Anavekar S N, Howes L G, Jarrott B, Syrjanen M, Conway E L, Louis W J
University of Melbourne, Department of Medicine, Heidelberg, Victoria, Australia.
J Clin Pharmacol. 1989 Apr;29(4):321-6. doi: 10.1002/j.1552-4604.1989.tb03335.x.
Using a sensitive and specific radioimmunoassay the pharmacokinetic disposition of clonidine was determined in hypertensive patients after a single dose and then after 5, 28 and 56 days of chronic dosing with 75 micrograms bd. Following a single dose of clonidine maximal plasma concentrations of 0.34 +/- 0.06 ng/ml were achieved after 3.6 +/- 1.2 hours. After 5 days of repetitive dosing the maximal concentration was significantly higher, 0.66 +/- 0.06 ng/ml and remained so throughout chronic therapy (P = 0.018). The AUC, Tmax and T1/2 did not differ significantly between the acute dose and the chronic dosing pharmacokinetic studies. Clonidine also produced a significant fall in blood pressure. Supine diastolic blood pressure fell from 106 +/- 5 mmHg predose to 99 +/- 6 mmHg 2 hours after the first dose (P less than 0.05). The corresponding values after cyclopenthiazide alone were 108 +/- 8 and 105 +/- 8 mmHg (P = 0.13). Similar falls in blood pressure were produced during chronic therapy.
采用灵敏且特异的放射免疫分析法,对高血压患者单次给药后以及连续5天、28天和56天每日两次服用75微克可乐定后的药代动力学情况进行了测定。单次服用可乐定后,在3.6±1.2小时达到最大血浆浓度0.34±0.06纳克/毫升。重复给药5天后,最大浓度显著升高,为0.66±0.06纳克/毫升,且在整个长期治疗过程中均保持如此(P = 0.018)。急性给药和长期给药的药代动力学研究中,曲线下面积(AUC)、达峰时间(Tmax)和半衰期(T1/2)无显著差异。可乐定还使血压显著下降。首次给药后2小时,仰卧位舒张压从给药前的106±5毫米汞柱降至99±6毫米汞柱(P<0.05)。单独使用环戊噻嗪后的相应值分别为108±8和105±8毫米汞柱(P = 0.13)。长期治疗期间血压也出现了类似下降。