Ulrich S, Isensee T, Pester U
Institute of Clinical Pharmacology, University Hospital, Otto-von-Guericke University, Magdeburg, Germany.
J Chromatogr B Biomed Appl. 1996 Oct 11;685(1):81-9. doi: 10.1016/0378-4347(96)00156-9.
A method for the simultaneous quantification of the antidepressant drug amitriptyline, its demethylated metabolite nortriptyline and four hydroxy metabolites (E-10-hydroxyamitriptyline, Z-10-hydroxyamitriptyline, E-10-hydroxynortriptyline, Z-10-hydroxynortriptyline) in human serum or plasma has been developed. The method is based on a three-step liquid-liquid extraction followed by gas-liquid chromatography (split-splitless injection, HP-5, 25 m x 0.2 mm I.D., 0.33 microns capillary) with nitrogen-phosphorus-selective detection (GLC-NPD). The limits of detection are 1.5 ng/ml for amitriptyline, nortriptyline, E-10-hydroxyamitriptyline and Z-10-hydroxyamitriptyline and 3 ng/ml for E-10-hydroxynortiptyline and Z-10-hydroxynortriptyline. The within-day and between-day precision is between 6 and 15% at three concentrations (low, moderate and high) for amitriptyline, nortriptyline and E-10-hydroxy metabolites. At low concentrations of 10 ng/ml, the precision of the assay of the Z-10-hydroxy metabolites has been found to be up to 19%. Accuracy is between 91 and 115% for all analytes. The performance of the assay of the hydroxy metabolites is mainly determined by the cleanness and the deactivation of the quartz insert of the injector port. Therefore, every day a freshly cleaned and deactivated insert was used.
已开发出一种同时定量测定人血清或血浆中抗抑郁药阿米替林、其去甲基代谢物去甲替林以及四种羟基代谢物(E-10-羟基阿米替林、Z-10-羟基阿米替林、E-10-羟基去甲替林、Z-10-羟基去甲替林)的方法。该方法基于三步液-液萃取,随后进行气-液色谱分析(分流/不分流进样,HP-5,25 m×0.2 mm内径,0.33微米毛细管),采用氮磷选择性检测(GLC-NPD)。阿米替林、去甲替林、E-10-羟基阿米替林和Z-10-羟基阿米替林的检测限为1.5 ng/ml,E-10-羟基去甲替林和Z-10-羟基去甲替林的检测限为3 ng/ml。阿米替林、去甲替林和E-10-羟基代谢物在三个浓度(低、中、高)下的日内和日间精密度在6%至15%之间。在10 ng/ml的低浓度下,发现Z-10-羟基代谢物测定的精密度高达19%。所有分析物的准确度在91%至115%之间。羟基代谢物测定的性能主要取决于进样口石英衬管的清洁度和去活性。因此,每天都使用新清洁和去活性的衬管。