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采用手性液相色谱-串联质谱检测法对环境样品中的人用和兽用药品及其代谢物进行多残留对映体分析。

Multi-residue enantiomeric analysis of human and veterinary pharmaceuticals and their metabolites in environmental samples by chiral liquid chromatography coupled with tandem mass spectrometry detection.

作者信息

Camacho-Muñoz Dolores, Kasprzyk-Hordern Barbara

机构信息

Department of Chemistry, University of Bath, Bath, BA2 7AY, UK.

出版信息

Anal Bioanal Chem. 2015 Dec;407(30):9085-104. doi: 10.1007/s00216-015-9075-6. Epub 2015 Oct 13.

Abstract

Enantiomeric profiling of chiral pharmacologically active compounds (PACs) in the environment has hardly been investigated. This manuscript describes, for the first time, a multi-residue enantioselective method for the analysis of human and veterinary chiral PACs and their main metabolites from different therapeutic groups in complex environmental samples such as wastewater and river water. Several analytes targeted in this paper have not been analysed in the environment at enantiomeric level before. These are aminorex, carboxyibuprofen, carprofen, cephalexin, 3-N-dechloroethylifosfamide, 10,11-dihydro-10-hydroxycarbamazepine, dihydroketoprofen, fenoprofen, fexofenadine, flurbiprofen, 2-hydroxyibuprofen, ifosfamide, indoprofen, mandelic acid, 2-phenylpropionic acid, praziquantel and tetramisole. The method is based on chiral liquid chromatography utilising a chiral α1-acid glycoprotein column and tandem mass spectrometry detection. Excellent chromatographic separation of enantiomers (Rs≥1.0) was achieved for chloramphenicol, fexofenadine, ifosfamide, naproxen, tetramisole, ibuprofen and their metabolites: aminorex and dihydroketoprofen (three of four enantiomers), and partial separation (Rs = 0.7-1.0) was achieved for ketoprofen, praziquantel and the following metabolites: 3-N-dechloroethylifosfamide and 10,11-dihydro-10-hydroxycarbamazepine. The overall performance of the method was satisfactory for most of the compounds targeted. Method detection limits were at low nanogram per litre for surface water and effluent wastewater. Method intra-day precision was on average under 20% and sample pre-concentration using solid phase extraction yielded recoveries >70% for most of the analytes. This novel, selective and sensitive method has been applied for the quantification of chiral PACs in surface water and effluent wastewater providing excellent enantioresolution of multicomponent mixtures in complex environmental samples. It will help with better understanding of the role of individual enantiomers in the environment and will enable more accurate environmental risk assessment.

摘要

环境中手性药理活性化合物(PACs)的对映体分析几乎未被研究过。本文首次描述了一种多残留对映体选择性方法,用于分析复杂环境样品(如废水和河水)中来自不同治疗组的人类和兽用手性PACs及其主要代谢物。本文所针对的几种分析物此前尚未在环境中进行对映体水平的分析。这些分析物包括阿米雷司、羧基布洛芬、卡洛芬、头孢氨苄、3-N-去氯乙基异环磷酰胺、10,11-二氢-10-羟基卡马西平、二氢酮洛芬、非诺洛芬、非索非那定、氟比洛芬、2-羟基布洛芬、异环磷酰胺、吲哚洛芬、扁桃酸、2-苯丙酸、吡喹酮和四咪唑。该方法基于使用手性α1-酸性糖蛋白柱的手性液相色谱和串联质谱检测。氯霉素、非索非那定、异环磷酰胺、萘普生、四咪唑、布洛芬及其代谢物:阿米雷司和二氢酮洛芬(四种对映体中的三种)实现了对映体的出色色谱分离(Rs≥1.0),酮洛芬、吡喹酮及其以下代谢物:3-N-去氯乙基异环磷酰胺和10,11-二氢-10-羟基卡马西平实现了部分分离(Rs = 0.7 - 1.0)。对于大多数目标化合物,该方法的整体性能令人满意。地表水和污水处理厂出水的方法检测限为低纳克每升。方法日内精密度平均低于20%,使用固相萃取进行样品预浓缩,大多数分析物的回收率>70%。这种新颖、选择性和灵敏的方法已应用于地表水和污水处理厂出水中手性PACs的定量分析,在复杂环境样品中提供了多组分混合物出色的对映体分离度。它将有助于更好地理解单个对映体在环境中的作用,并能够进行更准确的环境风险评估。

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