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Global Profiling of Urinary Mercapturic Acids Using Integrated Library-Guided Analysis.
Xie, Zhengzhi; Chen, Jin Y; Gao, Hong; Keith, Rachel J; Bhatnagar, Aruni; Lorkiewicz, Pawel; Srivastava, Sanjay.
Affiliation
  • Xie Z; American Heart Association-Tobacco Regulation and Addiction Center, University of Louisville, Louisville, Kentucky 40202, United States.
  • Chen JY; Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky 40202, United States.
  • Gao H; Superfund Research Center, University of Louisville, Louisville, Kentucky 40202, United States.
  • Keith RJ; Division of Environmental Medicine, Department of Medicine, University of Louisville, Louisville, Kentucky 40202, United States.
  • Bhatnagar A; American Heart Association-Tobacco Regulation and Addiction Center, University of Louisville, Louisville, Kentucky 40202, United States.
  • Lorkiewicz P; Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky 40202, United States.
  • Srivastava S; Superfund Research Center, University of Louisville, Louisville, Kentucky 40202, United States.
Environ Sci Technol ; 57(29): 10563-10573, 2023 07 25.
Article in En | MEDLINE | ID: mdl-37432892
Urinary mercapturic acids (MAs) are often used as biomarkers for monitoring human exposures to occupational and environmental xenobiotics. In this study, we developed an integrated library-guided analysis workflow using ultraperformance liquid chromatography-quadrupole time-of-flight mass spectrometry. This method includes expanded assignment criteria and a curated library of 220 MAs and addresses the shortcomings of previous untargeted approaches. We employed this workflow to profile MAs in the urine of 70 participants─40 nonsmokers and 30 smokers. We found approximately 500 MA candidates in each urine sample, and 116 MAs from 63 precursors were putatively annotated. These include 25 previously unreported MAs derived mostly from alkenals and hydroxyalkenals. Levels of 68 MAs were comparable in nonsmokers and smokers, 2 MAs were higher in nonsmokers, and 46 MAs were elevated in smokers. These included MAs of polycyclic aromatic hydrocarbons and hydroxyalkenals and those derived from toxicants present in cigarette smoke (e.g., acrolein, 1,3-butadiene, isoprene, acrylamide, benzene, and toluene). Our workflow allowed profiling of known and unreported MAs from endogenous and environmental sources, and the levels of several MAs were increased in smokers. Our method can also be expanded and applied to other exposure-wide association studies.
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Full text: 1 Database: MEDLINE Main subject: Acetylcysteine / Tandem Mass Spectrometry Limits: Humans Language: En Journal: Environ Sci Technol Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Acetylcysteine / Tandem Mass Spectrometry Limits: Humans Language: En Journal: Environ Sci Technol Year: 2023 Type: Article Affiliation country: United States