Yang Xiangkun, Wu Xian, Brown Kyle A, Le Thao, Stice Steven L, Bartlett Michael G
Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, The University of Georgia, Athens, GA 30602-2352, United States.
Regenerative Bioscience Center, University of Georgia, Athens, GA 30602, United States.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Sep 15;1063:112-117. doi: 10.1016/j.jchromb.2017.08.010. Epub 2017 Aug 18.
A sensitive method to simultaneously quantitate chlorpyrifos, chlorpyrifos oxon and the detoxified product 3,5,6-trichloro-2-pyridinol (TCP) was developed using either liquid-liquid extraction for culture media samples, or protein precipitation for cell samples. Multiple reaction monitoring in positive ion mode was applied for the detection of chlorpyrifos and chlorpyrifos oxon, and selected ion recording in negative mode was applied to detect TCP. The method provided linear ranges from 5 to 500, 0.2-20 and 20-2000ng/mL for media samples and from 0.5-50, 0.02-2 and 2-200ng/million cells for CPF, CPO and TCP, respectively. The method was validated using selectivity, linearity, precision, accuracy, recovery, stability and dilution tests. All relative standard deviations (RSDs) and relative errors (REs) for QC samples were within 15% (except for LLOQ, within 20%). This method has been successfully applied to study the neurotoxicity and metabolism of chlorpyrifos in a human neuronal model.
开发了一种同时定量毒死蜱、毒死蜱氧磷和解毒产物3,5,6-三氯-2-吡啶醇(TCP)的灵敏方法,对于培养基样品采用液液萃取,对于细胞样品采用蛋白沉淀法。在正离子模式下进行多反应监测以检测毒死蜱和毒死蜱氧磷,在负离子模式下采用选择离子记录来检测TCP。该方法为培养基样品提供的线性范围分别为5至500、0.2至20和20至2000 ng/mL,对于毒死蜱、毒死蜱氧磷和TCP,分别为0.5至50、0.02至2和2至200 ng/百万细胞。通过选择性、线性、精密度、准确度、回收率、稳定性和稀释试验对该方法进行了验证。QC样品的所有相对标准偏差(RSD)和相对误差(RE)均在15%以内(除LLOQ外,在20%以内)。该方法已成功应用于研究毒死蜱在人神经元模型中的神经毒性和代谢。