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Regeneration of functional nerves within full thickness collagen-phosphorylcholine corneal substitute implants in guinea pigs
Univ Ottawa, Ottawa Hosp, Inst Eye, Ottawa, ON K1H 8L6 Canada.
Univ Miguel Hernandez, CSIC, Inst Neurociencias Alicante, Alacant 03550, Spain.
Univ Miguel Hernandez, CSIC, Inst Neurociencias Alicante, Alacant 03550, Spain.
Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China.
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2010 (English)In: Biomaterials, ISSN 0142-9612, E-ISSN 1878-5905, Vol. 31, no 10, 2770-2778 p.Article in journal (Refereed) Published
Abstract [en]

Our objective was to evaluate promotion of tissue and nerve regeneration by extracellular matrix (ECM) Mimics, using corneal implantation as a model system. Porcine type I collagen and 2-methacryloyloxyethyl phosphorylcholine (MPC) were crosslinked using 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) and moulded into appropriate corneal dimensions to serve as substitutes for natural corneal ECK These were implanted as full thickness grafts by penetrating keratoplasty into the corneas Of guinea pigs after removal of the host tissue, and tracked over eight months, by clinical examination, slit-lamp biomicroscopy, and esthesiometry. Histopathology and ex vivo nerve terminal impulse recordings were performed at three months and at eight months. The implants promoted regeneration of corneal cells, nerves and the tear film, while retaining optical clarity. After three months, electrophysiological recordings showed evidence of mechano-nociceptors, and polymodal units inside the implants, while cold-sensitive units were present only on the peripheral host cornea. Following eight months, the incidence of nerve activity and the frequency of spontaneous firing were higher than in control eyes as reported for regenerating fibers. Active cold nerve terminals also innervated the implant area. We show that ECM mimetic materials can promote regeneration of corneal cells and functional nerves. The simplicity in fabrication and demonstrated functionality shows potential for ECM substitutes in future clinical applications. (C) 2009 Elsevier Ltd. All rights reserved.

Place, publisher, year, edition, pages
2010. Vol. 31, no 10, 2770-2778 p.
Keyword [en]
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Medical and Health Sciences
URN: urn:nbn:se:liu:diva-65516DOI: 10.1016/j.biomaterials.2009.12.031OAI: diva2:396190
Available from: 2011-02-09 Created: 2011-02-09 Last updated: 2013-12-17

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