Mercolini Laura, Bugamelli Francesca, Kenndler Ernst, Boncompagni Giancarlo, Franchini Livia, Raggi Maria Augusta
Faculty of Pharmacy, Department of Pharmaceutical Sciences, Alma Mater Studiorum--University of Bologna, Via Belmeloro 6, I-40126 Bologna, Italy.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Feb 1;846(1-2):273-80. doi: 10.1016/j.jchromb.2006.09.019. Epub 2006 Oct 12.
A HPLC method with UV detection has been developed for the simultaneous determination of levomepromazine, clozapine and their main metabolites: N-desmethyl-levomepromazine, levomepromazine sulphoxide, O-desmethyl-levomepromazine, N-desmethylclozapine and clozapine N-oxide. The analytes were separated on a C8 reversed-phase column using a mobile phase composed of acetonitrile and a pH 2.0, 34 mM phosphate buffer containing 0.3% triethylamine (29:71, v/v). Loxapine was used as the internal standard. A reliable biological sample pre-treatment procedure by means of solid-phase extraction on C1 cartridges was implemented, which allows to obtain good extraction yields (>91%) for all analytes and appropriate sample purification from endogenous interference. The method was validated in terms of extraction yield, precision and accuracy. These assays gave RSD% values for precision always lower than 4.9% and mean accuracy values higher than 92%. The method is suitable for the therapeutic drug monitoring (TDM) of patients undergoing polypharmacy with levomepromazine and clozapine.
已开发出一种采用紫外检测的高效液相色谱法,用于同时测定左美丙嗪、氯氮平及其主要代谢物:N-去甲基左美丙嗪、左美丙嗪亚砜、O-去甲基左美丙嗪、N-去甲基氯氮平和氯氮平N-氧化物。分析物在C8反相柱上进行分离,流动相由乙腈和pH值为2.0、含有0.3%三乙胺的34 mM磷酸盐缓冲液组成(29:71,v/v)。洛沙平用作内标。实施了一种通过C1小柱进行固相萃取的可靠生物样品预处理程序,该程序可使所有分析物获得良好的萃取回收率(>91%),并能有效去除内源性干扰物对样品的污染。该方法在萃取回收率、精密度和准确度方面进行了验证。这些测定的精密度RSD%值始终低于4.9%(相对标准偏差),平均准确度值高于92%。该方法适用于接受左美丙嗪和氯氮平联合用药治疗患者的治疗药物监测(TDM)。