Vens-Cappell B, Berndt P, Hilgenstock C, Kühle K, Reifferscheid I, Schütt S, Bührens K G
McKnight Laboratories GmbH, Hamburg.
Arzneimittelforschung. 1993 Mar;43(3):351-6.
The pharmacokinetic profile of a 300 mg immediate release formulation (A) was compared to a 400 mg sustained release formulation (B) of the lipid lowering drug bezafibrate (CAS 41859-67-0). Preparation A was applied twice a day whereas B was applied once a day in the evening. The means of Cmax (12.5 micrograms/ml) and AUC (66.8 micrograms/ml.h) for preparation A were considerably higher than for B (Cmax: 6.6 micrograms/ml, AUC: 39.8 micrograms/ml.h), whereas no differences were found regarding Tcav (A: 8.9 h, B: 8.3 h) and PTF (A: 4.6, B; 4.1). An AUC ratio for A/B of 119% (CI90%: 108-132%) was determined after dose correction. For A an AUC/AUEC ratio of 110% was found when comparing multiple versus single-dose application, whereas this ratio with 136% appeared to be considerably higher for B. Slight chronopharmacological effects were found for preparation A, which was applied twice a day in the evening and in the morning. During night-time the AUC was (insignificantly) 12% higher than during day-time, whereas the apparent elimination halflife time was 40% longer at night (p < 0.025), which corresponded to an extended tmax of median 3 h during night-time as compared to 1.75 h at day-time.
将降脂药物苯扎贝特(CAS 41859-67-0)的300毫克速释制剂(A)的药代动力学特征与400毫克缓释制剂(B)进行了比较。制剂A每天服用两次,而B每天晚上服用一次。制剂A的Cmax(12.5微克/毫升)和AUC(66.8微克/毫升·小时)均值显著高于B(Cmax:6.6微克/毫升,AUC:39.8微克/毫升·小时),而在平均驻留时间(A:8.9小时,B:8.3小时)和峰谷波动系数(A:4.6,B:4.1)方面未发现差异。剂量校正后,A/B的AUC比值为119%(90%置信区间:108-132%)。与单剂量应用相比,A的AUC/AUEC比值为110%,而B的该比值为136%,明显更高。对于每天早晚各服用一次的制剂A,发现了轻微的时辰药理学效应。夜间的AUC比白天(无显著差异)高12%,而表观消除半衰期在夜间长40%(p<0.025),这对应于夜间的tmax中位数延长3小时,而白天为1.75小时。