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首页> 外文期刊>Analytical chemistry >Determination of carbamazepine and its metabolites in aqueous samples using liquid chromatography-electrospray tandem mass spectrometry
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Determination of carbamazepine and its metabolites in aqueous samples using liquid chromatography-electrospray tandem mass spectrometry

机译:液相色谱-电喷雾串联质谱法测定水溶液中的卡马西平及其代谢物

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摘要

A quantitative method is described for solid-phase extraction (SPE) followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the simultaneous analysis of carbamazepine and its five metabolites, 10,11-dihydro-10,11-epoxycarbamazepine, 10,11-dihydro-10,11-dihydroxycarbamazepine, 2-hydroxycarbamazepine, 3-hydroxycarbamazepine, and 10,11-dihydro10-hydroxycarbamazepine. An SPE procedure was used to concentrate target compounds from aqueous samples collected from sewage treatment plant (STP) wastewater and surface water. Extracts were analyzed using electro-spray LC-MS/MS with time-scheduled selected reaction monitoring. The recoveries of the analytes were 83.6-102.2% from untreated sewage (influent), 90.6-103.5% from treated sewage (effluent), and 95.7-102.9% from surface water samples. The instrumental detection limits were 0.8-4.8 pg for the analytes. Matrix effects were investigated for the analytes in HPLC-grade water, surface water, and SIT influent and effluent. Ion suppression increased for analytes in order of surface water to STP effluent to STP influent, but no ion suppression was observed for analytes in HPLC-grade water. The developed method was validated by analysis of environmental aqueous samples: STP influent and effluent and surface water. Carbamazepine and all five metabolites were detected in SIT influent and effluent samples. Only carbamazepine and 10,11-dihydro-10,11-dihydroxycarbamazepine were detected in the surface water sample. Notably, 10,11-dihydro-10,11-dihydroxycarbamazepine was detected at similar to3 times higher concentrations than the parent drug, carbamazepine, in all of the aqueous samples. To our knowledge, this is the first report on the simultaneous determination of carbamazepine and its metabolites in environmental samples. [References: 36]
机译:描述了一种定量方法,用于固相萃取(SPE),然后进行液相色谱-串联质谱(LC-MS / MS),用于同时分析卡马西平及其五种代谢物10,11-dihydro-10,11-epoxycarbamazepine ,10,11-二氢-10,11-二羟基卡马西平,2-羟基卡马西平,3-羟基卡马西平和10,11-二氢10-羟基卡马西平。使用SPE程序从污水处理厂(STP)废水和地表水中收集的水性样品中浓缩目标化合物。使用电喷雾LC-MS / MS对萃取物进行分析,并按时间表安排选定的反应监测。未经处理的污水(进水)的分析物回收率为83.6-102.2%,经过处理的污水(出水)的回收率为90.6-103.5%,地表水样品的回收率为95.7-102.9%。分析物的仪器检测限为0.8-4.8 pg。研究了HPLC级水,地表水以及SIT进水和出水中分析物的基质效应。对于分析物,离子抑制作用依从地表水到STP流出物到STP流入物的顺序增加,但是在HPLC级水中,没有观察到离子对分析物的抑制作用。通过分析环境水样:STP进水和出水以及地表水,验证了该方法的有效性。在进水口和出水口样品中检出了卡马西平和所有五种代谢物。在地表水样品中仅检测到卡马西平和10,11-二氢-10,11-二羟基卡马西平。值得注意的是,在所有水性样品中,检出的10,11-二氢-10,11-二羟基卡马西平的浓度比母体药物卡马西平高3倍。据我们所知,这是同时测定环境样品中卡马西平及其代谢物的第一份报告。 [参考:36]

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