Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ay05089c
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dc.titleUltra-performance liquid chromatographic assay coupled with two-dimensional separation for spectrometric determination of urinary S-phenylmercapturic acid
dc.contributor.authorLee, B.L.
dc.contributor.authorOng, H.Y.
dc.contributor.authorChia, S.E.
dc.contributor.authorOng, C.N.
dc.date.accessioned2014-11-26T07:49:16Z
dc.date.available2014-11-26T07:49:16Z
dc.date.issued2011-09
dc.identifier.citationLee, B.L., Ong, H.Y., Chia, S.E., Ong, C.N. (2011-09). Ultra-performance liquid chromatographic assay coupled with two-dimensional separation for spectrometric determination of urinary S-phenylmercapturic acid. Analytical Methods 3 (9) : 2025-2031. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ay05089c
dc.identifier.issn17599660
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/109722
dc.description.abstractA gradient ultra-performance liquid chromatographic (UPLC) assay coupled with the two dimensional separation and diode array detection method was developed to determine S-phenylmercapturic acid (SPMA), a specific urinary metabolite of benzene. Gradient separation was performed on two C18 core-shell columns (2.6 and 1.7 μm, 50 × 2.1 mm i.d.) maintained at 40 and 20 °C. Among various solvents evaluated, dichloromethane which offered >85% recovery rates of both SPMA and d-benzylmercapturic acid (internal standard) was used for extraction. The yield of free-SPMA was maximized by hydrolyzing 200 μL of urine with 20 μL of 6 M HCl prior to dichloromethane extraction. The limit of detection was 1 μg L-1(s/n = 5) and the limit of quantification was 2 μg L-1. Using our method, a correlation of 0.99 was obtained with 10 specimens (range, 1.7 to 182 μg L-1) from the German External Quality Assessment Scheme. Among the 75 non-occupational exposure individuals, 61 (81%) had SPMA levels below the LOQ. Among the 26 male petroleum workers, 5 who were exposed to
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1ay05089c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentEPIDEMIOLOGY & PUBLIC HEALTH
dc.description.doi10.1039/c1ay05089c
dc.description.sourcetitleAnalytical Methods
dc.description.volume3
dc.description.issue9
dc.description.page2025-2031
dc.identifier.isiut000294472900014
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