce well-defined, tunable BC-NP nanocomposites using self-assembly under very benign conditions that enable functionalization of BC with a wide range of different types of NPs. In addition to exploring the self-assembly process and the physical properties of these new BC-NP composites, several different applications were investigated. The functionalization of BC with gold nanoparticles (AuNPs) of different sizes and geometries was demonstrated. The resulting materials were used for development of a new sensor transduction technology, exploiting the optical response upon mechanical compression to detect biomolecules. BC-AuNP nanocomposites were also developed for monitoring of protease activity of wound pathogens, for catalysis, and for fabrication of ultra-black materials with unique absorption and scattering profiles of light in the visible and near infrared spectral range. In addition, the self-assembly process could be adopted for generating BC-mesoporous silica nanoparticles (MSNs) nanocomposite wound dressings. The resulting high surface area materials could be used as carriers for pH sensitive dyes. The pH-responsive BC-MSNs demonstrated adequate biocompatibility and allowed for monitoring of wound pH and for assessment of wound status. 

    The strategies for functionalization of BC with inorganic NPs that was developed and explored in this thesis are highly versatile and allow for fabrication of a wide range of multifunctional nanocomposite materials. 

    Delarbeten
    1. Self-Assembly of Mechanoplasmonic Bacterial Cellulose-Metal Nanoparticle Composites
    Öppna denna publikation i ny flik eller fönster >>Self-Assembly of Mechanoplasmonic Bacterial Cellulose-Metal Nanoparticle Composites
    Visa övriga...
    2020 (Engelska)Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 30, nr 40, artikel-id 2004766Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Nanocomposites of metal nanoparticles (NPs) and bacterial nanocellulose (BC) enable fabrication of soft and biocompatible materials for optical, catalytic, electronic, and biomedical applications. Current BC-NP nanocomposites are typically prepared by in situ synthesis of the NPs or electrostatic adsorption of surface functionalized NPs, which limits possibilities to control and tune NP size, shape, concentration, and surface chemistry and influences the properties and performance of the materials. Here a self-assembly strategy is described for fabrication of complex and well-defined BC-NP composites using colloidal gold and silver NPs of different sizes, shapes, and concentrations. The self-assembly process results in nanocomposites with distinct biophysical and optical properties. In addition to antibacterial materials and materials with excellent senor performance, materials with unique mechanoplasmonic properties are developed. The homogenous incorporation of plasmonic gold NPs in the BC enables extensive modulation of the optical properties by mechanical stimuli. Compression gives rise to near-field coupling between adsorbed NPs, resulting in tunable spectral variations and enhanced broadband absorption that amplify both nonlinear optical and thermoplasmonic effects and enables novel biosensing strategies.

    Ort, förlag, år, upplaga, sidor
    WILEY-V C H VERLAG GMBH, 2020
    Nyckelord
    antimicrobials; bacterial cellulose; gold nanoparticles; nanocomposite; sensors
    Nationell ämneskategori
    Materialkemi
    Identifikatorer
    urn:nbn:se:liu:diva-168770 (URN)10.1002/adfm.202004766 (DOI)000557380700001 ()
    Anmärkning

    Funding Agencies|Swedish Foundation for Strategic Research (SFF)Swedish Foundation for Strategic Research [FFL15-0026, RMX18-0039]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009-00971]; VinnovaVinnova [2016-05156]; Knut and Alice Wallenberg FoundationKnut & Alice Wallenberg Foundation [KAW 2016.0231]; Swedish Research CouncilSwedish Research Council [2017-05178, 2015-05002]; Spanish Ministerio de Ciencia, Innovacion y Universidades (MICINN) [MAT2016-77391-R]; Severo Ochoa Centres of Excellence programme - Spanish Research Agency (AEI) [SEV-2017-0706]

    Tillgänglig från: 2020-08-31 Skapad: 2020-08-31 Senast uppdaterad: 2023-05-24
    2. Nanocellulose composite wound dressings for real-time pH wound monitoring
    Öppna denna publikation i ny flik eller fönster >>Nanocellulose composite wound dressings for real-time pH wound monitoring
    Visa övriga...
    2023 (Engelska)Ingår i: Materials Today Bio, ISSN 2590-0064, Vol. 19, artikel-id 100574Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    The skin is the largest organ of the human body. Wounds disrupt the functions of the skin and can have catastrophic consequences for an individual resulting in significant morbidity and mortality. Wound infections are common and can substantially delay healing and can result in non-healing wounds and sepsis. Early diagnosis and treatment of infection reduce risk of complications and support wound healing. Methods for monitoring of wound pH can facilitate early detection of infection. Here we show a novel strategy for integrating pH sensing capabilities in state-of-the-art hydrogel-based wound dressings fabricated from bacterial nanocellulose (BC). A high surface area material was developed by self-assembly of mesoporous silica nanoparticles (MSNs) in BC. By encapsulating a pH-responsive dye in the MSNs, wound dressings for continuous pH sensing with spatiotemporal resolution were developed. The pH responsive BC-based nanocomposites demonstrated excellent wound dressing properties, with respect to conformability, mechanical properties, and water vapor transmission rate. In addition to facilitating rapid colorimetric assessment of wound pH, this strategy for generating functional BC-MSN nanocomposites can be further be adapted for encapsulation and release of bioactive compounds for treatment of hard-to-heal wounds, enabling development of novel wound care materials.

    Ort, förlag, år, upplaga, sidor
    Elsevier, 2023
    Nyckelord
    Bacterial nanocellulose, Wound dressing, pH sensor, Infection, Mesoporous silica nanoparticles
    Nationell ämneskategori
    Biomaterialvetenskap
    Identifikatorer
    urn:nbn:se:liu:diva-192408 (URN)10.1016/j.mtbio.2023.100574 (DOI)000944392500001 ()36852226 (PubMedID)
    Anmärkning

    Funding agencies: This work was supported by the Swedish Foundation for Strategic Research (SFF) grant no. FFL15-0026 and framework grant RMX18-0039 (HEALiX), the Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU no. 2009–00971), the competence center FunMat-II that is financially supported by Vinnova (grant no. 2016-05156), the Knut and Alice Wallenberg Foundation (grant no. KAW 2016.0231), the Swedish Research Council (VR) (grant no. 2021-04427) and Swedish strategic research program Bio4Energy. Illustrations were created with BioRender.com. We thank S2Medical AB, Linköping, Sweden, for providing BC.

    Tillgänglig från: 2023-03-15 Skapad: 2023-03-15 Senast uppdaterad: 2024-05-01Bibliografiskt granskad
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  • 16.
    Eskilson, Olof
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Lindström, Stefan B
    Linköpings universitet, Institutionen för ekonomisk och industriell utveckling, Mekanik och hållfasthetslära. Linköpings universitet, Tekniska fakulteten.
    Sepulveda, Borja
    CSIC, Spain; BIST, Spain.
    Shahjamali, Mohammad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Harvard Univ, MA 02138 USA.
    Guell-Grau, Pau
    CSIC, Spain.
    Sivlér, Petter
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Skog, Mårten
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Aronsson, Christopher
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Björk, Emma
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Nyberg, Niklas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Khalaf, Hazem
    Orebro Univ, Sweden.
    Bengtsson, Torbjorn
    Orebro Univ, Sweden.
    James, Jeemol
    Univ Gothenburg, Sweden.
    Ericson, Marica B.
    Univ Gothenburg, Sweden.
    Martinsson, Erik
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Self-Assembly of Mechanoplasmonic Bacterial Cellulose-Metal Nanoparticle Composites2020Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 30, nr 40, artikel-id 2004766Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Nanocomposites of metal nanoparticles (NPs) and bacterial nanocellulose (BC) enable fabrication of soft and biocompatible materials for optical, catalytic, electronic, and biomedical applications. Current BC-NP nanocomposites are typically prepared by in situ synthesis of the NPs or electrostatic adsorption of surface functionalized NPs, which limits possibilities to control and tune NP size, shape, concentration, and surface chemistry and influences the properties and performance of the materials. Here a self-assembly strategy is described for fabrication of complex and well-defined BC-NP composites using colloidal gold and silver NPs of different sizes, shapes, and concentrations. The self-assembly process results in nanocomposites with distinct biophysical and optical properties. In addition to antibacterial materials and materials with excellent senor performance, materials with unique mechanoplasmonic properties are developed. The homogenous incorporation of plasmonic gold NPs in the BC enables extensive modulation of the optical properties by mechanical stimuli. Compression gives rise to near-field coupling between adsorbed NPs, resulting in tunable spectral variations and enhanced broadband absorption that amplify both nonlinear optical and thermoplasmonic effects and enables novel biosensing strategies.

    Ladda ner fulltext (pdf)
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  • 17.
    Eskilson, Olof
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Zattarin, Elisa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Berglund, Linn
    Division of Materials Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, Luleå, Sweden.
    Oksman, Kristiina
    Division of Materials Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, Luleå, Sweden.
    Hanna, Kristina
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Rakar, Jonathan
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Sivlér, Petter
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Skog, Mårten
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rinklake, Ivana
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Shamasha, Rozalin
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Sotra, Zeljana
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Starkenberg, Annika
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Odén, Magnus
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Wiman, Emanuel
    Cardiovascular Research Centre, School of Medical Sciences, Örebro University, Örebro, Sweden.
    Khalaf, Hazem
    Cardiovascular Research Centre, School of Medical Sciences, Örebro University, Örebro, Sweden.
    Bengtsson, Torbjörn
    Cardiovascular Research Centre, School of Medical Sciences, Örebro University, Örebro, Sweden.
    Junker, Johan
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för kirurgi, ortopedi och onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Regionledningskontoret, Katastrofmedicinskt centrum.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Björk, Emma
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Nanocellulose composite wound dressings for real-time pH wound monitoring2023Ingår i: Materials Today Bio, ISSN 2590-0064, Vol. 19, artikel-id 100574Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The skin is the largest organ of the human body. Wounds disrupt the functions of the skin and can have catastrophic consequences for an individual resulting in significant morbidity and mortality. Wound infections are common and can substantially delay healing and can result in non-healing wounds and sepsis. Early diagnosis and treatment of infection reduce risk of complications and support wound healing. Methods for monitoring of wound pH can facilitate early detection of infection. Here we show a novel strategy for integrating pH sensing capabilities in state-of-the-art hydrogel-based wound dressings fabricated from bacterial nanocellulose (BC). A high surface area material was developed by self-assembly of mesoporous silica nanoparticles (MSNs) in BC. By encapsulating a pH-responsive dye in the MSNs, wound dressings for continuous pH sensing with spatiotemporal resolution were developed. The pH responsive BC-based nanocomposites demonstrated excellent wound dressing properties, with respect to conformability, mechanical properties, and water vapor transmission rate. In addition to facilitating rapid colorimetric assessment of wound pH, this strategy for generating functional BC-MSN nanocomposites can be further be adapted for encapsulation and release of bioactive compounds for treatment of hard-to-heal wounds, enabling development of novel wound care materials.

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  • 18.
    Eskilsson, Olof
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Kollenchery Ramanathan, Sneha
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Du Rietz, Anna
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär ytfysik och nanovetenskap. Linköpings universitet, Tekniska fakulteten.
    Guerrero Florez, Valentina
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Uvdal, Kajsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär ytfysik och nanovetenskap. Linköpings universitet, Tekniska fakulteten.
    Björk, Emma
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Self-Assembly of Metal Nanoparticles in Bacterial Cellulose for the Fabrication of Soft Substrate-Supported Catalysts2024Ingår i: ACS Applied Nano Materials, E-ISSN 2574-0970Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The transition to green and sustainable catalysts necessitates efficient and safe preparation techniques using abundant and renewable resources. Many metal nanoparticles (NPs) are excellent catalysts but suffer from poor colloidal stability. NP immobilization or fabrication of metal nanostructures on solid supports can avoid issues with NP aggregation and facilitate the reuse of catalysts, but it may result in a decrease in the catalytic performance of the NPs. Here, we show that well-defined colloidal silver, gold, and platinum NPs can be self-assembled in bacterial nanocellulose (BC) membranes, yielding BC-NP nanocomposites that are highly catalytically active using the reduction of 4-nitrophenol (4-NP) as a model reaction. The large effective surface area of BC enables the assembly of large quantities of NPs, resulting in materials with excellent catalytic performance. To address the mass transport limitations of reactants through the 3D nanofibrillar BC network, the membranes were dissociated using sonication to produce dispersed nanocellulose fibrils. This process dramatically reduced the time required for the adsorption of the NPs from days to minutes. Moreover, the catalytic performance of the nanofibril-supported NPs was drastically improved. A turnover frequency above 21,000 h(-1) was demonstrated, which is more than one order of magnitude higher than that for previously reported soft substrate-supported AuNP-based catalytic materials. The ease of fabrication, abundance, and low environmental footprint of the support material, along with reusability, stability, and unprecedented catalytic performance, make BC-NP nanocomposites a compelling option for green and sustainable catalysis.

  • 19.
    Fernandez-Benito, Amparo
    et al.
    CSIC, Spain.
    Martinez-Lopez, Juan Carlos
    CSIC, Spain.
    Jafari, Mohammad Javad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Solin, Niclas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Elektroniska och fotoniska material. Linköpings universitet, Tekniska fakulteten.
    Martinez Gil, Jose Gabriel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Garcia-Gimenez, Daniel
    CSIC, Spain.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Elektroniska och fotoniska material. Linköpings universitet, Tekniska fakulteten.
    Carretero-Gonzalez, Javier
    CSIC, Spain.
    Green and Scalable Biopolymer-Based Aqueous Polyelectrolyte Complexes for Zinc-Ion Charge Storage Devices2023Ingår i: ChemElectroChem, E-ISSN 2196-0216, Vol. 10, nr 2, artikel-id e202300327Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Green and scalable materials are essential to fulfill the need of electrification for transitioning into a fossil-fuels free society, and sustainability is a requirement for all new technologies. Rechargeable batteries are one of the most important elements for electrification, enabling the transition to mobile electronics, electrical vehicles and grid storage. We here report synthesis and characterization of polyelectrolyte complexes of alginate and chitosan, both biopolymers deriving from the sea, for transport of zinc ions in hydrogel electrolytes. We have used vibrational spectroscopy, thermal measurements and microscopy, as well as transport measurements with ohmic or blocking contacts. The transference number for zinc ions is close to 1, the conductivity is approximate to 10 mS/cm, with stability at Zn interfaces seen through 7000 cycles in symmetric zinc//zinc cell. A zinc ion aqueous electrolyte was prepared from blends of chitosan and alginate, by using a simple and scalable route. These green zinc ion electrolytes exhibit a stability window up to 2 V, a zinc ion transference number close to 1, and electrochemical cyclability over 7000 cycles at interfaces to zinc. This biologically derived polyelectrolyte complex offers many possibilities for optimizing transport and stability at electrode interfaces.image

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  • 20.
    Gamage, Sampath
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Kang, Evan
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Chungbuk Natl Univ, South Korea.
    Åkerlind, Christina
    FOI Swedish Def Res Agcy, S-58330 Linkoping, Sweden.
    Sardar, Samim
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Ist Italiano Tecnol, Italy.
    Edberg, Jesper
    RISE Acreo, Sweden.
    Kariis, Hans
    FOI Swedish Def Res Agcy, S-58330 Linkoping, Sweden.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Jonsson, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Transparent nanocellulose metamaterial enables controlled optical diffusion and radiative cooling2020Ingår i: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 8, nr 34, s. 11687-11694Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Materials that provide independent control of infrared thermal radiation and haze in the visible could benefit many areas and applications, including clothing, packaging and photovoltaics. Here, we study this possibility for a metamaterial composite paper based on cellulose nanofibrils (CNF) and silicon dioxide (SiO2) microparticles with infrared (IR) Frohlich phonon resonances. This CNF-SiO2 composite shows outstanding transparency in the visible wavelength range, with the option of controlling light diffusion and haze from almost zero to 90% by varying the SiO2 microparticle concentration. We further show that the transparent metamaterial paper could maintain high thermal emissivity in the atmospheric IR window, as attributed to strong IR absorption of both the nanocellulose and the resonant SiO2 microparticles. The high IR emissivity and low visible absorption make the paper suitable for passive radiative cooling and we demonstrate cooling of the paper to around 3 degrees C below ambient air temperature by exposing it to the sky.

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  • 21.
    Gavutis, Martynas
    et al.
    Ctr Phys Sci & Technol, Lithuania.
    Schulze-Niemand, Eric
    Max Planck Inst Dynam Complex Tech Syst, Germany; Otto von Guericke Univ, Germany.
    Lee, Hung-Hsun
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Liedberg, Bo
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Stein, Matthias
    Max Planck Inst Dynam Complex Tech Syst, Germany.
    Valiokas, Ramunas
    Ctr Phys Sci & Technol, Lithuania.
    Bilayer lipid membrane formation on surface assemblies with sparsely distributed tethers2023Ingår i: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 15, nr 22, s. 9759-9774Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A combined computational and experimental study of small unilamellar vesicle (SUV) fusion on mixed self-assembled monolayers (SAMs) terminated with different deuterated tether moieties (-(CD2)(7)CD3 or -(CD2)(15)CD3) is reported. Tethered bilayer lipid membrane (tBLM) formation of synthetic 1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine was initially probed on SAMs with controlled tether (d-alkyl tail) surface densities and lateral molecular packing using quartz crystal microbalance with dissipation monitoring (QCM-D). Long time-scale coarse-grained molecular dynamics (MD) simulations were then employed to elucidate the mechanisms behind the interaction between the SUVs and the different phases formed by the -(CD2)(7)CD3 and -(CD2)(15)CD3 tethers. Furthermore, a series of real time kinetics was recorded under different osmotic conditions using QCM-D to determine the accumulated lipid mass and for probing the fusion process. It is shown that the key factors driving the SUV fusion and tBLM formation on this type of surfaces involve tether insertion into the SUVs along with vesicle deformation. It is also evident that surface densities of the tethers as small as a few mol% are sufficient to obtain stable tBLMs with a high reproducibility. The described "sparsely tethered" tBLM system can be advantageous in studying different biophysical phenomena, such as membrane protein insertion, effects of receptor clustering, and raft formation.

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  • 22.
    Ghorbani Shiraz, Hamid
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ruoko, Tero-Petri
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Tampere Univ, Finland.
    Gueskine, Viktor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Karon, Krzysztof
    Silesian Tech Univ, Poland.
    Lapkowski, Mieczyslaw
    Silesian Tech Univ, Poland.
    Abrahamsson, Tobias
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Towards electrochemical hydrogen storage in liquid organic hydrogen carriers via proton-coupled electron transfers2022Ingår i: Journal of Energy Challenges and Mechanics, E-ISSN 2056-9386, Vol. 73, s. 292-300Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Green hydrogen is identified as one of the prime clean energy carriers due to its high energy density and a zero emission of CO2. A possible solution for the transport of H2 in a safe and low-cost way is in the form of liquid organic hydrogen carriers (LOHCs). As an alternative to loading LOHC with H2 via a two-step procedure involving preliminary electrolytic production of H2 and subsequent chemical hydrogenation of the LOHC, we explore here the possibility of electrochemical hydrogen storage (EHS) via conversion of proton of a proton donor into a hydrogen atom involved in covalent bonds with the LOHC (R) via a protoncoupled electron transfer (PCET) reaction: . We chose 9-fluorenone/ fluorenol (Fnone/Fnol) conversion as such a model PCET reaction. The electrochemical activation of Fnone via two sequential electron transfers was monitored with in-situ and operando spectroscopies in absence and in presence of different alcohols as proton donors of different reactivity, which enabled us to both quantify and get the mechanistic insight on PCET. The possibility of hydrogen extraction from the loaded carrier molecule was illustrated by chemical activation.

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  • 23.
    Guell-Grau, Pau
    et al.
    Inst Microelect Barcelona IMBCNM CSIC, Spain; CSIC, Spain; BIST, Spain; Networking Res Ctr Bioengn Biomat & Nanomed CIBER, Spain.
    Pi, Francesc
    Univ Autonoma Barcelona, Spain.
    Villa, Rosa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Inst Microelect Barcelona IMBCNM CSIC, Spain; Networking Res Ctr Bioengn Biomat & Nanomed CIBER, Spain.
    Eskilson, Olof
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Nogues, Josep
    CSIC, Spain; BIST, Spain; ICREA, Spain.
    Sepulveda, Borja
    Inst Microelect Barcelona IMBCNM CSIC, Spain.
    Alvarez, Mar
    Inst Microelect Barcelona IMBCNM CSIC, Spain.
    Elastic Plasmonic-Enhanced Fabry-Perot Cavities with Ultrasensitive Stretching Tunability2022Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 34, nr 7, artikel-id 2106731Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The emerging stretchable photonics field faces challenges, like the robust integration of optical elements into elastic matrices or the generation of large optomechanical effects. Here, the first stretchable plasmonic-enhanced and wrinkled Fabry-Perot (FP) cavities are demonstrated, which are composed of self-embedded arrays of Au nanostructures at controlled depths into elastomer films. The novel self-embedding process is triggered by the Au nanostructures catalytic activity, which locally increases the polymer curing rate, thereby inducing a mechanical stress that simultaneously pulls the Au nanostructures into the polymer and forms a wrinkled skin layer. This geometry yields unprecedented optomechanical effects produced by the coupling of the broad plasmonic modes of the Au nanostructures and the FP modes, which are modulated by the wrinkled optical cavity. As a result, film stretching induces drastic changes in both the spectral position and intensity of the plasmonic-enhanced FP resonances due to the simultaneous cavity thickness reduction and cavity wrinkle flattening, thus increasing the cavity finesse. These optomechanical effects are exploited to demonstrate new strain-sensing approaches, achieving a strain detection limit of 0.006%, i.e., 16-fold lower than current optical strain-detection schemes.

  • 24.
    Guerrero-Barajas, Claudia
    et al.
    Inst Politecn Nacl, Mexico.
    Constantino-Salinas, Erick A.
    Inst Politecn Nacl, Mexico.
    Amora-Lazcano, Enriqueta
    Inst Politecn Nacl, Mexico.
    Tlalapango-Angeles, Daniel
    Inst Politecn Nacl, Mexico.
    Mendoza Figueroa, Silvestre
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Inst Politecn Nacl, Mexico.
    Cruz-Maya, Juan A.
    Inst Politecn Nacl, Mexico.
    Jan-Roblero, Janet
    Inst Politecn Nacl, Mexico.
    Bacillus mycoides A1 and Bacillus tequilensis A3 inhibit the growth of a member of the phytopathogen Colletotrichum gloeosporioides species complex in avocado2020Ingår i: Journal of the Science of Food and Agriculture, ISSN 0022-5142, E-ISSN 1097-0010, Vol. 100, s. 4049-4056Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    BACKGROUND Avocado is affected by Colletotrichum gloeosporioides causing anthracnose. Antagonistic microorganisms against C. gloeosporioides represent an alternative for biological control. Accordingly, in the present study, we focused on the isolation and characterization of potential antagonist bacteria against a member of the C. gloeosporioides species complex with respect to their possible future application. RESULTS Samples of avocado rhizospheric soil were aquired from an orchard located in Ocuituco, Morelos, Mexico, aiming to obtain bacterial isolates with potential antifungal activity. From the soil samples, 136 bacteria were isolated and they were then challenged against a member of the C. gloeosporioides species complex; only three bacterial isolates A1, A2 and A3 significantly diminished mycelial fungal growth by 75%, 70% and 60%, respectively. Two of these isolates were identified by 16S rRNA as Bacillus mycoides (A1 and A2) and the third was identified as Bacillus tequilensis (A3). Bacillus mycoides bacterial cell-free supernatant reduced the mycelial growth of a member of the C. gloeosporioides species complex isolated from avocado by 65%, whereas Bacillus tequilensis A3 supernatant did so by 25% after 3 days post inoculation. Bacillus tequilensis mycoides A1 was a producer of proteases, indolacetic acid and siderophores. Preventive treatment using a cell-free supernatant of B. mycoides A1 diminished the severity of anthracnose disease (41.9%) on avocado fruit. CONCLUSION These results reveal the possibility of using B. mycoides A1 as a potential biological control agent. (c) 2020 Society of Chemical Industry

  • 25.
    Iversen, Alexandra
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Utterström, Johanna
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Enzymatically Triggered Peptide–Lipid Conjugation of Designed Membrane Active Peptides for Controlled Liposomal Release2024Ingår i: ACS Omega, Vol. 9, nr 17, s. 19613-19619Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Possibilities for controlling the release of pharmaceuticals from liposomal drug delivery systems can enhance their efficacy and reduce their side effects. Membrane-active peptides (MAPs) can be tailored to promote liposomal release when conjugated to lipid head groups using thiol-maleimide chemistry. However, the rapid oxidation of thiols hampers the optimization of such conjugation-dependent release strategies. Here, we demonstrate a de novo designed MAP modified with an enzyme-labile Cys-protection group (phenylacetamidomethyl (Phacm)) that prevents oxidation and facilitates in situ peptide lipidation. Before deprotection, the peptide lacks a defined secondary structure and does not interact with maleimide-functionalized vesicles. After deprotection of Cys using penicillin G acylase (PGA), the peptide adopts an α-helical conformation and triggers rapid release of vesicle content. Both the peptide and PGA concentrations significantly influence the conjugation process and, consequently, the release kinetics. At a PGA concentration of 5 μM the conjugation and release kinetics closely mirror those of fully reduced, unprotected peptides. We anticipate that these findings will enable further refinement of MAP conjugation and release processes, facilitating the development of sophisticated bioresponsive MAP-based liposomal drug delivery systems.

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  • 26.
    Jafari, Mohammad Javad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Backlund, Fredrik G.
    Karolinska Inst, Sweden; RISE Res Inst Sweden, Sweden.
    Arndt, Tina
    Karolinska Inst, Sweden.
    Schmuck, Benjamin
    Karolinska Inst, Sweden; Swedish Univ Agr Sci, Sweden.
    Greco, Gabriele
    Swedish Univ Agr Sci, Sweden.
    Rising, Anna
    Karolinska Inst, Sweden; Swedish Univ Agr Sci, Sweden.
    Barth, Andreas
    Stockholm Univ, Sweden.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Force-Induced Structural Changes in Spider Silk Fibers Introduced by ATR-FTIR Spectroscopy2023Ingår i: ACS APPLIED POLYMER MATERIALS, ISSN 2637-6105, Vol. 5, nr 11, s. 9433-9444Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Silk fibers have unique mechanical properties, and many studies of silk aim at understanding how these properties are related to secondary structure content, which often is determined by infrared spectroscopy. We report significant method-induced irreversible structural changes to both natural and synthetic spider silk fibers, derived from the widely used attenuated total reflection Fourier-transform infrared (ATR-FTIR) technique. By varying the force used to bring fibers into contact with the internal reflection elements of ATR-FTIR accessories, we observed correlated and largely irreversible changes in the secondary structure, with shape relaxation under pressure occurring within minutes. Fitting of spectral components shows that these changes agree with transformations from the alpha-helix to the beta-sheet secondary structure with possible contributions from other secondary structure elements. We further confirm the findings with IR microspectroscopy, where similar differences were seen between the pressed and unaffected regions of spider silk fibers. Our findings show that ATR-FTIR spectroscopy requires care in its use and in the interpretation of the results.

  • 27.
    Jafari, Mohammad Javad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Golabi, Mohsen
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten. Univ Isfahan, Iran.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Antimicrobial susceptibility testing using infrared attenuated total reflection (IR-ATR) spectroscopy to monitor metabolic activity2024Ingår i: Spectrochimica Acta Part A - Molecular and Biomolecular Spectroscopy, ISSN 1386-1425, E-ISSN 1873-3557, Vol. 304, artikel-id 123384Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Fast and accurate detection of antimicrobial resistance in pathogens remains a challenge, and with the increase in antimicrobial resistance due to mis- and overuse of antibiotics, it has become an urgent public health problem. We demonstrate how infrared attenuated total reflection (IR-ATR) can be used as a simple method for assessment of bacterial susceptibility to antibiotics. This is achieved by monitoring the metabolic activities of bacterial cells via nutrient consumption and using this as an indicator of bacterial viability. Principal component analysis of the obtained spectra provides a tool for fast and simple discrimination of antimicrobial resistance in the acquired data. We demonstrate this concept using four bacterial strains and four different antibiotics, showing that the change in glucose concentration in the growth medium after 2 h, as monitored by IR-ATR, can be used as a spectroscopic diagnostic technique, to reduce detection time and to improve quality in the assessment of antimicrobial resistance in pathogens.

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  • 28.
    Jafari, Mohammad Javad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Oshaug Pedersen, Jonas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Barhemat, Samira
    Mabema AB, Dept Vis Inspect, S-58422 Linkoping, Sweden.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    In Situ Surface-Enhanced Raman Spectroscopy on Organic Mixed Ionic-Electronic Conductors: Tracking Dynamic Doping in Light-Emitting Electrochemical Cells2024Ingår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In the domain of organic mixed ionic-electronic conductors (OMIECs), simultaneous transport and coupling of ionic and electronic charges are crucial for the function of electrochemical devices in organic electronics. Understanding conduction mechanisms and chemical reactions in operational devices is pivotal for performance enhancement and is necessary for the informed and systematic development of more promising materials. Surface-enhanced Raman spectroscopy (SERS) is a potent tool for monitoring electrochemical evolution and dynamic doping in operational devices, offering enhanced sensitivity to subtle spectral changes. We demonstrate the utility of SERS for in situ tracking of doping in OMIECs in an organic light-emitting electrochemical cell (LEC) containing a conjugated polymer (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]; MEH-PPV), a molecular anion (lithium triflate), and an electrolyte network (poly(ethylene oxide); PEO). SERS enhancement is achieved via an interleaved layer of gold particles formed by spontaneous breakup of a deposited thin gold film. The results successfully highlight the ability of SERS to unveil time-resolved MEH-PPV doping and polaron formation, elucidating the effects of triflate ion transfer in the operating device and validating the electrochemical doping model in LECs.

  • 29.
    Jafari, Mohammad Javad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rogström, Lina
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Andersson, Jon M.
    SECO Tools AB, Sweden.
    Birch, Jens
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tunnfilmsfysik. Linköpings universitet, Tekniska fakulteten.
    Gibmeier, Jens
    Karlsruhe Inst Technol KIT, Germany.
    Joesaar, Mats J.
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten. SECO Tools AB, Sweden.
    Kiefer, Dominik
    Karlsruhe Inst Technol KIT, Germany.
    Odén, Magnus
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Nanostrukturerade material. Linköpings universitet, Tekniska fakulteten.
    Thermal degradation of TiN and TiAlN coatings during rapid laser treatment2021Ingår i: Surface & Coatings Technology, ISSN 0257-8972, E-ISSN 1879-3347, Vol. 422, artikel-id 127517Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In this research, a fundamental study was conducted on damage behavior of cathodic arc evaporated TiN and Ti0.44Al0.56N coatings, in terms of oxidation and cracking/spallation, when they were exposed to single-pulse laser treatment in a temperature range of 1200-2100 degrees C. Moreover, a multiple-pulse laser treatment was designed to apply thermo-mechanical loads on the coatings in order to evaluate their thermal degradation during rapid heating/cooling cycles between 200 and 1200 degrees C. Single-pulse treatment of TiN up to 1500 degrees C led to the intercolumnar cracking and formation of ultrafine TiO grains. An increase in temperature up to 2100 degrees C resulted in a notable bulging of the surface, and formation of TiO2 of various morphologies such as grainy structure, dense molten and re-solidified structure, droplets from melt expulsion and, more interestingly, nanofibers. Multiplepulse treatment of TiN was accompanied by a severe cracking and spallation, which divided the surface into two layers: a heavily cracked top layer composed of dense TiO2 grains, and a bottom layer having porous TiO2 grains indicating incomplete oxidation. Conversely, Ti0.44Al0.56N did not show any visible cracking and oxidation after single-pulse treatment. Multiple-pulse treatment did not also yield cracking and spallation for Ti0.44Al0.56N, and its ablated region consisted of TiO2 grains combined with thin Al2O3 platelets. An excellent combination of properties including higher oxidation resistance and greater fracture toughness at high temperatures led to a higher thermal damage resistance for Ti0.44Al0.56N coating compared to TiN when undergoing single- and multiple-pulse laser treatments.

  • 30.
    Ji, Fuxiang
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Klarbring, Johan
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk Fysik. Linköpings universitet, Tekniska fakulteten.
    Wang, Feng
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Ning, Weihua
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Wang, Linqin
    KTH Royal Inst Technol, Sweden.
    Yin, Chunyang
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Mendoza Figueroa, José Silvestre
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Christensen, Christian Kolle
    DESY, Germany.
    Etter, Martin
    DESY, Germany.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Sun, Licheng
    KTH Royal Inst Technol, Sweden; Dalian Univ Technol, Peoples R China.
    Simak, Sergey
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk Fysik. Linköpings universitet, Tekniska fakulteten.
    Abrikosov, Igor
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk Fysik. Linköpings universitet, Tekniska fakulteten. Natl Univ Sci and Technol MISIS, Russia.
    Gao, Feng
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Lead-Free Halide Double Perovskite Cs2AgBiBr6with Decreased Band Gap2020Ingår i: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 59, nr 35, s. 15191-15194Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Environmentally friendly halide double perovskites with improved stability are regarded as a promising alternative to lead halide perovskites. The benchmark double perovskite, Cs2AgBiBr6, shows attractive optical and electronic features, making it promising for high-efficiency optoelectronic devices. However, the large band gap limits its further applications, especially for photovoltaics. Herein, we develop a novel crystal-engineering strategy to significantly decrease the band gap by approximately 0.26 eV, reaching the smallest reported band gap of 1.72 eV for Cs(2)AgBiBr(6)under ambient conditions. The band-gap narrowing is confirmed by both absorption and photoluminescence measurements. Our first-principles calculations indicate that enhanced Ag-Bi disorder has a large impact on the band structure and decreases the band gap, providing a possible explanation of the observed band-gap narrowing effect. This work provides new insights for achieving lead-free double perovskites with suitable band gaps for optoelectronic applications.

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  • 31.
    Jury, Michael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Modular Hyaluronan-Based Hydrogels for 3D Cell Culture and Bioprinting2022Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
    Abstract [en]

    Three-dimensional (3D) cell culture facilitates development of biological relevant assays for drug screening and toxicity testing. Compared to conventional 2D cell culture, cells cultured in 3D can more accurately mimic human tissues and organs and thus provide ex vivo data with potentially better predictive value for cancer research, pharmacology, and toxicology, reducing the need for animal models, improving experimental reproducibility, and reducing time and costs in drug development. The most widely used options for scaffold-based 3D cell culture are, however, based on poorly defined biologically derived extracellular matrix (ECM) with limited possibilities to tailor material properties and that are difficult to combine with state-of-the art biofabrication techniques.   

    The overall aim this thesis was to design and explore modular hyaluronan (HA) based ECM-mimicking hydrogels with tuneable physiochemical properties and biofunctionalities, for development of advanced 3D cell models and biofabrication. The thesis work is presented in five papers. In paper I, we used copper free click chemistry for both hydrogel cross-linking and functionalization with fibronectin derived peptide sequences for culture of human induced pluripotent-derived hepatocytes in a perfused microfluidic system. The tuneable and bioorthogonal cross-linking enabled both retention of high cell viabilities and fabrication of a functional liver-on-chip solution. In paper II, we combined the developed HA-based hydrogel system with homo- and heterodimerizing helix-loop-helix peptides for modulation of both cross-linking density and biofunctionalization. We further demonstrated the possibilities to use these hydrogels as bioinks for 3D bioprinting where both the molecular composition and the physical properties of the printed structures could be dynamically altered, providing new avenues for four-dimensional (4D) bioprinting. In paper III we investigated the possibilities to chemically conjugate full size recombinant human laminin-521 (LN521) in the HA-based hydrogels system using copper-free click chemistry, with the aim to enable 3D culture and 3D bioprinting of neurons. We quantified the impact of using different linkers to tether LN521 and the influence of LN-functionalization on the structural and mechanical properties of the hydrogels. We show that both differentiated and non-differentiated neuroblastoma cells and long-term self-renewing neuroepithelial stem cells (lt-NES) remained viable in the hydrogels. The hydrogels also had a protected effect on lt-NES during syringe ejection and bioprinting. In paper IV, we used HA-based hydrogels modified with peptides sequences derived from fibronectin and laminin for culture of fetal primary astrocytes (FPA). We explored both the interactions between the hydrogels and FPA and possibilities to 3D bioprint FPAs.  Finally, in paper V, we developed HA-nanocellulose composite hydrogels with the aim to increase printing fidelity and enable fabrication of multi-layered bioprinted structures without the use of a support bath. In addition to HA, we used wood-fibre derived nanocellulose (NC) to increase the viscosity of the bioink during the printing process.  

    The developed biorthogonal and modular hydrogel systems provide a large degree of flexibility that allows for encapsulation and culture of different cell types and processing using different techniques, which can contribute to further exploration of fabrication of biologically relevant tissue and disease models.   

    Delarbeten
    1. Fabrication of modular hyaluronan-PEG hydrogels to support 3D cultures of hepatocytes in a perfused liver-on-a-chip device
    Öppna denna publikation i ny flik eller fönster >>Fabrication of modular hyaluronan-PEG hydrogels to support 3D cultures of hepatocytes in a perfused liver-on-a-chip device
    Visa övriga...
    2019 (Engelska)Ingår i: Biofabrication, ISSN 1758-5082, E-ISSN 1758-5090, Vol. 11, nr 1, s. 1-13, artikel-id 015013Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Liver cell culture models are attractive in both tissue engineering and for development of assays for drug toxicology research. To retain liver specific cell functions, the use of adequate cell types and culture conditions, such as a 3D orientation of the cells and a proper supply of nutrients and oxygen, are critical. In this article, we show how extracellular matrix mimetic hydrogels can support hepatocyte viability and functionality in a perfused liver-on-a-chip device. A modular hydrogel system based on hyaluronan and poly(ethylene glycol) (HA-PEG), modified with cyclooctyne moieties for bioorthogonal strain-promoted alkyne-azide 1, 3-dipolar cycloaddition (SPAAC), was developed, characterized, and compared for cell compatibility to hydrogels based on agarose and alginate. Hepatoma cells (HepG2) formed spheroids with viable cells in all hydrogels with the highest expression of albumin and urea in alginate hydrogels. By including an excess of cyclooctyne in the HA backbone, azide-modified cell adhesion motifs (linear and cyclic RGD peptides) could be introduced in order to enhance viability and functionality of human induced pluripotent stem cell derived hepatocytes (hiPS-HEPs). In the HA-PEG hydrogels modified with cyclic RGD peptides hiPS-HEPs migrated and grew in 3D and showed an increased viability and higher albumin production compared to when cultured in the other hydrogels. This flexible SPAAC crosslinked hydrogel system enabled fabrication of perfused 3D cell culture of hiPS-HEPs and is a promising material for further development and optimization of liver-on-a-chip devices.

    Ort, förlag, år, upplaga, sidor
    Institute of Physics (IOP), 2019
    Nationell ämneskategori
    Cell- och molekylärbiologi Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci) Cellbiologi
    Identifikatorer
    urn:nbn:se:liu:diva-154008 (URN)10.1088/1758-5090/aaf657 (DOI)000454550900002 ()
    Tillgänglig från: 2019-01-22 Skapad: 2019-01-22 Senast uppdaterad: 2022-04-29Bibliografiskt granskad
    2. Dynamic peptide-folding mediated biofunctionalization and modulation of hydrogels for 4D bioprinting
    Öppna denna publikation i ny flik eller fönster >>Dynamic peptide-folding mediated biofunctionalization and modulation of hydrogels for 4D bioprinting
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    2020 (Engelska)Ingår i: Biofabrication, ISSN 1758-5082, E-ISSN 1758-5090, Vol. 12, nr 3, artikel-id 035031Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Hydrogels are used in a wide range of biomedical applications, including three-dimensional (3D) cell culture, cell therapy and bioprinting. To enable processing using advanced additive fabrication techniques and to mimic the dynamic nature of the extracellular matrix (ECM), the properties of the hydrogels must be possible to tailor and change over time with high precision. The design of hydrogels that are both structurally and functionally dynamic, while providing necessary mechanical support is challenging using conventional synthesis techniques. Here, we show a modular and 3D printable hydrogel system that combines a robust but tunable covalent bioorthogonal cross-linking strategy with specific peptide-folding mediated interactions for dynamic modulation of cross-linking and functionalization. The hyaluronan-based hydrogels were covalently cross-linked by strain-promoted alkyne-azide cycloaddition using multi-arm poly(ethylene glycol). In addition, ade novodesigned helix-loop-helix peptide was conjugated to the hyaluronan backbone to enable specific peptide-folding modulation of cross-linking density and kinetics, and hydrogel functionality. An array of complementary peptides with different functionalities was developed and used as a toolbox for supramolecular tuning of cell-hydrogel interactions and for controlling enzyme-mediated biomineralization processes. The modular peptide system enabled dynamic modifications of the properties of 3D printed structures, demonstrating a novel route for design of more sophisticated bioinks for four-dimensional bioprinting.

    Ort, förlag, år, upplaga, sidor
    IOP PUBLISHING LTD, 2020
    Nyckelord
    hydrogel; hyaluronan; peptide; folding; bioprinting; biomineralization
    Nationell ämneskategori
    Cell- och molekylärbiologi
    Identifikatorer
    urn:nbn:se:liu:diva-168253 (URN)10.1088/1758-5090/ab9490 (DOI)000548339700001 ()32428894 (PubMedID)
    Anmärkning

    Funding Agencies|Swedish Foundation for Strategic Research (SFF)Swedish Foundation for Strategic Research [FFL15-0026]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Carl Tryggers Foundation [CTS15:7, CTS18:5]; Knut and Alice Wallenberg FoundationKnut & Alice Wallenberg Foundation [KAW 2016.0231]

    Tillgänglig från: 2020-08-22 Skapad: 2020-08-22 Senast uppdaterad: 2024-02-07
    3. Bioorthogonally Cross-Linked Hyaluronan-Laminin Hydrogels for 3D Neuronal Cell Culture and Biofabrication
    Öppna denna publikation i ny flik eller fönster >>Bioorthogonally Cross-Linked Hyaluronan-Laminin Hydrogels for 3D Neuronal Cell Culture and Biofabrication
    Visa övriga...
    2022 (Engelska)Ingår i: Advanced Healthcare Materials, ISSN 2192-2640, E-ISSN 2192-2659, Vol. 11, nr 11, artikel-id 2102097Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Laminins (LNs) are key components in the extracellular matrix of neuronal tissues in the developing brain and neural stem cell niches. LN-presenting hydrogels can provide a biologically relevant matrix for the 3D culture of neurons toward development of advanced tissue models and cell-based therapies for the treatment of neurological disorders. Biologically derived hydrogels are rich in fragmented LN and are poorly defined concerning composition, which hampers clinical translation. Engineered hydrogels require elaborate and often cytotoxic chemistries for cross-linking and LN conjugation and provide limited possibilities to tailor the properties of the materials. Here a modular hydrogel system for neural 3D cell cultures, based on hyaluronan and poly(ethylene glycol), that is cross-linked and functionalized with human recombinant LN-521 using bioorthogonal copper-free click chemistry, is shown. Encapsulated human neuroblastoma cells demonstrate high viability and grow into spheroids. Long-term neuroepithelial stem cells (lt-NES) cultured in the hydrogels can undergo spontaneous differentiation to neural fate and demonstrate significantly higher viability than cells cultured without LN. The hydrogels further support the structural integrity of 3D bioprinted structures and maintain high viability of bioprinted and syringe extruded lt-NES, which can facilitate biofabrication and development of cell-based therapies.

    Ort, förlag, år, upplaga, sidor
    John Wiley & Sons, 2022
    Nyckelord
    3D bioprinting; 3D cell cultures; hyaluronan; hydrogels; laminin; neural stem cells
    Nationell ämneskategori
    Biofysik
    Identifikatorer
    urn:nbn:se:liu:diva-183407 (URN)10.1002/adhm.202102097 (DOI)000758054400001 ()35114074 (PubMedID)2-s2.0-85124817683 (Scopus ID)
    Anmärkning

    Funding Agencies: Swedish Foundation for Strategic Research (SFF) [FFL15-0026]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University [2009-00971]; Carl Tryggers Foundation; Knut and Alice Wallenberg Foundation [KAW 2016.0231, 2020.0206]

    Tillgänglig från: 2022-03-07 Skapad: 2022-03-07 Senast uppdaterad: 2023-10-24Bibliografiskt granskad
  • 32.
    Jury, Michael
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Matthiesen, Isabelle
    KTH Royal Institute of Technology, Stockholm, Sweden.
    Boroojeni, Fatemeh Rasti
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Ludwig, Saskia L.
    KTH Royal Institute of Technology, Stockholm, Sweden.
    Civitelli, Livia
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. University of Oxford, England.
    Winkler, Thomas E.
    KTH Royal Institute of Technology, Stockholm, Sweden; Institute of Microtechnology, Center of Pharmaceutical Engineering, Technische Universität Braunschweig, Braunschweig, Germany.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Herland, Anna
    Division of Micro and Nanosystems, KTH Royal Institute of Technology, Stockholm, Sweden; Department of Neuroscience, Karolinska Institute, Solna, Sweden; Division of Nanobiotechnology, Department of Protein Science, Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Bioorthogonally Cross-Linked Hyaluronan-Laminin Hydrogels for 3D Neuronal Cell Culture and Biofabrication2022Ingår i: Advanced Healthcare Materials, ISSN 2192-2640, E-ISSN 2192-2659, Vol. 11, nr 11, artikel-id 2102097Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Laminins (LNs) are key components in the extracellular matrix of neuronal tissues in the developing brain and neural stem cell niches. LN-presenting hydrogels can provide a biologically relevant matrix for the 3D culture of neurons toward development of advanced tissue models and cell-based therapies for the treatment of neurological disorders. Biologically derived hydrogels are rich in fragmented LN and are poorly defined concerning composition, which hampers clinical translation. Engineered hydrogels require elaborate and often cytotoxic chemistries for cross-linking and LN conjugation and provide limited possibilities to tailor the properties of the materials. Here a modular hydrogel system for neural 3D cell cultures, based on hyaluronan and poly(ethylene glycol), that is cross-linked and functionalized with human recombinant LN-521 using bioorthogonal copper-free click chemistry, is shown. Encapsulated human neuroblastoma cells demonstrate high viability and grow into spheroids. Long-term neuroepithelial stem cells (lt-NES) cultured in the hydrogels can undergo spontaneous differentiation to neural fate and demonstrate significantly higher viability than cells cultured without LN. The hydrogels further support the structural integrity of 3D bioprinted structures and maintain high viability of bioprinted and syringe extruded lt-NES, which can facilitate biofabrication and development of cell-based therapies.

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  • 33.
    Kim, Joochan
    et al.
    Sungkyunkwan Univ SKKU, South Korea.
    Jeon, Jaehyung
    Sungkyunkwan Univ SKKU, South Korea.
    Jang, Hyowon
    Korea Res Inst Biosci & Biotechnol KRIBB, South Korea.
    Moon, Youngkwang
    Sungkyunkwan Univ SKKU, South Korea.
    Abafogi, Abdurhaman Teyib
    Sungkyunkwan Univ SKKU, South Korea.
    van Noort, Danny
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Lee, Jinkee
    Sungkyunkwan Univ SKKU, South Korea; Sungkyunkwan Univ SKKU, South Korea.
    Kang, Taejoon
    Korea Res Inst Biosci & Biotechnol KRIBB, South Korea; Sungkyunkwan Univ SKKU, South Korea.
    Park, Sungsu
    Sungkyunkwan Univ SKKU, South Korea; Sungkyunkwan Univ SKKU, South Korea.
    3D printed fluidic swab for COVID-19 testing with improved diagnostic yield and user comfort2023Ingår i: NANO CONVERGENCE, ISSN 2196-5404, Vol. 10, nr 1, artikel-id 45Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The current standard method of diagnosing coronavirus disease 2019 (COVID-19) involves uncomfortable and invasive nasopharyngeal (NP) sampling using cotton swabs (CS), which can be unsuitable for self-testing. Although mid-turbinate sampling is an alternative, it has a lower diagnostic yield than NP sampling. Nasal wash (NW) has a similar diagnostic yield to NP sampling, but is cumbersome to perform. In this study, we introduce a 3D printed fluidic swab (3DPFS) that enables easy NW sampling for COVID-19 testing with improved diagnostic yield. The 3DPFS comprises a swab head, microchannel, and socket that can be connected to a syringe containing 250 & mu;L of NW solution. The 3DPFS efficiently collects nasal fluid from the surface of the nasal cavity, resulting in higher sensitivity than CS for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This was confirmed by both reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and lateral flow assays (LFA) in virus-spiked nasal samples and clinical samples. Additionally, users reported greater comfort when using the 3DPFS compared to CS. These findings suggest that the 3DPFS can improve the performance of COVID-19 testing by facilitating efficient and less painful nasal sample collection.

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  • 34.
    Kim, Min-Hyeok
    et al.
    School of Mechanical Engineering, Sungkyunkwan University (SKKU), Suwon, Korea.
    van Noort, Danny
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten. Centro de Investigación en Bioingeniería, Universidad de Ingenieria y Tecnologia—UTEC, Lima, Peru.
    Sung, Jong Hwan
    Department of Chemical Engineering, Hongik University, Seoul, Korea.
    Park, Sungsu
    School of Mechanical Engineering, Sungkyunkwan University (SKKU), Suwon, Korea; Department of Biophysics, Institute of Quantum Biophysics (IQB), Sungkyunkwan University (SKKU), Suwon, Korea.
    Organ-on-a-Chip for Studying Gut-Brain Interaction Mediated by Extracellular Vesicles in the Gut Microenvironment2021Ingår i: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, Vol. 22, nr 24, artikel-id 13513Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    Extracellular vesicles (EVs) are a group of membrane vesicles that play important roles in cell-to-cell and interspecies/interkingdom communications by modulating the pathophysiological conditions of recipient cells. Recent evidence has implied their potential roles in the gut-brain axis (GBA), which is a complex bidirectional communication system between the gut environment and brain pathophysiology. Despite the evidence, the roles of EVs in the gut microenvironment in the GBA are less highlighted. Moreover, there are critical challenges in the current GBA models and analyzing techniques for EVs, which may hinder the research. Currently, advances in organ-on-a-chip (OOC) technologies have provided a promising solution. Here, we review the potential effects of EVs occurring in the gut environment on brain physiology and behavior and discuss how to apply OOCs to research the GBA mediated by EVs in the gut microenvironment.

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  • 35.
    Kim, Nara
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Lienemann, Samuel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Petsagkourakis, Ioannis
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Mengistie, Desalegn
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Calif Polytech State Univ San Luis Obispo, CA 93407 USA.
    Kee, Seyoung
    Univ Auckland, New Zealand.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Gueskine, Viktor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Leclere, Philippe
    Univ Mons, Belgium.
    Lazzaroni, Roberto
    Univ Mons, Belgium.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Tybrandt, Klas
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Elastic conducting polymer composites in thermoelectric modules2020Ingår i: Nature Communications, E-ISSN 2041-1723, Vol. 11, nr 1Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The rapid growth of wearables has created a demand for lightweight, elastic and conformal energy harvesting and storage devices. The conducting polymer poly(3,4-ethylenedioxythiophene) has shown great promise for thermoelectric generators, however, the thick layers of pristine poly(3,4-ethylenedioxythiophene) required for effective energy harvesting are too hard and brittle for seamless integration into wearables. Poly(3,4-ethylenedioxythiophene)-elastomer composites have been developed to improve its mechanical properties, although so far without simultaneously achieving softness, high electrical conductivity, and stretchability. Here we report an aqueously processed poly(3,4-ethylenedioxythiophene)-polyurethane-ionic liquid composite, which combines high conductivity (>140Scm(-1)) with superior stretchability (>600%), elasticity, and low Youngs modulus (<7MPa). The outstanding performance of this organic nanocomposite is the result of favorable percolation networks on the nano- and micro-scale and the plasticizing effect of the ionic liquid. The elastic thermoelectric material is implemented in the first reported intrinsically stretchable organic thermoelectric module. Though deformable thermoelectric materials are desirable for integrating thermoelectric devices into wearable electronics, typical thermoelectric materials are too brittle for practical application. Here, the authors report a high-performance elastic composite for stretchable thermoelectric modules.

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  • 36.
    Lander, Sanna
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Cellfion AB, Sweden.
    Pang, Jiu
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Erlandsson, Johan
    Linköpings universitet. Cellfion AB, Sweden.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Jafari, Mohammad Javad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Korhonen, Leena
    BillerudKorsnas AB, Sweden.
    Yang, Hongli
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Abrahamsson, Tobias
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ding, Penghui
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Gueskine, Viktor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Mehandzhiyski, Alexandar
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Wågberg, Lars
    Linköpings universitet. KTH Royal Inst Technol, Sweden.
    Crispin, Reverant
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Controlling the rate of posolyte degradation in all-quinone aqueous organic redox flow batteries by sulfonated nanocellulose based membranes: The role of crossover and Michael addition2024Ingår i: Journal of Energy Storage, ISSN 2352-152X, E-ISSN 2352-1538, Vol. 83, artikel-id 110338Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Aqueous organic redox flow battery (AORFB) is a technological route towards the large-scale sustainable energy storage. However, several factors need to be controlled to maintain the AORFB performance. Prevention of posolyte and negolyte cross-contamination in asymmetric AORFBs, one of the main causes of capacity decay, relies on their membranes' ability to prevent migration of the redox-active species between the two electrolytes. The barrier properties are often traded for a reduction in ionic conductivity which is crucial to enable the device operation. Another factor greatly affecting quinone-based AORFBs is the Michael addition reaction (MAR) on the charged posolyte, quinone, which has been identified as a major reason for all-quinone AORFBs performance deterioration. Herein, we investigate deterioration scenarios of an all-quinone AORFB using both experimental and computational methods. The study includes a series of membranes based on sulfonated cellulose nanofibrils and different membrane modifications. The layer-by-layer (LbL) surface modifications, i.e. the incorporation of inorganic materials and the reduction of the pore size of the sulfonated cellulose membranes, were all viable routes to reduce the passive diffusion permeability of membranes which correlated to an increased cycling stability of the battery. The kinetics of MAR on quinone was detected using NMR and its impact on the performance fading was modeled computationally. The localization of MAR close to the membrane, which can be assigned to the surface reactivity, affects the diffusion of MAR reagent and the deterioration dynamics of the present all-quinone AORFB.

  • 37.
    Lefevre, Mathilde
    et al.
    Univ Mons, Belgium; Univ Mons, Belgium.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Masai, Thibault
    Univ Mons, Belgium.
    Wattiez, Ruddy
    Univ Mons, Belgium.
    Leclere, Philippe
    Univ Mons, Belgium.
    Flammang, Patrick
    Univ Mons, Belgium.
    Hennebert, Elise
    Univ Mons, Belgium.
    Disentangling the Roles of Functional Domains in the Aggregation and Adsorption of the Multimodular Sea Star Adhesive Protein Sfp12021Ingår i: Marine Biotechnology, ISSN 1436-2228, E-ISSN 1436-2236, Vol. 23, nr 5, s. 724-735Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Sea stars can adhere to various underwater substrata using an adhesive secretion of which Sfp1 is a major component. Sfp1 is a multimodular protein composed of four subunits (Sfp1 Alpha, Beta, Delta, and Gamma) displaying different functional domains. We recombinantly produced two fragments of Sfp1 comprising most of its functional domains: the C-terminal part of the Beta subunit (rSfp1 Beta C-term) and the Delta subunit (rSfp1 Delta). Surface plasmon resonance analyses of protein adsorption onto different model surfaces showed that rSfp1 Beta C-term exhibits a significantly higher adsorption than the fibrinogen control on hydrophobic, hydrophilic protein-resistant, and charged self-assembled monolayers, while rSfp1 Delta adsorbed more on negatively charged and on protein-resistant surfaces compared to fibrinogen. Truncated recombinant rSfp1 Beta C-term proteins were produced in order to investigate the role of the different functional domains in the adsorption of this protein. The analysis of their adsorption capacities on glass showed that two mechanisms are involved in rSfp1 Beta C-term adsorption: (1) one mediated by the EGF-like domain and involving Ca2+ and Mg2+ ions, and (2) one mediated by the sequence of Sfp1 Beta with no homology with known functional domain in databases, in the presence of Na+, Ca2+ and Mg2+ ions.

  • 38.
    Mandenius, Carl-Fredrik
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Measurement Technologies for Upstream and Downstream Bioprocessing2021Ingår i: Processes, ISSN 2227-9717, Vol. 9, nr 1, artikel-id 143Artikel i tidskrift (Övrigt vetenskapligt)
    Abstract [en]

    n/a

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  • 39.
    Mandenius, Carl-Fredrik
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Realization of user-friendly bioanalytical tools to quantify and monitor critical components in bio-industrial processes through conceptual design2022Ingår i: Engineering in Life Sciences, ISSN 1618-0240, E-ISSN 1618-2863, Vol. 22, nr 3-4, s. 217-228Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    This minireview suggests a conceptual and user-oriented approach for the design of process monitoring systems in bioprocessing. Advancement of process analytical techniques for quantification of critical analytes can take advantage of basic conceptual process design to support reasoning, reconsidering and ranking solutions. Issues on analysis in complex bio-industrial media, sensitivity and selectivity are highlighted from users perspectives. Meeting challenging analytical demands for understanding the critical interplay between the emerging bioprocesses, their biomolecular complexity and the needs for user-friendly analytical tools are discussed. By that, a thorough design approach is suggested based on a holistic design thinking in the quest for better analytical opportunities to solve established and emerging analytical needs.

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  • 40.
    Matthiesen, Isabelle
    et al.
    KTH Royal Inst Technol, Sweden; AstraZeneca, Sweden.
    Jury, Michael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rasti Boroojeni, Fatemeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Ludwig, Saskia L.
    KTH Royal Inst Technol, Sweden.
    Holzreuter, Muriel
    Karolinska Inst, Sweden.
    Buchmann, Sebastian
    KTH Royal Inst Technol, Sweden; Karolinska Inst, Sweden; KTH Royal Inst Technol, Sweden.
    Träger, Andrea
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Winkler, Thomas E.
    KTH Royal Inst Technol, Sweden; Tech Univ Carolo Wilhelmina Braunschweig, Germany; Tech Univ Carolo Wilhelmina Braunschweig, Germany.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Herland, Anna
    KTH Royal Inst Technol, Sweden; Karolinska Inst, Sweden; KTH Royal Inst Technol, Sweden.
    Astrocyte 3D culture and bioprinting using peptide functionalized hyaluronan hydrogels2023Ingår i: Science and Technology of Advanced Materials, ISSN 1468-6996, E-ISSN 1878-5514, Vol. 24, nr 1, artikel-id 2165871Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Astrocytes play an important role in the central nervous system, contributing to the development of and maintenance of synapses, recycling of neurotransmitters, and the integrity and function of the blood-brain barrier. Astrocytes are also linked to the pathophysiology of various neurodegenerative diseases. Astrocyte function and organization are tightly regulated by interactions mediated by the extracellular matrix (ECM). Engineered hydrogels can mimic key aspects of the ECM and can allow for systematic studies of ECM-related factors that govern astrocyte behaviour. In this study, we explore the interactions between neuroblastoma (SH-SY5Y) and glioblastoma (U87) cell lines and human fetal primary astrocytes (FPA) with a modular hyaluronan-based hydrogel system. Morphological analysis reveals that FPA have a higher degree of interactions with the hyaluronan-based gels compared to the cell lines. This interaction is enhanced by conjugation of cell-adhesion peptides (cRGD and IKVAV) to the hyaluronan backbone. These effects are retained and pronounced in 3D bioprinted structures. Bioprinted FPA using cRGD functionalized hyaluronan show extensive and defined protrusions and multiple connections between neighboring cells. Possibilities to tailor and optimize astrocyte-compatible ECM-mimicking hydrogels that can be processed by means of additive biofabrication can facilitate the development of advanced tissue and disease models of the central nervous system.

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  • 41.
    Metson, Genevieve
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk Biologi. Linköpings universitet, Tekniska fakulteten.
    Feiz Aghaei, Roozbeh
    Linköpings universitet, Institutionen för ekonomisk och industriell utveckling, Industriell miljöteknik. Linköpings universitet, Tekniska fakulteten.
    Lindegaard, Ida
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Ranggård, Tove
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Quttineh, Nils-Hassan
    Linköpings universitet, Matematiska institutionen, Tillämpad matematik. Linköpings universitet, Tekniska fakulteten.
    Gunnarsson, Emma
    Gasum AB, Linkoping, Sweden.
    Not all sites are created equal - Exploring the impact of constraints to suitable biogas plant locations in Sweden2022Ingår i: Journal of Cleaner Production, ISSN 0959-6526, E-ISSN 1879-1786, Vol. 349, artikel-id 131390Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Biogas production from manure is attractive to support plans towards a circular economy as it allows for renewable energy production and nutrient recycling in agriculture. Finding optimal locations for biogas plants, which minimize transport distances to and from farms, while accounting for multiple feasibility constraints, remains a challenge. We developed 1 km2 spatially-explicit datasets for known feasibility constraints such as distance to housing, compatible land-use zoning, and the presence of roads with sufficient weight bearing capacity. These datasets were used to improve the realism of an optimization model designed to minimize transportation costs in Sweden. At a national level, the presence of durable enough roads most limited the number of suitable locations for a plant. We further focused our analysis on a case study region where a company wanted to invest in a new manure-based biogas plant. In contrast to the national level, the constraint for remaining at least 500 m from housing/buildings had the greatest limiting impact, excluding 71% of grids in the Sjo center dot bo or Tomelilla municipalities of Southern Sweden. Still, we identified 105 suitable locations for a new biogas plant. The most suitable location, accounting for feasibility and minimized transportation costs, changed when simultaneously accounting for another proposed plant in a neighboring municipality. Our results indicate that utilizing both local and national datasets can help narrow down potential biogas development sites and that long-term planning is necessary for actors with ambitions to build several plants to minimize costs and maximize energy and nutrient recycling benefits.

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  • 42.
    Musa, Amani
    et al.
    Orebro Univ, Sweden.
    Wiman, Emanuel
    Orebro Univ, Sweden.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Bengtsson, Torbjörn
    Orebro Univ, Sweden.
    Khalaf, Hazem
    Orebro Univ, Sweden.
    Plantaricin NC8 alpha beta prevents Staphylococcus aureus-mediated cytotoxicity and inflammatory responses of human keratinocytes2021Ingår i: Scientific Reports, E-ISSN 2045-2322, Vol. 11, nr 1, artikel-id 12514Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Multidrug resistance bacteria constitue an increasing global health problem and the development of novel therapeutic strategies to face this challenge is urgent. Antimicrobial peptides have been proven as potent agents against pathogenic bacteria shown by promising in vitro results. The aim of this study was to characterize the antimicrobial effects of PLNC8 alpha beta on cell signaling pathways and inflammatory responses of human keratinocytes infected with S. aureus. PLNC8 alpha beta did not affect the viability of human keratinocytes but upregulated several cytokines (IL-1 beta, IL-6, CXCL8), MMPs (MMP1, MMP2, MMP9, MMP10) and growth factors (VEGF and PDGF-AA), which are essential in cell regeneration. S. aureus induced the expression of several inflammatory mediators at the gene and protein level and PLNC8 alpha beta was able to significantly suppress these effects. Intracellular signaling events involved primarily c-Jun via JNK, c-Fos and NF kappa B, suggesting their essential role in the initiation of inflammatory responses in human keratinocytes. PLNC8 alpha beta was shown to modulate early keratinocyte responses, without affecting their viability. The peptides have high selectivity towards S. aureus and were efficient at eliminating the bacteria and counteracting their inflammatory and cytotoxic effects, alone and in combination with low concentrations of gentamicin. We propose that PLNC8 alpha beta may be developed to combat infections caused by Staphylococcus spp.

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  • 43. Beställ onlineKöp publikationen >>
    Naeimipour, Sajjad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Modular Enzyme-Responsive Polysaccharide-Based Hydrogels for Biofabrication2023Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
    Abstract [en]

    Engineered human tissue and disease models can decrease the cost and time of developing new drugs and treatments, facilitate personalized medicine, and eliminate the need for animal models that poorly represent the human body and are ethically problematic. However, the current conventional cell expansion methods using 2D culture flasks cannot enable the development of such complex multi-cellular 3D models. In general, hydrogels are considered promising materials that can make the biofabrication of tissue models possible. Hydrogels are highly hydrated materials comprised of either synthetic or naturally derived polymers, or a combination of both, and can form an environment mimicking the biomacromolecular network surrounding cells in the body. This network of biopolymers, known as extracellular matrix (ECM), is comprised of proteins such as collagen, laminin, fibronectin, and polysaccharides such as hyaluronan (HA), heparan, keratan, and chondroitin sulfate. The design of hydrogels representing the physical and biochemical properties of the ECM and which can be used for biofabrication is challenging but of increasing interest due to the rapid progress in the development of 3D and 4D bioprinting techniques. As the ECM properties differ between various tissues and disease conditions and change over time, a dynamic modular hydrogel system is needed to that can be optimized for each cell and tissue type. This thesis aims to develop modular enzyme-responsive polysaccharide-based hydrogels for 3D cell culture and biofabrication. The natural polysaccharides, hyaluronic acid (HA) and alginate (Alg) were used as the main backbone in the hydrogels developed in this thesis. HA was modified by conjugating bicyclo[6.1.0]non-4-yne (BCN) to the backbone to form HA-BCN-based hydrogels by a bioorthogonal strain-promoted alkyne-azide cycloaddition. The click reaction between BCN and azide groups allowed for modulating the biochemical and mechanical properties of the HA-BCN hydrogels. HA-BCN was further decorated with peptides to explore peptide folding and dimerization-mediated dynamic cross-linking and biofunctionalization. This system was further used to explore possibilities to dynamically alter the properties of 3D bioprinted structures, mimicking the biomineralization process in bone tissue. In a different study, a tumor model comprising fibroblast and breast cancer cells (MCF7) was bioprinted using HA-BCN cross-linked by matrix metalloporotease (MMP) cleavable and PEG-diazide MMP-resistant cross-linkers, demonstrating the synergistic relationship between hydrogel degradability and cancer cell growth, intensified by the presence of fibroblasts. The possibility of incorporating a conductive module into this hydrogel system was explored using the enzyme-assisted polymerization of ETE-S to form an interpenetrating conductive network inside HA-BCN hydrogel. The in situ and user-triggered polymerization of conductive ETE-S was demonstrated after 3D printing HA-BCN bioink containing ETE-S monomers into a lattice shape structure. We also demonstrated that cellulose nanofibrils (CNF) improved the printability of HA-BCN bioinks, and this hybrid bioink was used for printing self-standing cell-laden 3D structures. Besides these studies, a novel enzymatically triggered thiol-based chemistry was developed to address the unwanted oxidation of thiol-containing hydrogels and decrease the off-target thiol reactions during hydrogel synthesis and formation. Alginate containing sulfhydryl moieties, protected by an enzyme-labile Phacm group (AlgCP), was treated with penicillin G acylase and subsequently formed a disulfide cross-linked hydrogel. We studied the gelation kinetics and rheological properties of AlgCP and different modes of cross-linking by reversible disulfide bonds, a thiol-maleimide Micheale-type addition reaction, and ionic interactions between alginate and Ca2+ ions. MCF7 breast cancer cells cultured in the AlgCP hydrogels formed spheroids that could be harvested by GSH dissolution of the hydrogels. Finally, this novel chemistry enabled bioprinting of multi-material 3D structures with control over the printed structure's physiochemical properties, including the type and density of cross-linkers. Bioprinted fibroblasts formed extended morphology, and MCF7 cells formed spheroids in the bioprinted lattice structures.   

    The hydrogel systems developed and explored in this thesis are modular and exhibit dynamic and tunable properties, and are applicable for a wide range of 3D cell culture and bioprinting applications. The hydrogels were either formed in response to the activity of an enzyme or remodeled by enzymes. Both enzyme-responsive HA-BCN and AlgCP hydrogel systems are promising bioinks for generating more elaborate and spatially defined cell-laden 3D structures whose features can be altered post-printing by cell-secreted and extrinsic reagents. These hydrogel-based toolkits can play a vital role in developing tissue and disease models that can make the drug discovery process faster, cheaper, and animal-free. 

    Delarbeten
    1. Dynamic peptide-folding mediated biofunctionalization and modulation of hydrogels for 4D bioprinting
    Öppna denna publikation i ny flik eller fönster >>Dynamic peptide-folding mediated biofunctionalization and modulation of hydrogels for 4D bioprinting
    Visa övriga...
    2020 (Engelska)Ingår i: Biofabrication, ISSN 1758-5082, E-ISSN 1758-5090, Vol. 12, nr 3, artikel-id 035031Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Hydrogels are used in a wide range of biomedical applications, including three-dimensional (3D) cell culture, cell therapy and bioprinting. To enable processing using advanced additive fabrication techniques and to mimic the dynamic nature of the extracellular matrix (ECM), the properties of the hydrogels must be possible to tailor and change over time with high precision. The design of hydrogels that are both structurally and functionally dynamic, while providing necessary mechanical support is challenging using conventional synthesis techniques. Here, we show a modular and 3D printable hydrogel system that combines a robust but tunable covalent bioorthogonal cross-linking strategy with specific peptide-folding mediated interactions for dynamic modulation of cross-linking and functionalization. The hyaluronan-based hydrogels were covalently cross-linked by strain-promoted alkyne-azide cycloaddition using multi-arm poly(ethylene glycol). In addition, ade novodesigned helix-loop-helix peptide was conjugated to the hyaluronan backbone to enable specific peptide-folding modulation of cross-linking density and kinetics, and hydrogel functionality. An array of complementary peptides with different functionalities was developed and used as a toolbox for supramolecular tuning of cell-hydrogel interactions and for controlling enzyme-mediated biomineralization processes. The modular peptide system enabled dynamic modifications of the properties of 3D printed structures, demonstrating a novel route for design of more sophisticated bioinks for four-dimensional bioprinting.

    Ort, förlag, år, upplaga, sidor
    IOP PUBLISHING LTD, 2020
    Nyckelord
    hydrogel; hyaluronan; peptide; folding; bioprinting; biomineralization
    Nationell ämneskategori
    Cell- och molekylärbiologi
    Identifikatorer
    urn:nbn:se:liu:diva-168253 (URN)10.1088/1758-5090/ab9490 (DOI)000548339700001 ()32428894 (PubMedID)
    Anmärkning

    Funding Agencies|Swedish Foundation for Strategic Research (SFF)Swedish Foundation for Strategic Research [FFL15-0026]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Carl Tryggers Foundation [CTS15:7, CTS18:5]; Knut and Alice Wallenberg FoundationKnut & Alice Wallenberg Foundation [KAW 2016.0231]

    Tillgänglig från: 2020-08-22 Skapad: 2020-08-22 Senast uppdaterad: 2024-02-07
    2. Enzymatically Triggered Deprotection and Cross-Linking of Thiolated Alginate-Based Bioinks
    Öppna denna publikation i ny flik eller fönster >>Enzymatically Triggered Deprotection and Cross-Linking of Thiolated Alginate-Based Bioinks
    2022 (Engelska)Ingår i: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 34, nr 21, s. 9536-9545Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Thiolated polymers are widely used in hydrogels for drug delivery, tissue engineering, and biofabrication. The oxidation of thiols is spontaneous, resulting in the formation of disulfide bridges and cross linking of polymers. The cross-linking process is, however, difficult to control and is initiated directly when the thiolated components are exposed to ambient conditions, which significantly complicates handling of the materials. Here, we show a fully bioorthogonal enzyme-mediated thiol-based chemistry for dynamic covalent cross-linking of carbohydrate-based hydrogels that circumvents the problems with uncontrolled thiol oxidation. Alginate was modified with cysteine residues, protected by an enzyme-labile thiol-protecting group (Phacm). Releasing the Phacm group by penicillin G acylase generates free thiols that oxidize under physiological conditions, resulting in a reversible cross-linking and formation of hydrogels with tunable stiffness. Prior to deprotection, the components can be exposed to ambient conditions. The enzyme-triggered deprotection and subsequent gelation allows for encapsulation of cells and 3D bioprinting of cell-laden hydrogel structures. Remaining deprotected thiols enabled postprinting modifications and hydrogel self-healing. The proposed hydrogel synthesis strategy significantly increases the versatility of thiol-based cross-linking chemistries and provides new possibilities to generate dynamic covalent hydrogels for a broad range of biomedical applications.

    Ort, förlag, år, upplaga, sidor
    American Chemical Society (ACS), 2022
    Nationell ämneskategori
    Polymerkemi
    Identifikatorer
    urn:nbn:se:liu:diva-189941 (URN)10.1021/acs.chemmater.2c02037 (DOI)000877338100001 ()
    Anmärkning

    Funding Agencies|Swedish Foundation for Strategic Research (SFF) [FFL15-0026]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009-00971]; Carl Tryggers Foundation; Knut and Alice Wallenberg Foundation [KAW 2016.0231, 2021.0186]

    Tillgänglig från: 2022-11-15 Skapad: 2022-11-15 Senast uppdaterad: 2024-01-10Bibliografiskt granskad
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  • 44.
    Naeimipour, Sajjad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rasti Boroojeni, Fatemeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Lifwergren, Philip
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Multimodal and dynamic cross-linking of modular thiolated alginate-based bioinks2023Ingår i: Materials Today Advances, E-ISSN 2590-0498, Vol. 19, artikel-id 100415Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Engineered extracellular matrix-mimicking hydrogels can facilitate 3D cell culture and fabrication of tissue-like constructs and biologically relevant disease models. Processing of cell-laden hydrogels using additive manufacturing techniques further allows for the development of tissue-mimetic structures with higher spatial complexity. Whereas a wide range of printable hydrogels is available, they tend to lack biological functionality and cell compatibility. Here we show an enzymatically mediated thiol-based cross-linking strategy for the design of modular and cytocompatible hydrogel-based bioinks for 3D bioprinting of dynamic multi-material architectures. Alginate is functionalized with cysteines modified with an enzyme-labile thiol protection group. Deprotection using penicillin G acylase (PGA) generates free thiols on-demand, enabling hydrogel cross-linking using thiol-reactive cross-linkers and intermolecular disulfides while avoiding undesired and uncontrolled thiol oxidation. Remaining free thiols can be used for post-printing hydrogel functionalization and lamination of multilayer structures. Moreover, the addition of PGA to a thermo-reversible hydrogel support bath enables the bioprinting of cell-laden 3D structures with high cell viability and excellent shape fidelity. The possibilities to enzymatically generate free thiols during bioprinting facilitate cross-linking and tuning of bioink properties using cytocompatible chemistries and allow for the printing of complex and dynamic cell-laden structures.

  • 45.
    Naeimipour, Sajjad
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Rasti Boroojeni, Fatemeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Enzymatically Triggered Deprotection and Cross-Linking of Thiolated Alginate-Based Bioinks2022Ingår i: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 34, nr 21, s. 9536-9545Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Thiolated polymers are widely used in hydrogels for drug delivery, tissue engineering, and biofabrication. The oxidation of thiols is spontaneous, resulting in the formation of disulfide bridges and cross linking of polymers. The cross-linking process is, however, difficult to control and is initiated directly when the thiolated components are exposed to ambient conditions, which significantly complicates handling of the materials. Here, we show a fully bioorthogonal enzyme-mediated thiol-based chemistry for dynamic covalent cross-linking of carbohydrate-based hydrogels that circumvents the problems with uncontrolled thiol oxidation. Alginate was modified with cysteine residues, protected by an enzyme-labile thiol-protecting group (Phacm). Releasing the Phacm group by penicillin G acylase generates free thiols that oxidize under physiological conditions, resulting in a reversible cross-linking and formation of hydrogels with tunable stiffness. Prior to deprotection, the components can be exposed to ambient conditions. The enzyme-triggered deprotection and subsequent gelation allows for encapsulation of cells and 3D bioprinting of cell-laden hydrogel structures. Remaining deprotected thiols enabled postprinting modifications and hydrogel self-healing. The proposed hydrogel synthesis strategy significantly increases the versatility of thiol-based cross-linking chemistries and provides new possibilities to generate dynamic covalent hydrogels for a broad range of biomedical applications.

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  • 46. Beställ onlineKöp publikationen >>
    Nagy, Bela
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Neutron Reflectometry Studies of the Hydrated Structure of Polymer Thin Films2022Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
    Abstract [en]

    Polymer coatings are inexpensive surface modifications providing a wide variety of functions. There is an ever-present motivation to improve the films’ performance and to decrease the cost and the environmental footprint of their production. This thesis includes the study of the structural and functional parameters of polymer coatings that are aimed at preventing biological fouling, the unwanted attachment of organic molecules and organisms on surfaces. The focus was on thin films prepared by the self-initiated photografting and photopolymerization method. This is a UV-initiated polymerization reaction that does not require additional chemicals beyond the monomers and the solvent. Since biofouling is a prominent problem in wet environments, the emphasis was placed on the hydrated structure of the films. Neutron reflectometry was selected as a primary method for these studies, since it is a powerful method for investigating the structure of polymer thin films, especially in the hydrated state due to the labelling offered by isotope substitution. This allows the determination of the solvent volume fraction depth profile, which reveals the chain segment density profile in the hydrated film. To resolve fast changes in the film structure and to study the chemical composition, spectroscopic ellipsometry and infrared absorption spectroscopy was implemented in a setup for in-situ measurements in parallel with neutron reflectometry.  

    This thesis contains an introduction and five research articles, and it can be divided into two main parts: the first focusing on the polymerization reaction and the resulting polymer films and the second on the reflectivity method and instrumentation development. Firstly, uncharged hydrophilic polymer layers were prepared by self-initiated photografting and photopolymerization and the hydrated structure of these was investigated. It was found that the films follow a stretched profile indicating negligible crosslinking, and that the growth dynamics is determined by the balance of grafting and removal through radiation damage. Studying sequential grafting of oppositely charged polyelectrolytes confirmed the results on growth dynamics and showed the effects of electrostatic interactions between the monomers. This also demonstrated that the polymerization method is ill suited for preparing block co-polymers due to the removal of material from the previous layer. However, these studies also show that the growth of the second layer tends to proceed from the substrate, forming a system where the two kinds of chains co-exist and interact in the same layer. The grafting of random co-polymers was also investigated by comparing the anti-fouling performance of layers made from a mixture of oppositely charged monomers to layers made using zwitterionic polymers, resulting in no significant difference. This was attributed to the pairwise deposition of oppositely charged monomers, further emphasizing the importance of the Coulomb force in defining the structure of the charged films. The second part of this work focuses on instrument development. Here the building and testing of an angle-dispersive reflectometer is presented, and the design and first applications of an in-situ setup for measuring spectroscopic ellipsometry and infrared spectroscopy along with neutron reflectometry is described. 

    By investigating the structure of the polymer films prepared by self-initiated photografting and photopolymerization, this work improved the understanding of this method, facilitating the development of new applications in the future. By combining additional methods with neutron reflectometry, both fast changes in the structure and the chemical evolution of the samples can be investigated. However, the differences in the sensitivities and the structural models required by the probes present new challenges in modelling. 

    Delarbeten
    1. Structure and pH-Induced Swelling of Polymer Films Prepared from Sequentially Grafted Polyelectrolytes
    Öppna denna publikation i ny flik eller fönster >>Structure and pH-Induced Swelling of Polymer Films Prepared from Sequentially Grafted Polyelectrolytes
    2022 (Engelska)Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 38, nr 5, s. 1725-1737Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    We have prepared a series of ampholytic polymer films, using a self-initiated photografting and photopolymerization (SI-PGP) method to sequentially polymerize first anionic (deuterated methacrylic acid (dMAA)) and thereafter cationic (2-aminoethyl methacrylate (AEMA)) monomers to investigate the SI-PGP grafting process. Dry films were investigated by ellipsometry, X-ray, and neutron reflectometry, and their swelling was followed over a pH range from 4.5 to 10.5 with spectroscopic ellipsometry. The deuterated monomer allows us to separate the distributions of the two components by neutron reflectometry. Growth of both polymers proceeds via grafting of solution-polymerized fragments to the surface, and also the second layer is primarily grafted to the substrate and not as a continuation of the existing chains. The polymer films are stratified, with one layer of near 1:1 composition and the other layer enriched in one component and located either above or below the former layer. The ellipsometry results show swelling transitions at low and high pH but with no systematic variation in the pH values where these transitions occur. The results suggest that grafting density in SI-PGP-prepared homopolymers could be increased via repeated polymerization steps, but that this process does not necessarily increase the average chain length.

    Ort, förlag, år, upplaga, sidor
    American Chemical Society (ACS), 2022
    Nationell ämneskategori
    Polymerkemi
    Identifikatorer
    urn:nbn:se:liu:diva-183922 (URN)10.1021/acs.langmuir.1c02784 (DOI)000763586100009 ()35081310 (PubMedID)
    Anmärkning

    Funding Agencies|Swedish Research Council (Vetenskapsradet)Swedish Research Council [2014-4004]; Swedish Research Council (Rontgen-Angstrom grant, Vetenskapsradet) [2017-06696]; German Research Foundation (Deutsche Forschungsgemeinschaft, DFG)German Research Foundation (DFG) [107745057-TRR80]

    Tillgänglig från: 2022-04-01 Skapad: 2022-04-01 Senast uppdaterad: 2023-12-28
    2. Structure of Self-Initiated Photopolymerized Films: A Comparison of Models
    Öppna denna publikation i ny flik eller fönster >>Structure of Self-Initiated Photopolymerized Films: A Comparison of Models
    2022 (Engelska)Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 38, nr 45, s. 14004-14015Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Self-initiated photografting and photopolymerization (SI-PGP) uses UV illumination to graft polymers to surfaces without additional photoinitiators using the monomers as initiators, “inimers”. A wider use of this method is obstructed by a lack of understanding of the resulting, presumably heterogeneous, polymer structure and of the parallel degradation under continuous UV illumination. We have used neutron reflectometry to investigate the structure of hydrated SI-PGP-prepared poly(HEMA-co-PEG10MA) (poly(2-hydroxyethyl methacrylate-co-(ethylene glycol)10 methacrylate)) films and compared parabolic, sigmoidal, and Gaussian models for the polymer volume fraction distributions. Results from fitting these models to the data suggest that either model can be used to approximate the volume fraction profile to similar accuracy. In addition, a second layer of deuterated poly(methacrylic acid) (poly(dMAA)) was grafted over the existing poly(HEMA-co-PEG10MA) layer, and the resulting double-grafted films were also studied by neutron reflectometry to shed light on the UV-polymerization process and the inevitable UV-induced degradation which competes with the grafting.

    Ort, förlag, år, upplaga, sidor
    American Chemical Society, 2022
    Nationell ämneskategori
    Polymerkemi
    Identifikatorer
    urn:nbn:se:liu:diva-190018 (URN)10.1021/acs.langmuir.2c02396 (DOI)000881133700001 ()
    Forskningsfinansiär
    Vetenskapsrådet, 2014-04004; 2017-06696
    Tillgänglig från: 2022-11-17 Skapad: 2022-11-17 Senast uppdaterad: 2023-12-28Bibliografiskt granskad
    3. Polyampholytic Poly(AEMA-co-SPMA) Thin Films and Their Potential for Antifouling Applications
    Öppna denna publikation i ny flik eller fönster >>Polyampholytic Poly(AEMA-co-SPMA) Thin Films and Their Potential for Antifouling Applications
    Visa övriga...
    2021 (Engelska)Ingår i: ACS Applied Polymer Materials, ISSN 2637-6105, Vol. 3, nr 11, s. 5361-5372Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Polyampholytic poly(2-aminoethyl methacrylate-co-sulfopropyl methacrylate) (p(AEMA-co-SPMA)) thin films were prepared by self-initiated photopolymerization and photografting (SIPGP) and are demonstrated to be a potential alternative to films prepared from zwitterionic poly(sulfobetaine methacrylate) (pSBMA) for antifouling applications. SIPGP allows polymerization from aqueous solutions containing only monomers, implying that p(AEMA-co-SPMA) thin films can be prepared simply and inexpensively without the risk of introducing potentially toxic substances necessary in many controlled polymerization reactions. For the polymers, wettabilities were studied by contact angle goniometry, the compositions of the films were determined by infrared and X-ray photoelectron spectroscopies, and streaming current measurements were used to assess their net charge. The antibiofouling properties were compared via adsorption of fibrinogen and bovine serum albumin, settlement of algal zoospores, and the growth of sporelings of the marine alga Ulva lactuca. The fouling of the p(AEMA-co-SPMA) copolymer was in several respects similar to that of the zwitterionic pSBMA and suggests that it is potentially suitable for applications under high-salinity conditions, such as marine or physiological environments.

    Ort, förlag, år, upplaga, sidor
    American Chemical Society (ACS), 2021
    Nyckelord
    self-initiated photopolymerization and photografting; polyampholyte; poly(AEMA-co-SPMA); protein adsorption; marine biofouling; spore settlement; Ulva lactuca
    Nationell ämneskategori
    Polymerkemi
    Identifikatorer
    urn:nbn:se:liu:diva-181682 (URN)10.1021/acsapm.1c00383 (DOI)000719860800004 ()
    Anmärkning

    Funding Agencies|European Communitys Seventh Framework Program FP7/2007-2013 [237997]; Swedish Research Council (VR)Swedish Research Council [2014-04004, 2017-06696, 621-2013-5357]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Carl Tryggers Stiftelse [CTS 15:507]

    Tillgänglig från: 2021-12-07 Skapad: 2021-12-07 Senast uppdaterad: 2023-12-28
    4. A mobile setup for simultaneous and in situ neutron reflectivity, infrared spectroscopy, and ellipsometry studies
    Öppna denna publikation i ny flik eller fönster >>A mobile setup for simultaneous and in situ neutron reflectivity, infrared spectroscopy, and ellipsometry studies
    Visa övriga...
    2022 (Engelska)Ingår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 93, nr 11Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Neutron reflectivity at the solid/liquid interface offers unique opportunities for resolving the structure–function relationships of interfacial layers in soft matter science. It is a non-destructive technique for detailed analysis of layered structures on molecular length scales, providing thickness, density, roughness, and composition of individual layers or components of adsorbed films. However, there are also some well-known limitations of this method, such as the lack of chemical information, the difficulties in determining large layer thicknesses, and the limited time resolution. We have addressed these shortcomings by designing and implementing a portable sample environment for in situ characterization at neutron reflectometry beamlines, integrating infrared spectroscopy under attenuated total reflection for determination of molecular entities and their conformation, and spectroscopic ellipsometry for rapid and independent measurement of layer thicknesses and refractive indices. The utility of this combined setup is demonstrated by two projects investigating (a) pH-dependent swelling of polyelectrolyte layers and (b) the impact of nanoparticles on lipid membranes to identify potential mechanisms of nanotoxicity. 

    Ort, förlag, år, upplaga, sidor
    American Institute of Physics, 2022
    Nationell ämneskategori
    Fysikalisk kemi
    Identifikatorer
    urn:nbn:se:liu:diva-190021 (URN)10.1063/5.0118329 (DOI)000936778000014 ()36461462 (PubMedID)
    Anmärkning

    Funding agencies: Rontgen-Angstrom grant (Vetenskapsradet) [VR 2017-06696]; Rontgen-Angstrom grant (BMBF) [05K18VHA]; Swedish Research Council (Vetenskapsradet) [2014-4004]

    Tillgänglig från: 2022-11-17 Skapad: 2022-11-17 Senast uppdaterad: 2023-12-28Bibliografiskt granskad
    5. GINA—A polarized neutron reflectometer at the Budapest Neutron Centre
    Öppna denna publikation i ny flik eller fönster >>GINA—A polarized neutron reflectometer at the Budapest Neutron Centre
    Visa övriga...
    2013 (Engelska)Ingår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 84, nr 1Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    The setup, capabilities, and operation parameters of the neutron reflectometer GINA, the recently installed “Grazing Incidence Neutron Apparatus” at the Budapest Neutron Centre, are introduced. GINA, a dance-floor-type, constant-energy, angle-dispersive reflectometer is equipped with a 2D position-sensitive detector to study specular and off-specular scattering. Wavelength options between 3.2 and 5.7 Å are available for unpolarized and polarized neutrons. Spin polarization and analysis are achieved by magnetized transmission supermirrors and radio-frequency adiabatic spin flippers. As a result of vertical focusing by a five-element pyrolytic graphite monochromator, the reflected intensity from a 20 × 20 mm2 sample has been doubled. GINA is dedicated to studies of magnetic films and heterostructures, but unpolarized options for non-magnetic films, membranes, and other surfaces are also provided. Shortly after its startup, reflectivity values as low as 3 × 10−5 have been measured by the instrument. The instrument capabilities are demonstrated by a non-polarized and a polarized reflectivity experiment on a Si wafer and on a magnetic film of [62Ni/natNi]5 isotope-periodic layer composition. The facility is now open for the international user community. Its further development is underway establishing new sample environment options and spin analysis of off-specularly scattered radiation as well as further decreasing the background.

    Ort, förlag, år, upplaga, sidor
    American Institute of Physics, 2013
    Nationell ämneskategori
    Acceleratorfysik och instrumentering
    Identifikatorer
    urn:nbn:se:liu:diva-189396 (URN)10.1063/1.4770129 (DOI)
    Anmärkning

    Funding agencies: This work was partially supported by the National Office for Research and Technology of Hungary and the Hungarian National Science Fund (OTKA) under contracts NAP-VENEUS'05 and K 62272, respectively. Mobility support for A. V. Petrenko by the bilateral project between JINR (Dubna) and the Hungarian Academy of Sciences is gratefully appreciated.

    Tillgänglig från: 2022-10-19 Skapad: 2022-10-19 Senast uppdaterad: 2023-12-28Bibliografiskt granskad
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  • 47.
    Nagy, Bela
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Campana, Mario
    STFC, England.
    Khaydukov, Yury N.
    Max Planck Inst Festkorpetforsch, Germany; Heinz Maier Leibnitz Zentrum MLZ, Germany.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Structure and pH-Induced Swelling of Polymer Films Prepared from Sequentially Grafted Polyelectrolytes2022Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 38, nr 5, s. 1725-1737Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    We have prepared a series of ampholytic polymer films, using a self-initiated photografting and photopolymerization (SI-PGP) method to sequentially polymerize first anionic (deuterated methacrylic acid (dMAA)) and thereafter cationic (2-aminoethyl methacrylate (AEMA)) monomers to investigate the SI-PGP grafting process. Dry films were investigated by ellipsometry, X-ray, and neutron reflectometry, and their swelling was followed over a pH range from 4.5 to 10.5 with spectroscopic ellipsometry. The deuterated monomer allows us to separate the distributions of the two components by neutron reflectometry. Growth of both polymers proceeds via grafting of solution-polymerized fragments to the surface, and also the second layer is primarily grafted to the substrate and not as a continuation of the existing chains. The polymer films are stratified, with one layer of near 1:1 composition and the other layer enriched in one component and located either above or below the former layer. The ellipsometry results show swelling transitions at low and high pH but with no systematic variation in the pH values where these transitions occur. The results suggest that grafting density in SI-PGP-prepared homopolymers could be increased via repeated polymerization steps, but that this process does not necessarily increase the average chain length.

    Ladda ner fulltext (pdf)
    fulltext
  • 48.
    Nagy, Bela
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Ekblad, Tobias
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Fragneto, Giovanna
    Institut Laue-Langevin, Grenoble, France.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Structure of Self-Initiated Photopolymerized Films: A Comparison of Models2022Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 38, nr 45, s. 14004-14015Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Self-initiated photografting and photopolymerization (SI-PGP) uses UV illumination to graft polymers to surfaces without additional photoinitiators using the monomers as initiators, “inimers”. A wider use of this method is obstructed by a lack of understanding of the resulting, presumably heterogeneous, polymer structure and of the parallel degradation under continuous UV illumination. We have used neutron reflectometry to investigate the structure of hydrated SI-PGP-prepared poly(HEMA-co-PEG10MA) (poly(2-hydroxyethyl methacrylate-co-(ethylene glycol)10 methacrylate)) films and compared parabolic, sigmoidal, and Gaussian models for the polymer volume fraction distributions. Results from fitting these models to the data suggest that either model can be used to approximate the volume fraction profile to similar accuracy. In addition, a second layer of deuterated poly(methacrylic acid) (poly(dMAA)) was grafted over the existing poly(HEMA-co-PEG10MA) layer, and the resulting double-grafted films were also studied by neutron reflectometry to shed light on the UV-polymerization process and the inevitable UV-induced degradation which competes with the grafting.

    Ladda ner fulltext (pdf)
    fulltext
  • 49.
    Nilsson, Martin
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik.
    GIANT UNILAMELLAR VESICLES FOR PEPTIDE-MEMBRANE INTERACTION STUDIES USING FLUORESCENCE MICROSCOPY2020Självständigt arbete på avancerad nivå (masterexamen), 20 poäng / 30 hpStudentuppsats (Examensarbete)
    Abstract [en]

    Vesicles are a type of biological or biomimetic particle consisting of one or more often spherical bilayers made up of amphipathic molecules, creating a closed system. They can function as an encapsulating device, holding hydrophilic molecules on the inside of the bilayer membrane(s) or hydrophobic molecules in the non-polar interstitial space in the middle of the bilayers. Because of this capacity to carry molecules, vesicles are a premier system for drug delivery and even theranostics in vivo. A peptide-based approach to release of encapsulated molecules has previously been developed but since drug delivery vesicles are in the size range of nanometers, the mechanisms have not been visualized. This project aims to produce giant unilamellar vesicles as a model system used to visualize membrane interactions vital to the understanding and further development of smaller vesicle-based systems for drug delivery. Giant unilamellar vesicles were produced successfully and a preparation protocol was established. Additionally, some membrane interactions were investigated using fluorescence microscopy.

    Ladda ner fulltext (pdf)
    Martin Nilsson master's thesis final draft
  • 50.
    Omer, Abubakr A. M.
    et al.
    Orebro Univ, Sweden.
    Hinkula, Jorma
    Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för molekylär medicin och virologi. Linköpings universitet, Medicinska fakulteten.
    Pham-Tue-Hung, Tran
    Orebro Univ, Sweden.
    Melik, Wessam
    Orebro Univ, Sweden.
    Zattarin, Elisa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Aili, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Selegård, Robert
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biofysik och bioteknik. Linköpings universitet, Tekniska fakulteten.
    Bengtsson, Torbjorn
    Orebro Univ, Sweden.
    Khalaf, Hazem
    Orebro Univ, Sweden.
    Plantaricin NC8 alpha beta rapidly and efficiently inhibits flaviviruses and SARS-CoV-2 by disrupting their envelopes2022Ingår i: PLOS ONE, E-ISSN 1932-6203, Vol. 17, nr 11, artikel-id e0278419Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Potent broad-spectrum antiviral agents are urgently needed to combat existing and emerging viral infections. This is particularly important considering that vaccine development is a costly and time consuming process and that viruses constantly mutate and render the vaccine ineffective. Antimicrobial peptides (AMP), such as bacteriocins, are attractive candidates as antiviral agents against enveloped viruses. One of these bacteriocins is PLNC8 alpha beta, which consists of amphipathic peptides with positive net charges that display high affinity for negatively charged pathogen membrane structures, including phosphatidylserine rich lipid membranes of viral envelopes. Due to the morphological and physiological differences between viral envelopes and host cell plasma membranes, PLNC8 alpha beta is thought to have high safety profile by specifically targeting viral envelopes without effecting host cell membranes. In this study, we have tested the antiviral effects of PLNC8 alpha beta against the flaviviruses Langat and Kunjin, coronavirus SARS-CoV-2, influenza A virus (IAV), and human immunodeficiency virus-1 (HIV-1). The concentration of PLNC8 alpha beta that is required to eliminate all the infective virus particles is in the range of nanomolar (nM) to micromolar (mu M), which is surprisingly efficient considering the high content of cholesterol (8-35%) in their lipid envelopes. We found that viruses replicating in the endoplasmic reticulum (ER)/Golgi complex, e.g. SARS-CoV-2 and flaviviruses, are considerably more susceptible to PLNC8 alpha beta, compared to viruses that acquire their lipid envelope from the plasma membrane, such as IAV and HIV-1. Development of novel broad-spectrum antiviral agents can significantly benefit human health by rapidly and efficiently eliminating infectious virions and thereby limit virus dissemination and spreading between individuals. PLNC8 alpha beta can potentially be developed into an effective and safe antiviral agent that targets the lipid compartments of viral envelopes of extracellular virions, more or less independent of virus antigenic mutations, which faces many antiviral drugs and vaccines.

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