4.4 Article

Designing of the fixed-dose gastroretentive bilayer tablet for sustained release of metformin and immediate release of atorvastatin

期刊

DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY
卷 42, 期 2, 页码 340-349

出版社

TAYLOR & FRANCIS LTD
DOI: 10.3109/03639045.2015.1096279

关键词

Ammonium methacrylate copolymer; dissolution test; fixed-dose combination; pharmacokinetic study; polyethylene oxide

资金

  1. Chungcheong institute for regional program evaluation (CIRPE) promotion project of the Ministry of Trade, Industry and Energy (MOTIE), Republic of Korea [800-20130292, R0001833]
  2. Korea Evaluation Institute of Industrial Technology (KEIT) [R0001833] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Patients with type 2 diabetes mellitus have a high risk of cardiovascular disease mainly caused by dyslipidemia. Metformin and atorvastatin are preferentially used to treat type 2 diabetes mellitus and dyslipidemia, respectively. The aim of this study was to develop a once-a-day fixed-dose combination tablet containing metformin and atorvastatin. For this purpose, we designed gastroretentive bilayer tablets consisting of 500mg metformin in a sustained release layer and 10mg atorvastatin in an immediate release layer. In addition, we modified the formulation to maintain a dual release pattern for the kinetically different layers for once-daily dosing. The gastroretentive bilayer tablet was developed using polyethylene oxide as a swellable polymer and ammonium methacrylate copolymer as a granule-coating polymer with minimal use of excipients. In vitro release patterns of metformin and atorvastatin from the developed formulation were similar to those of the reference drugs, Glucophage XR for metformin and Lipitor for atorvastatin, with satisfactory dissolution similarity factor (f(2)) values. The pharmacokinetic study showed the sustained and immediate absorptions of metformin and atorvastatin, respectively, in beagle dogs. The 90% confidence intervals of the ratios of ln values of AUCs of test formulation F3 and respective reference formulations of metformin and atorvastatin were 0.93-1.12 and 0.89-1.17, respectively, compared with their respective reference drugs. This formulation could contribute to improving the compliance and therapeutic outcome of patients with metabolic diseases.

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