Ahrer W, Scherwenk E, Buchberger W
Department of Analytical Chemistry, Johannes-Kepler-University Linz, Austria.
J Chromatogr A. 2001 Feb 23;910(1):69-78. doi: 10.1016/s0021-9673(00)01187-0.
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.
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。