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采用自动样品制备和在线预浓缩/高效液相色谱/串联质谱法测定尿液中的16种邻苯二甲酸酯代谢物。

Determination of 16 phthalate metabolites in urine using automated sample preparation and on-line preconcentration/high-performance liquid chromatography/tandem mass spectrometry.

作者信息

Kato Kayoko, Silva Manori J, Needham Larry L, Calafat Antonia M

机构信息

Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Hwy, Mailstop F17, Atlanta, Georgia 30341, USA.

出版信息

Anal Chem. 2005 May 1;77(9):2985-91. doi: 10.1021/ac0481248.

Abstract

We developed an on-line solid-phase extraction (SPE) method, coupled with isotope dilution high-performance liquid chromatography/tandem mass spectrometry (HPLC/MS/MS) and with automated sample preparation, to simultaneously quantify 16 phthalate metabolites in human urine. The method requires a silica-based monolithic column for the initial preconcentration of the phthalate metabolites from the urine and a silica-based conventional analytical column for the chromatographic separation of the analytes of interest. It uses small amounts of urine (100 microL), is sensitive (limits of detection range from 0.11 to 0.90 ng/mL), accurate (spiked recoveries are approximately 100%), and precise (the inter- and intraday coefficients of variation are <10%). The method is not labor intensive, and, because pretreatment of the urine samples was performed automatically using an HPLC autosampler, involves minimal sample handling, thus minimizing exposure to hazardous chemicals. The method was validated on spiked, pooled urine samples and on urine samples from 43 adults with no known exposure to phthalates. The high sensitivity and high throughput (HPLC run time, including the preconcentration step, is 27 min) of this analytical method combined with the ease of use and effective automated sample preparation procedure make it suitable for large epidemiological studies to evaluate the prevalence of human exposure to phthalates.

摘要

我们开发了一种在线固相萃取(SPE)方法,结合同位素稀释高效液相色谱/串联质谱(HPLC/MS/MS)以及自动化样品制备,用于同时定量人尿中的16种邻苯二甲酸酯代谢物。该方法需要一根基于硅胶的整体柱用于从尿液中初步预富集邻苯二甲酸酯代谢物,以及一根基于硅胶的常规分析柱用于对目标分析物进行色谱分离。它使用少量尿液(100微升),灵敏度高(检测限范围为0.11至0.90纳克/毫升),准确度高(加标回收率约为100%),精密度高(日内和日间变异系数<10%)。该方法无需大量人力,并且由于尿液样品的预处理是使用HPLC自动进样器自动进行的,样品处理量极少,从而将接触有害化学物质的风险降至最低。该方法在加标混合尿液样品以及43名无已知邻苯二甲酸酯暴露史的成年人的尿液样品上进行了验证。这种分析方法的高灵敏度和高通量(包括预富集步骤在内的HPLC运行时间为27分钟),再加上易于使用和有效的自动化样品制备程序,使其适用于大规模流行病学研究,以评估人类接触邻苯二甲酸酯的普遍性。

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