el Allaf D, Carlier J, Dressé A
Int J Clin Pharmacol Res. 1986;6(4):303-7.
Mexiletine (1-methyl-2-(2, 6-xylyloxy)ethylamine hydrochloride) is an antiarrhythmic drug eliminated primarily by hepatic metabolism. The influence of age on the plasma pharmacokinetics of mexiletine was assessed in seven young and ten elderly healthy subjects. Mexiletine (50 mg) was administered orally three times daily for 10 days. The use of low doses of mexiletine was possible owing to the development of a new fluorescence high performance liquid chromatography method with a limit of sensitivity lower than 20 ng/ml. No differences in the pharmacokinetic parameters of mexiletine related to age were observed. At steady-state plasma concentrations were 0.121 +/- 0.033 microgram-ml in the young volunteers, and 0.135 +/- 0.150 microgram/ml in the older subjects. The elimination t 1/2 was 11.4 +/- 1.78 h in the young subjects and 10.48 +/- 3.06 h in the elderly. The data provide no justification for lowering the recommended dose of mexiletine for older patients.
美西律(盐酸1-甲基-2-(2,6-二甲苯氧基)乙胺)是一种主要通过肝脏代谢消除的抗心律失常药物。在7名年轻和10名老年健康受试者中评估了年龄对美西律血浆药代动力学的影响。美西律(50毫克)每日口服3次,共服用10天。由于开发了一种灵敏度极限低于20纳克/毫升的新型荧光高效液相色谱法,因此可以使用低剂量的美西律。未观察到美西律药代动力学参数与年龄相关的差异。年轻志愿者的稳态血浆浓度为0.121±0.033微克/毫升,老年受试者为0.135±0.150微克/毫升。年轻受试者的消除半衰期为11.4±1.78小时,老年受试者为10.48±3.06小时。这些数据没有理由降低老年患者美西律的推荐剂量。