FORMULATION AND EVALUATION OF MODIFIED RELEASE TRI-LAYERED TABLET USING A FIXED DOSE COMBINATION OF METFORMIN HCL AND VILDAGLIPTIN

A. Jain, Geeta K Patel
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Abstract

The aim of present investigation is to formulate the tri-layered tablet of an Anti-Hyperglycaemic drug comprising Metformin HCl as sustained release layer and Vildagliptin as an immediate release layer in a fixed dose combination along with a fast dissolving intermediate layer or barrier layer in between the two layers just like a sandwich. Vildagliptin is well-known for its instability in presence of Metformin HCl. Hence, Vildagliptin degrades in formulation of single unit dosage form. The in vitro release layer of Metformin HCl was prepared using combination of sustained release polymer HPMC K100M & HPMC K4M and binder used in formulation is Povidone K90 which was prolonged up to 10 - 12 hours. The In-vitro release of Vildagliptin is rapid from tablet and showed highest drug release of more than 90% in 30 Minutes. Final formulation was tested for accelerated stability study. Intermediate barrier layer was optimised using Lactose Monohydrate and Microcrystalline cellulose as a diluents and Croscarmellose sodium as a disintegrant. The disintegration time of tablet into two halves for final formulation was 51 seconds. Combination of lactose monohydrate and microcrystalline cellulose as well as thickness of the intermediate layer was found important to achieve quick disintegration.
盐酸二甲双胍与维格列汀固定剂量联合缓释三层片的研制与评价
以盐酸二甲双胍为缓释层,维格列汀为速释层的三层抗高血糖药物为固定剂量组合,并在两层之间形成快速溶解的中间层或屏障层。维格列汀因其在盐酸二甲双胍中不稳定而闻名。因此,维格列汀在单单位剂型制剂中降解。采用HPMC K100M和HPMC K4M缓释聚合物,结合剂为聚维酮K90制备盐酸二甲双胍体外释放层,缓释时间为10 ~ 12小时。维格列汀的体外释放速度快,30分钟内释药率最高可达90%以上。对最终配方进行了加速稳定性研究。以一水乳糖和微晶纤维素为稀释剂,交联纤维素钠为崩解剂,优化中间屏障层。片剂分两半崩解时间为51秒。发现一水乳糖和微晶纤维素的结合以及中间层的厚度对实现快速分解很重要。
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