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高效液相色谱法对手性药物氟西汀和去甲氟西汀在废水中的对映体定量分析。

Enantioselective quantification of fluoxetine and norfluoxetine by HPLC in wastewater effluents.

机构信息

CESPU, Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde, R. Central de Gandra, 1317, 4585-116 Gandra PRD, Paredes, Portugal; CBQF - Centro de Biotecnologia e Química Fina - Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Dr. António Bernardino Almeida, 4200-072 Porto, Portugal; Centro de Química Medicinal da Universidade do Porto (CEQUIMED-UP), Rua de Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.

出版信息

Chemosphere. 2014 Jan;95:589-96. doi: 10.1016/j.chemosphere.2013.09.118. Epub 2013 Nov 1.

Abstract

Microbial degradation is the most important process to remove organic pollutants in Waste Water Treatment Plants. Regarding chiral compounds this process is normally enantioselective and needs the suitable analytical methodology to follow the removal of both enantiomers in an accurate way. Thus, this paper describes the development and validation of an enantioselective High Performance Liquid Chromatography with Fluorescence Detection (HPLC-FD) method for simultaneous analysis of fluoxetine (FLX) and norfluoxetine (NFLX) in wastewater effluents. Briefly, this method preconcentrated a small volume of wastewater samples (50 mL) on 500 mg Oasis MCX cartridges and used HPLC-FD with a vancomycin-based chiral stationary phase under reversed mode for analyses. The optimized mobile phase was EtOH/aqueous ammonium acetate buffer (92.5/7.5, v/v) at pH 6.8. The effect of EtOH percentage, buffer concentration, pH, column oven temperature and flow rate on chromatographic parameters was systematically investigated. The developed method was validated within the wastewater effluent used in microcosms laboratory assays. Linearity (R(2)>0.99), selectivity and sensitivity were achieved in the range of 4.0-60 ng mL(-1) for enantiomers of FLX and 2.0-30 ng mL(-1) for enantiomers of NFLX. The limits of detection were between 0.8 and 2.0 ng mL(-1) and the limits of quantification were between 2.0 and 4.0 ng mL(-1) for both enantiomers of FLX and the enantiomers of its demethylated metabolite NFLX. The validated method was successfully applied and proved to be robust to follow the degradation of both enantiomers of FLX in wastewater samples, during 46 days.

摘要

微生物降解是去除废水处理厂中有机污染物最重要的过程。对于手性化合物,该过程通常为对映选择性,需要合适的分析方法来准确跟踪两种对映体的去除。因此,本文描述了一种高效液相色谱-荧光检测(HPLC-FD)法的开发和验证,用于同时分析废水流出物中的氟西汀(FLX)和去甲氟西汀(NFLX)。简要地说,该方法在 500mg Oasis MCX 小柱上预浓缩 50mL 废水样品,并在反相模式下使用基于万古霉素的手性固定相和 HPLC-FD 进行分析。优化后的流动相为 EtOH/醋酸铵缓冲液(92.5/7.5,v/v),pH 值为 6.8。系统研究了 EtOH 百分比、缓冲液浓度、pH 值、柱温、流速对色谱参数的影响。所开发的方法在用于微宇宙实验室测定的废水流出物中进行了验证。FLX 和 NFLX 对映体的线性范围为 4.0-60ngmL(-1),选择性和灵敏度均达到 0.99 以上;FLX 和其去甲基代谢物 NFLX 对映体的检测限分别为 0.8-2.0ngmL(-1)和 2.0-4.0ngmL(-1)。验证后的方法成功应用于跟踪 FLX 两种对映体在废水样品中的降解过程,历时 46 天。

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