a Department of Environmental Health , Rollins School of Public Health, Emory University , Atlanta , Georgia , USA.
c ORISE, Centers for Disease Control and Prevention , Atlanta , Georgia , USA.
Crit Rev Anal Chem. 2016;46(2):93-105. doi: 10.1080/10408347.2014.980775.
The ability to quantify levels of target analytes in biological samples accurately and precisely in biomonitoring involves the use of highly sensitive and selective instrumentation such as tandem mass spectrometers and a thorough understanding of highly variable matrix effects. Typically, matrix effects are caused by co-eluting matrix components that alter the ionization of target analytes as well as the chromatographic response of target analytes, leading to reduced or increased sensitivity of the analysis. Thus, before the desired accuracy and precision standards of laboratory data are achieved, these effects must be characterized and controlled. Here we present our review and observations of matrix effects encountered during the validation and implementation of tandem mass spectrometry-based analytical methods. We also provide systematic, comprehensive laboratory strategies needed to control challenges posed by matrix effects in order to ensure delivery of the most accurate data for biomonitoring studies assessing exposure to environmental toxicants.
准确、精确地定量生物样本中目标分析物的能力涉及使用高度灵敏和选择性的仪器,如串联质谱仪,以及对高度可变的基质效应有透彻的了解。通常,基质效应是由共洗脱的基质成分引起的,这些成分会改变目标分析物的离子化以及目标分析物的色谱响应,从而导致分析的灵敏度降低或增加。因此,在达到实验室数据所需的准确性和精密度标准之前,必须对这些效应进行特征描述和控制。在这里,我们回顾并观察了在基于串联质谱的分析方法的验证和实施过程中遇到的基质效应。我们还提供了系统、全面的实验室策略,以控制基质效应带来的挑战,从而确保为评估环境毒物暴露的生物监测研究提供最准确的数据。