B'Hymer C
U.S. Department of Health and Human Services, Centers for Disease Control, National Institute for Occupational Safety and Health, Division of Applied Research and Technology, Taft Laboratory C-23, 4676 Columbia Parkway, Cincinnati, OH 45226, USA.
J Chromatogr Sci. 2011 Aug;49(7):547-53. doi: 10.1093/chrsci/49.7.547.
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 triple-quadrupole 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.
本文介绍并评估了一种采用高效液相色谱-串联质谱法(HPLC-MS-MS)测定人尿中S-苄基硫醚氨酸(S-BMA)和S-苯基硫醚氨酸(S-PMA)的方法。这两种化合物分别作为甲苯和苯暴露的生物标志物,对职业健康具有重要意义。甲苯被广泛用作溶剂,而苯对健康的危害已得到充分证实。优化后的尿液样品制备方案包括固相萃取(SPE),随后用丙酮洗涤。色谱分析采用反相梯度系统,在负离子模式下使用电喷雾电离,并配备三重四极杆质谱检测器。通过对加标人尿和合成尿替代物的一系列回收率研究,证明了该方法的准确性和精密度。两种分析物在1、2、6、8和30 ng/mL的加标水平下,平均回收率(准确度)在99%至110%之间。尿液中两种分析物在每个浓度水平下多个样品(n=9)的相对标准偏差(%RSD)所测得的精密度为5.3%或更低。S-BMA和S-PMA的检测限约为0.2 ng/mL。本文讨论了这些数据、其他品质因数以及其他因素,如电喷雾电离源的离子抑制。