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液相色谱或毛细管电泳与电喷雾质谱联用测定水中的药物残留。

Determination of drug residues in water by the combination of liquid chromatography or capillary electrophoresis with electrospray mass spectrometry.

作者信息

Ahrer W, Scherwenk E, Buchberger W

机构信息

Department of Analytical Chemistry, Johannes-Kepler-University Linz, Austria.

出版信息

J Chromatogr A. 2001 Feb 23;910(1):69-78. doi: 10.1016/s0021-9673(00)01187-0.

Abstract

Methods for the determination of drug residues in water have been developed based on the combination of liquid chromatography (LC) or capillary electrophoresis (CE) with mass spectrometry (MS). For HPLC-MS two types of interfaces (pneumatically assisted electrospray ionization interface or an atmospheric pressure chemical ionization interface, respectively) were employed and compared in terms of detection limits. 2 mM Ammonium acetate at pH 5.5 and a methanol gradient was used for the HPLC-MS allowing the separation of a number of drugs such as paracetamol, clofibric acid, penicillin V, naproxen, bezafibrate, carbamazepine, diclofenac, ibuprofen and mefenamic acid. A 20 mM ammonium acetate solution, pH 5.1 was employed for the separation of clofibric acid, naproxen, bezafibrate, diclofenac, ibuprofen and mefenamic acid by CE-MS. Sample pretreatment was performed by solid-phase extraction (SPE) for HPLC-MS or by a combination of liquid-liquid extraction and SPE for CE-MS. The applicability of both the HPLC-MS and CE-MS method was demonstrated for several river water samples.

摘要

基于液相色谱(LC)或毛细管电泳(CE)与质谱(MS)联用,已开发出测定水中药物残留的方法。对于高效液相色谱-质谱联用(HPLC-MS),分别采用了两种类型的接口(气动辅助电喷雾电离接口或大气压化学电离接口),并就检测限进行了比较。在HPLC-MS中,使用pH值为5.5的2 mM醋酸铵和甲醇梯度,可分离多种药物,如对乙酰氨基酚、氯贝酸、青霉素V、萘普生、苯扎贝特、卡马西平、双氯芬酸、布洛芬和甲芬那酸。在CE-MS中,使用pH值为5.1的20 mM醋酸铵溶液来分离氯贝酸、萘普生、苯扎贝特、双氯芬酸、布洛芬和甲芬那酸。对于HPLC-MS,通过固相萃取(SPE)进行样品预处理;对于CE-MS,则通过液液萃取和SPE相结合的方式进行样品预处理。HPLC-MS和CE-MS方法对多个河水样品的适用性均得到了验证。

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