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采用同位素稀释技术和串联质谱法测定人尿中的农药代谢物。

Determination of pesticide metabolites in human urine using an isotope dilution technique and tandem mass spectrometry.

作者信息

Hill R H, Shealy D B, Head S L, Williams C C, Bailey S L, Gregg M, Baker S E, Needham L L

机构信息

National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341-3724, USA.

出版信息

J Anal Toxicol. 1995 Sep;19(5):323-9. doi: 10.1093/jat/19.5.323.

Abstract

A method that measures 12 analytes in urine and reflects possible exposure to pesticides was developed. The sample preparation involves enzyme hydrolysis and solvent extraction through the use of laboratory robotics, followed by phase-transfer catalysis derivatization and silica cleanup. Samples are analyzed by capillary gas chromatography and tandem mass spectrometry using an isotope dilution technique with 13C-labeled internal standards. The limit of detection is 1 microgram/L (1 part per billion) for most analytes, and most analytes have a linear response up to 100 micrograms/L. The precision of the method is reflected in the variation observed in quality control materials over 33 months; the variation averaged 17% for these analytes. On the basis of the detectable analyte levels of unspiked urine samples collected from unexposed volunteers, this method can be used to measure the low levels necessary for establishing reference range values of the selected pesticides or metabolites.

摘要

开发了一种可测定尿液中12种分析物并反映可能接触农药情况的方法。样品制备包括酶水解和通过实验室机器人技术进行溶剂萃取,随后进行相转移催化衍生化和硅胶净化。使用含13C标记内标的同位素稀释技术,通过毛细管气相色谱和串联质谱对样品进行分析。大多数分析物的检测限为1微克/升(十亿分之一),并且大多数分析物在高达100微克/升的浓度范围内具有线性响应。该方法的精密度通过33个月期间质量控制材料中观察到的变化来体现;这些分析物的变化平均为17%。基于从未接触志愿者收集的未加标尿液样品中可检测到的分析物水平,该方法可用于测量确定所选农药或代谢物参考范围值所需的低水平。

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