Bioavailability of gliclazide from some formulation tablets

被引:21
作者
Glówka, FK
Hermann, TW
Zabel, M
机构
[1] K Marcinkowski Univ Med Sci, Dept Phys Chem, PL-60781 Poznan, Poland
[2] Univ Med Sci, Dept Histol & Embriol, PL-50368 Wroclaw, Poland
关键词
gliclazide; bioavailabilty; tablets; volunteers; serum; release in vitro; hypoglycemic effect; humans;
D O I
10.1016/S0378-5173(98)00167-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabezid, from Jelfa, and diabrezide, from Molteni, tablets are bioequivalent as well as producing pharmacokinetic parameters typical for classic gliclazide oral formulations (C-max = 3.4-4.1 mg l(-1), t(max) = 3.5-4.6 h, t(0.5) = 5.2-6.5 h). In contrast, diaprel tablets, from Servier, seem to be a sustained release formulation and is not bioequivalent to the above tablets. It produces a long tablet disintegration time (58 min) and the dissolution of gliclazide in 0.1 mol l(-1) HCl (9.04 mg l(-1) (11.3%) at 4 h and 37 degrees C) as well as in serum C-max (0.7 mg l(-1)) are poor. In contrast with the Jelfa tablets, the Servier tablets do not demonstrate any hypoglycemic effect in healthy volunteers. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
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页码:71 / 77
页数:7
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