Biological monitoring of 3-phenoxybenzoic acid in urine by an enzyme-linked immunosorbent assay

被引:17
作者
Chuang, Jane C. [1 ]
Van Emon, Jeanette M. [2 ]
Trejo, Raquel M. [1 ]
Durnford, Joyce [1 ]
机构
[1] Battelle Mem Inst, Columbus, OH 43201 USA
[2] US EPA, Natl Exposure Res Lab, Las Vegas, NV 89193 USA
关键词
3-Phenoxybenzoic acid; Biomonitoring; Urinary biomarker; Enzyme-linked immunosorbent assay; PYRETHROID INSECTICIDES; METABOLITES; EXPOSURE; IMMUNOASSAY;
D O I
10.1016/j.talanta.2010.07.077
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An enzyme-linked immunosorbent assay (ELISA) method was employed for determination of the pyrethroid biomarker, 3-phenoxybenzoic acid (3-PBA) in human urine samples. The optimized coating antigen concentration was 0.5 ng/mL with a dilution of 1:4000 for the 3-PBA antibody and 1:6000 for the enzyme conjugate. Urine samples were hydrolyzed with concentrated hydrochloric acid; extracted with dichloromethane and solvent-exchanged into a methanol/buffer solution, prior to analysis in a 96-microwell plate immunoassay. Quantitative recoveries of 3-PBA were obtained for fortified urine samples by ELISA (92 +/- 18%) as well as by gas chromatography/mass spectrometry (GC/MS) (90 +/- 13%). The overall method precision of these samples was within +/- 20% for both the ELISA and GC/MS methods. Analytical results from over one hundred urine samples showed that the ELISA and GC/MS data were highly correlated, with a correlation coefficient of 0.95. At the 10 ng/mL comparative concentration level, the false positive rate was 0% and the false negative rate was 0.8% for ELISA when using GC/MS as the reference method. The ELISA method has a suitable low detection limit for 3-PBA to assess pyrethroid exposures in non-occupational settings. (C) 2010 Elsevier B.V. All rights reserved.
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页码:1317 / 1323
页数:7
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