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一种评估人类对手性化学物质暴露的生物标志物选择的新方法:以甲卡西酮为例。

A new approach towards biomarker selection in estimation of human exposure to chiral chemicals: a case study of mephedrone.

机构信息

Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, United Kingdom.

Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Saarland University, Homburg(Saar), 66421, Germany.

出版信息

Sci Rep. 2017 Nov 2;7(1):13009. doi: 10.1038/s41598-017-12581-3.

Abstract

Wastewater-based epidemiology is an innovative approach to estimate public health status using biomarker analysis in wastewater. A new compound detected in wastewater can be a potential biomarker of an emerging trend in public health. However, it is currently difficult to select new biomarkers mainly due to limited human metabolism data. This manuscript presents a new framework, which enables the identification and selection of new biomarkers of human exposure to drugs with scarce or unknown human metabolism data. Mephedrone was targeted to elucidate the assessment of biomarkers for emerging drugs of abuse using a four-step analytical procedure. This framework consists of: (i) identification of possible metabolic biomarkers present in wastewater using an in-vivo study; (ii) verification of chiral signature of the target compound; (iii) confirmation of human metabolic residues in in-vivo/vitro studies and (iv) verification of stability of biomarkers in wastewater. Mephedrone was selected as a suitable biomarker due to its high stability profile in wastewater. Its enantiomeric profiling was studied for the first time in biological and environmental matrices, showing stereoselective metabolism of mephedrone in humans. Further biomarker candidates were also proposed for future investigation: 4'-carboxy-mephedrone, 4'-carboxy-normephedrone, 1-dihydro-mephedrone, 1-dihydro-normephedrone and 4'-hydroxy-normephedrone.

摘要

基于污水的流行病学是一种使用污水中的生物标志物分析来评估公共卫生状况的创新方法。污水中检测到的新化合物可能是公共卫生新趋势的潜在生物标志物。然而,由于人类代谢数据有限,目前很难选择新的生物标志物。本文提出了一种新的框架,该框架能够识别和选择人类暴露于药物的新生物标志物,这些药物的人类代谢数据稀缺或未知。以 4-甲卡西酮为例,阐述了使用四步分析程序评估新滥用药物生物标志物的方法。该框架包括:(i)使用体内研究确定污水中存在的可能代谢生物标志物;(ii)验证目标化合物的手性特征;(iii)在体内/体外研究中确认人类代谢残留物;(iv)验证生物标志物在污水中的稳定性。4-甲卡西酮由于其在污水中的高稳定性而被选为合适的生物标志物。首次在生物和环境基质中研究了其对映体分布,显示了 4-甲卡西酮在人体中的立体选择性代谢。还提出了其他生物标志物候选物供未来研究:4'-羧基-4-甲卡西酮、4'-羧基-去甲麻黄碱、1-二氢-4-甲卡西酮、1-二氢-去甲麻黄碱和 4'-羟基-去甲麻黄碱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/065b/5693930/b477ab21b14f/41598_2017_12581_Fig1_HTML.jpg

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