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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Quantitative analysis of unconjugated and total bisphenol A in human urine using solid-phase extraction and UPLC-MS/MS: Method implementation, method qualification and troubleshooting
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Quantitative analysis of unconjugated and total bisphenol A in human urine using solid-phase extraction and UPLC-MS/MS: Method implementation, method qualification and troubleshooting

机译:固相萃取和UPLC-MS / MS对人尿中非共轭双酚A和总双酚A的定量分析:方法实施,方法鉴定和故障排除

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摘要

The aim of the presented investigation was to document challenges encountered during implementation and qualification of a method for bisphenol A (BPA) analysis and to develop and discuss precautions taken to avoid and to monitor contamination with BPA during sample handling and analysis. Previously developed and published HPLC-MS/MS methods for the determination of unconjugated BPA (Markham et al. Journal of Analytical Toxicology, 34 (2010) 293-303) [17] and total BPA (Markham et al. Journal of Analytical Toxicology, 38 (2014) 194-203) [20] in human urine were combined and transferred into another laboratory. The initial method for unconjugated BPA was developed and evaluated in two independent laboratories simultaneously. The second method for total BPA was developed and evaluated in one of these laboratories to conserve resources. Accurate analysis of BPA at sub-ppb levels is a challenging task as BPA is a widely used material and is ubiquitous in the environment at trace concentrations. Propensity for contamination of biological samples with BPA is reported in the literature during sample collection, storage, and/or analysis. Contamination by trace levels of BPA is so pervasive that even with extraordinary care, it is difficult to completely exclude the introduction of BPA into biological samples and, consequently, contamination might have an impact on BPA biomonitoring data. The applied UPLC-MS/MS method was calibrated from 0.05 to 25 ng/ml. The limit of quantification was 0.1 ng/ml for unconjugated BPA and 0.2 ng/ml for total BPA, respectively, in human urine. Finally, the method was applied to urine samples derived from 20 volunteers. Overall, BPA can be analyzed in human urine with acceptable recovery and repeatability if sufficient measures are taken to avoid contamination throughout the procedure from sample collection until UPLC-MS/MS analysis. (C) 2015 The Authors. Published by Elsevier B.V.
机译:本研究的目的是记录双酚A(BPA)分析方法的实施和鉴定过程中遇到的挑战,并制定和讨论为避免和监测样品处理和分析过程中BPA污染而采取的预防措施。先前开发和发布的用于测定未结合BPA的HPLC-MS / MS方法(Markham等,Journal of Analytical Toxicology,34(2010)293-303)[17]和总BPA(Markham等,Journal of Analytical Toxicology, 38(2014)194-203)[20]在人类尿液中合并并转移到另一个实验室。非结合双酚A的最初方法是在两个独立的实验室中同时开发和评估的。在其中一个实验室中开发并评估了总BPA的第二种方法,以节省资源。由于BPA是一种广泛使用的材料,并且在环境中以痕量浓度无处不在,因此准确分析亚ppb级别的BPA是一项艰巨的任务。在文献收集,存储和/或分析期间,文献报道了BPA污染生物样品的可能性。痕量BPA的污染非常普遍,以至于即使格外小心,也很难完全排除将BPA引入生物样品中的情况,因此,污染可能会对BPA生物监测数据产生影响。将应用的UPLC-MS / MS方法校准为0.05至25 ng / ml。人尿中未结合的BPA的定量限分别为0.1 ng / ml和总BPA的定量限为0.2 ng / ml。最后,该方法应用于来自20名志愿者的尿液样本。总体而言,如果采取了足够的措施避免从样品收集到UPLC-MS / MS分析的整个过程受到污染,则可以在人尿中分析BPA,并具有可接受的回收率和重复性。 (C)2015作者。由Elsevier B.V.发布

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