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Ericson Jogsten, IngridORCID iD iconorcid.org/0000-0002-6330-789X
Alternative names
Publications (2 of 2) Show all publications
Geng, D., Ericson Jogsten, I., Dunstan, J., Hagberg, J., Wang, T., Ruzzin, J., . . . van Bavel, B. (2016). Gas chromatography/atmospheric pressure chemical ionization/mass spectrometry for the analysis of organochlorine pesticides and polychlorinated biphenyls in human serum. Journal of Chromatography A, 1453, 88-98
Open this publication in new window or tab >>Gas chromatography/atmospheric pressure chemical ionization/mass spectrometry for the analysis of organochlorine pesticides and polychlorinated biphenyls in human serum
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2016 (English)In: Journal of Chromatography A, ISSN 0021-9673, E-ISSN 1873-3778, Vol. 1453, p. 88-98Article in journal (Refereed) Published
Abstract [en]

A method using a novel atmospheric pressure chemical ionization source for coupling gas chromatography (GC/APCI) to triple quadrupole mass spectrometry (MS/MS) for the determination of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) regulated by the Stockholm Convention is presented. One microliter injection of a six-point calibration curve of native PCBs and OCPs, ranging from 0.04 to 300 pg/μL, was performed. The relative standard deviation (RSD) of the relative response factors (RRFs) was less than 15% with a coefficient of determination (r2) >0.995. Meanwhile, two calibration solutions (CS), CS 2 (0.4 pg/μL) and CS 3 (4 pg/μL) were analyzed to study the repeatability calculated for both area and RRFs. The RSD for RRF ranged from 3.1 to 16% and 3.6 to 5.5% for CS 2 and CS 3, respectively. The limits of detection (LOD) determined by peak-to-peak signal-to-noise ratio (S/N) of 3 were compared between the GC/APCI/MS/MS and a GC coupled to high resolution mass spectrometry (GC/HRMS) system. GC/APCI/MS/MS resulted in lower LOD for most of the compounds, except for PCB#74, cis-chlordane and trans-chlordane. GC/APCI/MS/MS and GC/HRMS were also compared by performing analysis on 75 human serum samples together with eight QA/QC serum samples. The comparison between GC/APCI/MS/MS system and GC/HRMS system for 16 of the targeted compounds was carried out. No statistically significant difference was discovered. Due to increased sensitivity and user friendly operation under atmospheric pressure, GC/APCI/MS/MS is a powerful alternative technique that can easily meet the specification of GC/HRMS.

Place, publisher, year, edition, pages
Amsterdam, Netherlands: Elsevier, 2016
Keywords
PCBs, OCPs, atmospheric pressure chemical ionization (APCI), triple quadrupole mass spectrometry (MS/MS), high resolution mass spectrometry (GC/HRMS), human serum
National Category
Chemical Sciences
Research subject
Analytical Chemistry; Environmental Chemistry; Enviromental Science
Identifiers
urn:nbn:se:liu:diva-193758 (URN)10.1016/j.chroma.2016.05.030 (DOI)000378182800010 ()27236485 (PubMedID)2-s2.0-84969722268 (Scopus ID)
Note

Funding Agency:

China Scholarship Council (CSC) under the Grant CSC 201206400003

Available from: 2023-05-16 Created: 2023-05-16 Last updated: 2023-05-29
Ericson Jogsten, I., Wang, T., Geng, D. & Roos, A. (2016). Temporal trends of persistent organochlorine and bromine compounds in ringed seals from the Baltic Sea (Phoca hispida baltica) from year 1974 to 2015. Paper presented at 36th International Symposium on Halogenated Persistent Organic Pollutants, Dioxin 2016, Florence, Italy, August 28 - September 2, 2016. Organohalogen Compounds, 78
Open this publication in new window or tab >>Temporal trends of persistent organochlorine and bromine compounds in ringed seals from the Baltic Sea (Phoca hispida baltica) from year 1974 to 2015
2016 (English)In: Organohalogen Compounds, ISSN 1026-4892, Vol. 78Article in journal (Refereed) Published
Place, publisher, year, edition, pages
Eco-Informa Press, 2016
National Category
Analytical Chemistry
Identifiers
urn:nbn:se:liu:diva-193751 (URN)
Conference
36th International Symposium on Halogenated Persistent Organic Pollutants, Dioxin 2016, Florence, Italy, August 28 - September 2, 2016
Available from: 2023-05-16 Created: 2023-05-16 Last updated: 2023-05-25Bibliographically approved
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Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0002-6330-789X

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