Site-specific oral controlled release metformin tablets - development, in vitro, ex vivo and in vivo evaluation

V. Prakya, Kusumdevi Vemula, K. Devi, S. Sonti
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引用次数: 1

Abstract

Oral absorption of metformin is confined to the upper part of intestine posing problems in the formulation of extended release tablets. Therefore, the objective of the present study was to develop controlled-release mucoadhesive core tablets and confine the tablets to the specific site in the gastrointestinal tract. A projective coat protects the core tablets from mucoadhesion till the targeted site is reached. Once the tablet reaches the specific site, the coat dissolves exposing the core tablet for mucoadhesion. In vitro coat intactness test and ex vivo tablet bioadhesion test confirmed that the tablets were targeted and contained in the upper intestine. Further, the pharmacokinetic parameters obtained for metformin from the site-specific coated formulation were better (P<0.05) than that of the non-site-specific uncoated formulation in the in vivo studies. Standardized formulation was stable during the stability studies conducted as per ICH Q1C guidelines.
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部位特异性口服控释片二甲双胍-开发,体外,离体和体内评价
二甲双胍的口服吸收局限于肠道上部,给缓释片的配方带来了问题。因此,本研究的目的是开发控释黏附核心片,并将其限制在胃肠道的特定部位。投射涂层保护核心片免受黏液粘附,直到到达目标部位。一旦片剂到达特定部位,涂层就会溶解,暴露出核心片剂的黏附。体外被膜完整性试验和离体生物黏附试验证实该片剂在上肠内具有靶向性。此外,在体内研究中,位点特异性包衣制剂获得的二甲双胍药动学参数优于非位点特异性包衣制剂(P<0.05)。在按照ICH Q1C指南进行的稳定性研究中,标准化制剂是稳定的。
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