Vens-Cappell B, Hilgenstock C, Gellert M, Kühle K, Reifferscheid I, Winckler P, Bührens K G
McKnight Laboratories GmbH, Hamburg.
Arzneimittelforschung. 1993 Mar;43(3):346-50.
Comparison of the Pharmacokinetic Profiles of a Quick and a Sustained Release Bezafibrate Formulation/1st Communication: Single-dose application The hypolipaemic agent bezafibrate (CAS 41859-67-0) is available as immediate and sustained release formulation. The pharmacokinetic profile of an immediate release 300 mg dragee (A) was compared in a two-way cross-over design to that of a 400 mg sustained release dragee (B). Neglecting the dose difference, the AUEC of A (28.8 micrograms/ml.h) was equal to that of B (27.6 micrograms/ml.h), whereas the bioavailability of A appeared to be higher than that of B when AUEC was corrected for dose (AUEC ratio = 137%). Regarding Cmax and tmax, both formulations exhibited the expected differences.
速释和缓释非诺贝特制剂药代动力学特征的比较/首次通讯:单剂量应用 降血脂药非诺贝特(CAS 41859-67-0)有速释和缓释制剂。采用双向交叉设计比较了300 mg速释糖衣丸(A)与400 mg缓释糖衣丸(B)的药代动力学特征。忽略剂量差异,A的曲线下浓度时间(AUEC,28.8微克/ml·小时)与B的(27.6微克/ml·小时)相等,而当根据剂量校正AUEC时(AUEC比值 = 137%),A的生物利用度似乎高于B。关于最大血药浓度(Cmax)和达峰时间(tmax),两种制剂均表现出预期差异。