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运用高分辨精确质量质谱法研究氯化石蜡的体外生物转化及潜在转化产物的评估。

In vitro biotransformation and evaluation of potential transformation products of chlorinated paraffins by high resolution accurate mass spectrometry.

机构信息

Queensland Alliance for Environmental Health Science (QAEHS), The University of Queensland, 4102 Brisbane, Australia.

Department of Environment and Health, Vrije Universiteit, De Boelelaan 1087, 1081 HV Amsterdam, The Netherlands.

出版信息

J Hazard Mater. 2021 Mar 5;405:124245. doi: 10.1016/j.jhazmat.2020.124245. Epub 2020 Oct 10.

Abstract

Chlorinated paraffins (CPs) are high production chemicals, which leads to their ubiquitous presence in the environment. To date, few studies have measured CPs in humans and typically at relatively low concentrations, despite indications that exposure may be high compared to various persistent organic pollutants. The aim of this study is to investigate the in vitro biotransformation of CPs by human liver fractions. We determined the changes of the CP concentrations after the enzymatic transformation with human liver microsomes using a two-tiered in vitro approach. CP concentrations decreased with human liver microsomes, with the decreases of 33-94% after incubating with different groups of enzymes for 2 h. The profiles of CP rapidly shifted after the incubation with human liver microsomes. In addition, the concentrations of CPs and the biotransformation products were tentatively measured using high-resolution mass spectrometric analysis, including very short CP (carbon chain length <10), alcohols, ketones, and carboxylic acids. C‒C bond cleavage is a potential transformation pathway for CPs, and ketones are potential products of CP biotransformation, especially for long-chain CPs (C). The ketone products may be investigated as CP exposure biomarker in biomonitoring studies.

摘要

氯化石蜡(CPs)是一种高产量的化学品,因此在环境中普遍存在。迄今为止,很少有研究测量过人体内的 CPs,而且通常浓度相对较低,尽管有迹象表明,与各种持久性有机污染物相比,接触 CPs 的可能性很高。本研究旨在研究人肝匀浆对 CPs 的体外生物转化。我们使用双层体外方法,用人肝微粒体测定了 CPs 在酶转化后的浓度变化。用不同组的酶孵育 2 小时后,CP 浓度随着人肝微粒体的作用而降低,降幅为 33%-94%。CP 与肝微粒体孵育后,CP 的图谱迅速发生变化。此外,还使用高分辨率质谱分析,包括非常短链的 CP(碳链长度 <10)、醇、酮和羧酸,对 CPs 和生物转化产物的浓度进行了初步测量。CP 可能发生 C-C 键断裂的转化途径,酮类是 CP 生物转化的潜在产物,特别是对于长链 CP(C)。酮类产物可作为生物监测研究中 CP 暴露的生物标志物进行研究。

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