Vargas M G, Havel J, Patocka J
Department of Analytical Chemistry, Faculty of Sciences, Masaryk University, Brno, Czech Republic.
J Chromatogr A. 1998 Apr 3;802(1):121-8. doi: 10.1016/s0021-9673(97)01117-5.
A new capillary zone electrophoresis (CZE) method for the determination of tacrine (THA), 7-methoxytacrine (7-MTHA) and their basic metabolites (THAm, 7-MTHAm) in pharmaceutical and biological samples (urine and serum) was developed. Separation of all compounds by CZE was carried out using a 46.6 cm untreated fused-silica capillary applying 20 kV separation voltage using 50 mM phosphate buffer of pH 2.8 for THA and THAm and of pH 7.8 for 7-MTHA and 7-MTHAm as background electrolyte (BGE). Detection was carried out at 240 nm (THA and THAm) and 248 nm (7-MTHA and 7-MTHAm). THA and THAm were separated in less than 4 min while 7-MTHA and 7-MTHAm were separated in less than 7 min. The detection limits (SIN = 3) obtained were 3 ppb for THA and 4 ppb for 7-MTHA in aqueous solutions; 50 ppb for THA and 47 ppb for 7-MTHA for the determination in urine (diluted 1:10); 52 ppb for THA and 56 ppb for 7-MTHA, in deproteinized serum samples. The methods are suitable for therapeutic drug monitoring of the drugs.
建立了一种新的毛细管区带电泳(CZE)方法,用于测定药物和生物样品(尿液和血清)中的他克林(THA)、7-甲氧基他克林(7-MTHA)及其碱性代谢产物(THAm、7-MTHAm)。采用46.6 cm未处理的熔融石英毛细管进行CZE分离,以50 mM pH 2.8的磷酸盐缓冲液用于THA和THAm、pH 7.8的磷酸盐缓冲液用于7-MTHA和7-MTHAm作为背景电解质(BGE),施加20 kV分离电压。检测在240 nm(THA和THAm)和248 nm(7-MTHA和7-MTHAm)处进行。THA和THAm在不到4分钟内分离,而7-MTHA和7-MTHAm在不到7分钟内分离。在水溶液中获得的检测限(S/N = 3),THA为3 ppb,7-MTHA为4 ppb;在尿液(稀释1:10)中测定时,THA为50 ppb,7-MTHA为47 ppb;在脱蛋白血清样品中,THA为52 ppb,7-MTHA为56 ppb。这些方法适用于这些药物的治疗药物监测。