Ziegler V E, Biggs J T, Ardekani A B, Rosen S H
J Clin Pharmacol. 1978 Oct;18(10):462-7. doi: 10.1002/j.1552-4604.1978.tb01572.x.
The clinical pharmacokinetics of amitriptyline were studied in four volunteers after the oral administration of 75 mg. Peak amitriptyline plasma concentrations ranged from 10.8 to 43.7 ng/ml. The disappearance was biphasic and followed first-order kinetics. The mean elimination half-life was 36.1 hours. The mean estimated first-pass metabolism of amitriptyline was 60 per cent. Significant quantities of the metabolite, nortriptyline, were produced although peak concentrations ranged from only 5.9 to 12.3 ng/ml. The relationship between these findings to clinical practice and earlier reports is discussed.
在4名志愿者口服75毫克阿米替林后,对其临床药代动力学进行了研究。阿米替林的血浆峰浓度在10.8至43.7纳克/毫升之间。其消除呈双相,符合一级动力学。平均消除半衰期为36.1小时。阿米替林的平均首过代谢估计为60%。尽管代谢物去甲替林的峰浓度仅在5.9至12.3纳克/毫升之间,但仍产生了大量该代谢物。讨论了这些研究结果与临床实践及早期报告之间的关系。