首页> 外文期刊>Analytical chemistry >Determination of 16 Phthalate Metabolites in Urine Using Automated Sample Preparation and On-line Preconcentration/High-Performance Liquid Chromatography/Tandem Mass Spectrometry
【24h】

Determination of 16 Phthalate Metabolites in Urine Using Automated Sample Preparation and On-line Preconcentration/High-Performance Liquid Chromatography/Tandem Mass Spectrometry

机译:使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

获取原文
获取原文并翻译 | 示例
           

摘要

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 μL), is sensitive (limits of detection range from 0.11 to 0.90 ng/mL), accurate (spiked recoveries are ~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.
机译:我们开发了一种在线固相萃取(SPE)方法,并结合了同位素稀释高效液相色谱/串联质谱(HPLC / MS / MS)和自动样品制备,以同时定量人类尿液中的16种邻苯二甲酸酯代谢物。该方法需要用于从尿液中初步富集邻苯二甲酸盐的二氧化硅基整体柱,以及用于色谱分离目标分析物的二氧化硅基常规分析柱。它使用少量尿液(100μL),灵敏(检测极限范围为0.11至0.90 ng / mL),准确(加标回收率约为100%),并且精确(日间和日内变异系数< 10%)。该方法不耗费劳力,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,因此涉及的样品处理量最少,从而最大程度地减少了对有害化学物质的暴露。该方法已在加标,合并的尿液样本以及43名未曾接触邻苯二甲酸盐的成年人的尿液样本中得到验证。这种分析方法的高灵敏度和高通量(HPLC运行时间,包括预浓缩步骤为27分钟),结合了易用性和有效的自动样品制备程序,使其适用于大型流行病学研究,以评估人体暴露的患病率邻苯二甲酸盐。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号