Holler J S, Fast D M, Hill R H, Cardinali F L, Todd G D, McCraw J M, Bailey S L, Needham L L
Division of Environmental Health Laboratory Sciences, Centers for Disease Control, U.S. Department of Health and Human Services, Atlanta, Georgia 30333.
J Anal Toxicol. 1989 May-Jun;13(3):152-7. doi: 10.1093/jat/13.3.152.
We have developed a method for determining selected chlorinated phenols and phenoxy herbicides in urine. The process of preparing the samples includes acid hydrolysis, extraction with benzene, derivatization with diazoethane, and column chromatography cleanup. We quantify the more volatile compounds by using capillary column gas chromatography/positive chemical ionization/mass spectrometry/mass spectrometry. Less volatile compounds are quantified by using electron capture negative chemical ionization in a single stage mass spectrometry mode. Quality control samples are included in each analytical run, and the results demonstrate that the analytical system is in control. Positive values for the target analytes are determined on the basis of appropriate relative retention time, a signal-to-noise ratio greater than 3:1, and a calculated concentration greater than 1 ppb. We determine the chlorine isotope ratios for each compound to assess the presence or absence of interferences. This analytical method has been applied in a case-control study of 199 individuals to examine exposure to the 12 target analytes.
我们开发了一种测定尿液中特定氯酚和苯氧基除草剂的方法。样品制备过程包括酸水解、用苯萃取、用重氮乙烷衍生化以及柱色谱净化。我们通过毛细管柱气相色谱/正化学电离/质谱/质谱对挥发性较强的化合物进行定量。挥发性较弱的化合物则通过单级质谱模式下的电子捕获负化学电离进行定量。每次分析运行都包含质量控制样品,结果表明分析系统处于受控状态。目标分析物的阳性值是根据适当的相对保留时间、大于3:1的信噪比以及计算浓度大于1 ppb来确定的。我们测定每种化合物的氯同位素比率以评估是否存在干扰。这种分析方法已应用于一项对199名个体的病例对照研究中,以检查对12种目标分析物的暴露情况。