Matrix tablets for sustained release of repaglinide: Preparation, pharmacokinetics and hypoglycemic activity in beagle dogs

被引:24
|
作者
He, Wei [1 ]
Wu, Mengmeng [1 ]
Huang, Shiqing [2 ]
Yin, Lifang [1 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Third Peoples Hosp Chengdu, Chengdu 610031, Peoples R China
关键词
Repaglinide; Sustained release tablets; Pharmacokinetics; In vitro/in vivo correlation; Hypoglycemic effect; DRUG-RELEASE; METFORMIN HYDROCHLORIDE; MICROENVIRONMENTAL PH; BIPHASIC RELEASE; BASIC DRUG; IN-VITRO; INDOMETHACIN; PARAMETERS; ALGINATE; DELIVERY;
D O I
10.1016/j.ijpharm.2014.11.059
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Repaglinide (RG) is an efficient antihyperglycemic drug; however, due to its short half-life, patients are required to take the marketed products several times a day, which compromises the therapeutic effects. The present study was conducted to develop a hydrophilic sustained release matrix tablet for RG with the aims of prolonging its action time, reducing the required administration times and side effects and improving patient adherence. The matrix tablets were fabricated by a direct compression method, the optimized formulation for which was obtained by screening the factors that affected the drug release. Moreover, studies of the pharmacokinetics and hypoglycemic activity as measured by glucose assay kits were performed in dogs. Sustained drug releases profiles over 10 h and a reduced influence of medium pHs on release were achieved with the optimized formulation; moreover, the in vivo performance of extended release formulation was also examined, and better absorption, a one-fold decrease in C-max a two-fold increase of T-max and a prolonged hypoglycemic effect compared to the marketed product were observed. In conclusion, sustained RG release and prolonged action were observed with present matrix tablets, which therefore provide a promising formulation for T2D patients who require long-term treatment. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:297 / 307
页数:11
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