Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55191
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dc.contributor.authorWarangkana Naksenen_US
dc.contributor.authorTippawan Prapamontolen_US
dc.contributor.authorAmpica Mangklabruksen_US
dc.contributor.authorSomporn Chantaraen_US
dc.contributor.authorPrasak Thavornyutikarnen_US
dc.contributor.authorMark G. Robsonen_US
dc.contributor.authorP. Barry Ryanen_US
dc.contributor.authorDana Boyd Barren_US
dc.contributor.authorParinya Panuweten_US
dc.date.accessioned2018-09-05T02:52:54Z-
dc.date.available2018-09-05T02:52:54Z-
dc.date.issued2016-07-01en_US
dc.identifier.issn1873376Xen_US
dc.identifier.issn15700232en_US
dc.identifier.other2-s2.0-84969593631en_US
dc.identifier.other10.1016/j.jchromb.2016.04.045en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84969593631&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55191-
dc.description.abstract© 2016 Elsevier B.V. Organophosphate (OP) pesticides are widely used for crop protection in many countries including Thailand. Aside from causing environmental contamination, they affect human health especially by over-stimulating of the neurotransmission system. OP pesticides, as with other non-persistent pesticides, degrade quickly in the environment as well as are metabolized quite rapidly in humans. Assessing human exposures to these compounds requires analytical methods that are sensitive, robust, and most importantly, suitable for specific laboratory settings. The aim of this study was to develop and validate an analytical method for measuring 11 OP pesticide residues in human plasma and breast milk. Analytes in both plasma and breast milk samples were extracted with acetone and methylene chloride, cleaned-up using aminopropyl solid phase extraction cartridges, and analyzed by gas chromatography with flame photometric detection. The optimized method exhibited good linearity, with the coefficients of determination of 0.996-0.999 and <7% error about the slope. Extraction recoveries from spiked plasma and breast milk samples at low and medium concentrations (0.8-5.0 and 1.6-10 ng mL-1, respectively) ranged from 59.4% (ethion) to 94.0% (chlorpyrifos). Intra-batch and inter-batch precisions ranged from 2.3-18.9% and 5.8-19.5%, respectively. Method detection limits of plasma and breast milk ranged from 0.18-1.36 and 0.09-2.66 ng mL-1, respectively. We analyzed 63 plasma and 30 breastmilk samples collected from farmworkers in Chiang Mai Province to determine the suitability of this method for occupational exposure assessment. Of the 11 pesticides measured, seven were detected in plasma samples and five were detected in breast milk samples. Mass spectrometry was used to confirm results. Overall, this method is rapid and reliable. It offers the laboratories with limited access to mass spectrometry a capacity to investigate levels OP pesticides in plasma and breastmilk in those occupationally exposed for health risk assessment.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleA single method for detecting 11 organophosphate pesticides in human plasma and breastmilk using GC-FPDen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciencesen_US
article.volume1025en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsRutgers, The State University of New Jerseyen_US
article.stream.affiliationsRollins School of Public Healthen_US
article.stream.affiliationsnullen_US
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