Graham D J, Dow R J, Freedman D, Mroszczak E, Ling T
Postgrad Med J. 1984;60 Suppl 4:7-10.
The pharmacokinetics of nicardipine have been studied following oral and intravenous administration in man and the effects of food on nicardipine kinetics investigated. Following intravenous administration of nicardipine as an infusion plasma levels declined in a biphasic manner and plasma clearance values were of the same order as hepatic plasma flow. Following oral administration in the starved state nicardipine was rapidly absorbed but subject to presystemic elimination. Maximal plasma concentrations were achieved typically between 20 minutes and 2 hours after administration. The oral bioavailability of nicardipine determined by reference to a co-administered intravenous radiolabelled dose was found to be non-linearly related to dose. Bioavailability ranged from 15-45% approximately over the dose range 10-40 mg. Administration of nicardipine following a meal reduced the bioavailability of nicardipine.
已对尼卡地平在人体口服和静脉给药后的药代动力学进行了研究,并考察了食物对尼卡地平动力学的影响。静脉输注尼卡地平后,血浆浓度呈双相下降,血浆清除率与肝血浆流量处于同一数量级。在饥饿状态下口服给药后,尼卡地平吸收迅速,但存在首过消除。给药后通常在20分钟至2小时之间达到最大血浆浓度。通过参考同时给予的静脉放射性标记剂量测定的尼卡地平口服生物利用度与剂量呈非线性关系。在10 - 40毫克的剂量范围内,生物利用度约为15% - 45%。餐后服用尼卡地平会降低其生物利用度。