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采用填充型多壁碳纳米管固相萃取与液相色谱-四极杆线性离子阱质谱联用测定河水和废水中的药物。

Determination of drugs in river and wastewaters using solid-phase extraction by packed multi-walled carbon nanotubes and liquid chromatography-quadrupole-linear ion trap-mass spectrometry.

机构信息

Department of Chemistry, University of Oran, Oran, Algeria.

出版信息

J Chromatogr A. 2013 Jul 5;1297:17-28. doi: 10.1016/j.chroma.2013.05.002. Epub 2013 May 10.

Abstract

The present paper describes a solid-phase extraction by packed multi-walled carbon nanotubes, followed by liquid chromatography-mass spectrometry, method for the determination of some of the most consumed drugs including four β-blockers and eight non-steroidal anti-inflammatory drugs, in river and wastewater samples. High extraction efficiency was found for most drugs due to the large specific surface area and high adsorption capacity of this nanomaterial compared with other conventional solid-phase extraction sorbents, and matrix effect was present only for two of the twelve studied drugs. Only 20mg of carbon nanotubes was enough to preconcentrate the analytes with recoveries from 68% to 107% for most of them. The pharmaceuticals were analyzed by liquid chromatography coupled to a hybrid triple quadrupole-linear ion trap-mass spectrometer at ultra-trace levels. Data acquisition was carried out in selected reaction monitoring mode, using two transitions for simultaneous identification and quantification of the analytes. Additionally, an information dependent acquisition scan was performed to carry out the identification of those analytes whose second transition was absent or was present at low intensity. The analytical performance of the whole method was evaluated in two environmental water matrices (river and wastewaters). Matrix effect was not found in river water, quantitation being carried out with calibration graphs built with solvent based standard. On the contrary, matrix effect was present in wastewater for some of the target drugs and, therefore, quantitation was carried out using the standard addition method. Limits of detection and quantitation in river waters were in the range of 9-36 and 23-121ngL(-1), respectively and the relative standard deviation of the full method was less than 17%. The proposed methodology was applied to the analysis of three river water and two wastewater (influent and effluent) samples, all of them from Almería (Spain). Some pharmaceuticals were found in river water at concentration levels near to or lower than their quantitation limits, whereas the most consumed pharmaceuticals were found at high concentration levels in influent wastewater and were not detected or were found at lower levels in the effluent wastewater sample.

摘要

本文描述了一种基于填充多壁碳纳米管的固相萃取,结合液相色谱-质谱法,用于测定河流水和废水中的一些最常使用的药物,包括四种β受体阻滞剂和八种非甾体抗炎药。与其他常规固相萃取吸附剂相比,由于这种纳米材料具有较大的比表面积和较高的吸附能力,大多数药物的萃取效率都很高,而且只有两种研究药物存在基质效应。仅需 20mg 的碳纳米管即可对分析物进行预浓缩,大多数药物的回收率在 68%至 107%之间。使用混合三重四极杆-线性离子阱-质谱仪在超痕量水平下对药物进行分析。数据采集采用选择反应监测模式,使用两个跃迁对分析物进行同时鉴定和定量。此外,还进行了信息依赖采集扫描,以鉴定那些第二个跃迁不存在或强度较低的分析物。该方法的整个分析性能在两种环境水样(河水和废水)中进行了评估。在河水中未发现基质效应,定量采用基于溶剂的标准曲线进行。相反,在废水中,一些目标药物存在基质效应,因此采用标准添加法进行定量。在河水中,检测限和定量限分别在 9-36 和 23-121ng/L 范围内,全方法的相对标准偏差小于 17%。该方法应用于 3 个河水和 2 个废水(进水和出水)样品的分析,所有样品均来自西班牙阿尔梅里亚。在河水中发现了一些接近或低于定量限的药物,而在进水废水中发现了最常使用的药物,浓度较高,在出水废水中则未检测到或浓度较低。

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