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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of acidic drugs and caffeine in municipal wastewaters and receiving waters by gas chromatography-ion trap tandem mass spectrometry
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Determination of acidic drugs and caffeine in municipal wastewaters and receiving waters by gas chromatography-ion trap tandem mass spectrometry

机译:气相色谱-离子阱串联质谱法测定城市废水和接收水中的酸性药物和咖啡因

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Some aspects of both sample preparation and instrumental techniques for analysis of such acidic drugs as acetylsalicylic acid, ibuprofen, gemfibrozil, fenoprofen, naproxen, ketoprofen, and diclofenac, as well as caffeine in surface water and municipal wastewater have been studied and further developed. Water samples were filtered and target analytes were extracted by solid-phase extraction (SPE). Supelco LC-18 and Oasis HLB SPE cartridges were used to pre-concentrate samples for acidic drugs and caffeine, respectively. A methylation process was applied to acidic drugs prior to analysis while caffeine was analyzed directly. A method of gas chromatography-ion trap tandem mass spectrometry (IT-MS/MS) for analysis of the target acidic pharmaceuticals and caffeine is presented here in detail. Such parameters as collision-induced dissociation (CID) voltage, isolation time, excitation time, excitation storage level, and electron energy were adjusted in order to optimize the instrument analytical performance. After optimization, an instrument detection limit of 0.5-20 pg/mu L with signal-to-noise (S/N) not less than 5 was achieved for all target analytes. It was shown that this method has good linearity within the range of 10-2000 pg/mu L. The application of the optimized IT-MS/MS parameters conjointly with the sample preparation procedure resulted in method detection limits (MDLs) of 0.1-1.0 and 20 ng/L for the determination of acidic drugs and caffeine, respectively in such samples as surface water, effluent from municipal wastewater plants, as well as receiving waters. (c) 2006 Elsevier B.V. All rights reserved.
机译:研究和进一步开发了用于分析酸性药物如乙酰水杨酸,布洛芬,吉非贝齐,非诺洛芬,萘普生,酮洛芬和双氯芬酸以及咖啡因的地表水和市政废水的样品制备和仪器技术的某些方面。过滤水样品,并通过固相萃取(SPE)萃取目标分析物。 Supelco LC-18和Oasis HLB SPE柱分别用于预浓缩酸性药物和咖啡因的样品。在分析之前,先对酸性药物进行甲基化处理,然后直接分析咖啡因。此处详细介绍了一种用于分析目标酸性药物和咖啡因的气相色谱-离子阱串联质谱法(IT-MS / MS)。调整了碰撞诱导解离(CID)电压,隔离时间,激发时间,激发存储能级和电子能等参数,以优化仪器的分析性能。优化后,所有目标分析物的仪器检出限为0.5-20 pg /μL,信噪比(S / N)不小于5。结果表明,该方法在10-2000 pg / mu L的范围内具有良好的线性。优化的IT-MS / MS参数与样品前处理步骤的结合使用,可实现方法检测限(MDL)为0.1-1.0分别用于测定地表水,市政污水厂废水以及接收水等样品中的酸性药物和咖啡因的浓度分别为20 ng / L和20 ng / L。 (c)2006 Elsevier B.V.保留所有权利。

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