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采用液相色谱-高分辨质谱法对 17 种真菌毒素的 I 相和葡醛酸结合物 II 相代谢物进行表征。

Characterization of Phase I and Glucuronide Phase II Metabolites of 17 Mycotoxins Using Liquid Chromatography-High-Resolution Mass Spectrometry.

机构信息

Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montreal, QC H4B 1R6, Canada.

Centre for Biological Applications of Mass Spectrometry, Concordia University, 7141 Sherbrooke Street West, Montreal, QC H4B 1R6, Canada.

出版信息

Toxins (Basel). 2019 Jul 24;11(8):433. doi: 10.3390/toxins11080433.

Abstract

Routine mycotoxin biomonitoring methods do not include many mycotoxin phase I and phase II metabolites, which may significantly underestimate mycotoxin exposure especially for heavily metabolized mycotoxins. Additional research efforts are also needed to measure metabolites in vivo after exposure and to establish which mycotoxin metabolites should be prioritized for the inclusion during large-scale biomonitoring efforts. The objective of this study was to perform human in vitro microsomal incubations of 17 mycotoxins and systematically characterize all resulting metabolites using liquid chromatography-high-resolution mass spectrometry (LC-HRMS). The results obtained were then used to build a comprehensive LC-MS library and expand a validated 17-mycotoxin method for exposure monitoring to screening of additional 188 metabolites, including 100 metabolites reported for the first time. The final method represents one of the most comprehensive LC-HRMS methods for mycotoxin biomonitoring or metabolism/fate studies.

摘要

常规的真菌毒素生物监测方法并不包括许多真菌毒素 I 期和 II 期代谢物,这可能会大大低估真菌毒素暴露水平,尤其是对于代谢活跃的真菌毒素。此外,还需要开展更多的研究工作来测量暴露后体内的代谢物,并确定在大规模生物监测工作中应优先考虑哪些真菌毒素代谢物。本研究的目的是进行 17 种真菌毒素的人体体外微粒体孵育,并使用液相色谱-高分辨率质谱(LC-HRMS)系统地对所有生成的代谢物进行特征分析。然后,将获得的结果用于构建一个全面的 LC-MS 谱库,并扩展一个经过验证的用于暴露监测的 17 种真菌毒素方法,以筛查另外 188 种代谢物,其中包括 100 种首次报道的代谢物。最终方法代表了最全面的用于真菌毒素生物监测或代谢/命运研究的 LC-HRMS 方法之一。

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