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胺碘酮在人体中的药代动力学及体内分布

Pharmacokinetics and body distribution of amiodarone in man.

作者信息

Plomp T A, van Rossum J M, Robles de Medina E O, van Lier T, Maes R A

出版信息

Arzneimittelforschung. 1984;34(4):513-20.

PMID:6540111
Abstract

The concentrations of amiodarone (Cordarone) and desethylamiodarone in plasma after single oral and intravenous and long-term oral dosing were determined in seven normal subjects and 106 patients with various cardiac arrhythmias, respectively, using a high-performance liquid chromatographic method. The decline in amiodarone plasma concentration after a single intravenous 400 mg dose was described by a triexponential decay equation, with a mean terminal half-life (t1/2) of 34.5 h. Model independent parameters were calculated from the fits. Mean values for clearance and apparent volume of distribution were 14.7 +/- 7.2 l/h and 376 +/- 372 l. Following single oral doses of 400 mg, amiodarone plasma concentration time data were fitted in a triexponential function. The mean terminal half-life for amiodarone after oral dosage was 31.6 +/- 21.3 h. Amiodarone peak concentrations of 0.37 +/- 0.22 micrograms/ml were attained in 4.8 +/- 1.5 h. The bioavailability of oral amiodarone was only 31 +/- 26%, in part due to first-pass metabolism. Desethylamiodarone , the major metabolite of amiodarone, was present in plasma in very low levels of about 10 ng/ml in several volunteers after single intravenous or oral administration of amiodarone. The mean plasma amiodarone and desethylamiodarone levels in 106 patients, using a mean oral daily maintenance dosage of 440 +/- 253 mg for a mean period of 9.1 months, were 1.85 +/- 1.17 micrograms/ml and 1.35 +/- 0.71 micrograms/ml, respectively. The relationship between the steady state amiodarone and desethylamiodarone plasma concentrations and daily amiodarone maintenance dose in mg in 106 patients was investigated.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用高效液相色谱法,分别测定了7名正常受试者和106例各种心律失常患者单次口服、静脉注射及长期口服胺碘酮(可达龙)后的血浆中胺碘酮和去乙基胺碘酮浓度。静脉注射400mg单次剂量后,胺碘酮血浆浓度的下降可用三指数衰减方程描述,平均终末半衰期(t1/2)为34.5小时。根据拟合结果计算模型独立参数。清除率和表观分布容积的平均值分别为14.7±7.2l/h和376±372l。单次口服400mg后,胺碘酮血浆浓度-时间数据拟合为三指数函数。口服胺碘酮后的平均终末半衰期为31.6±21.3小时。4.8±1.5小时内达到的胺碘酮峰值浓度为0.37±0.22μg/ml。口服胺碘酮的生物利用度仅为31±26%,部分原因是首过代谢。去乙基胺碘酮是胺碘酮的主要代谢产物,在几名志愿者单次静脉或口服胺碘酮后,血浆中其含量极低,约为10ng/ml。106例患者平均口服每日维持剂量为440±253mg,平均服用9.1个月,其血浆中胺碘酮和去乙基胺碘酮的平均水平分别为1.85±1.17μg/ml和1.35±0.71μg/ml。研究了106例患者稳态胺碘酮和去乙基胺碘酮血浆浓度与每日胺碘酮维持剂量(mg)之间的关系。(摘要截断于250字)

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