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机构地区:[1]衡阳市中心医院药剂科,湖南衡阳421001 [2]南华大学附属第一医院,湖南衡阳421001 [3]湘雅医学院附属第三医院,湖南长沙410078
出 处:《湖南环境生物职业技术学院学报》2009年第4期13-17,共5页JOurnal of Hunan Environment Biological Polytechnic
摘 要:目的研究吗替麦考酚酯胶囊在健康人体内的药动学和相对生物利用度,进行生物等效性评价.方法18名男性健康志愿者双周期随机交叉单次口服吗替麦考酚酯胶囊1 g,服药间隔为l周,采用高效液相色谱法测定血浆中麦考酚酸浓度.结果两种制剂主要药动学参数无显著性差异,参比和受试的Cm ax分别为37.91±10.38和37.70±7.75 mg/L;tm ax分别为0.52±0.38 h和0.50±0.25 h;tl/2分别为16.37±9.90 h和13.85±8.83 h;AUC0→24分别为每升62.00±10.12 mg/h和每升60.10±10.21 mg/h.吗替麦考酚酯胶囊的相对生物利用度为97.59±12.24%.结论2种制剂具有生物等效性.图4,表4。Objective To investigate the pharmacokinetics and relative bioavailability of mycophenolate mofetil capsules in healthy volunteers, and to evaluate its bioequivalence. Methods A single oral dose of 1 g of two kinds of mycophenolate mofetil capsules was administered by randomized crossover way in 18 male healthy vol- unteers, and the plasma concentrations of mycophenolic acid were determined by high performance liquid chromatography (HPLC). Result The main pharmacokinetic parameters have no significant differences of be- tween two kinds of preparations. The pharmacokinetic parameters of reference preparation and tested prepara- tions were as follows :Cmax,= ( 37.91 ± 10.38 ), ( 37.70 ±7.75 )mg/L; tmax(0.52 ±0.38)h , (0.50 ±0.25) h ;t1/2 ( 16.37± 9.90) h, ( 13.85 ± 8.83 ) h; AUC0→24 (62.00 ± 10.12) mg/h · L, (60.10 ± 10.21 ) mg/h · L. The relative bioavailability of the tested preparation was (97.59 ± 12.24) %. Conclusion The reference preparation and the tested preparation were bioequivalent. 4figs. , 4tabs. , 5refs.
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