Validation of an HPLC-MS-MS Method for the Determination of Urinary S-Benzylmercapturic Acid and S-Phenylmercapturic Acid

被引:14
|
作者
B'Hymer, C. [1 ]
机构
[1] NIOSH, US Dept HHS, Ctr Dis Control, Div Appl Res & Technol,Taft Lab C 23, Cincinnati, OH 45226 USA
关键词
CHROMATOGRAPHY-MASS SPECTROMETRY; OCCUPATIONAL-EXPOSURE; INDUSTRIAL-CHEMICALS; BENZENE METABOLITES; LC-MS; LIQUID; BIOMARKERS; TOLUENE; QUANTIFICATION; SOLVENTS;
D O I
10.1093/chrsci/49.7.547
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high-performance liquid chromatography-tandem mass spectrometric (HPLC-MS-MS) method is presented and evaluated for the determination of S-benzylmercapturic acid (S-BMA) and S-phenylmercapturic acid (S-PMA) in human urine. Both of these compounds are important for occupational health owing to their use as biomarkers of exposure to toluene and benzene, respectively. Toluene is used extensively as a solvent, and the health hazards of benzene have been well established. The optimized urine sample preparation scheme consists of solid-phase extraction (SPE) followed by an acetone wash. The chromatographic analysis consists of a reversed-phase gradient system, which uses electrospray ionization in negative-ion mode with a triplequadrupole mass spectrometric detector. Accuracy and precision of this method are demonstrated by a series of recovery studies of spiked human urine and synthetic urine substitute. Spike levels at 1, 2, 6, 8, and 30 ng/mL for both analytes demonstrate average recoveries (accuracy) ranging from 99 to 110%. Precision as measured by the relative standard deviation (%RSD) of multiple samples (n = 9) at each concentration level was 5.3% or less for both analytes in urine. The limit of detection (LOD) is approximately 0.2 ng/mL for S-BMA and S-PMA. This data, other figures of merit and other factors, such as ion suppression of the electrospray ionization source, are discussed.
引用
收藏
页码:547 / 553
页数:7
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