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Effects of Formulation and Process Variables on Gastroretentive Floating Tablets with A High-Dose Soluble Drug and Experimental Design Approach

机译:配方和工艺变量对高剂量可溶性药物胃肠滞留漂浮片的影响及实验设计方法

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摘要

To develop sustained release gastro-retentive effervescent floating tablets (EFT), a quality-based experimental design approach was utilized during the composing of a hydrophilic matrix loaded with a high amount of a highly water-soluble model drug, metformin HCl. Effects of the amount of polyethylene oxide WSR 303 (PEO), sodium bicarbonate, and tablet compression force were used as independent variables. Various times required to release the drug, tablet tensile strength, floating lag time, tablet ejection force, and tablet porosity, were selected as the responses. Polymer screening showed that PEO had the highest gel strength among the various tested polymers. Sodium bicarbonate had the most significant effect on the release rate and floating lag time by retarding the rate from the hydrophilic matrices, whilst tablet compression force and PEO exerted the greatest influence on tablet properties (p < 0.0001). The design space was built in accordance with the drug release profiles, tensile strength, and floating lag time, following failure probability analysis using Monte Carlo simulations. The kinetic modeling revealed that the release mechanism was best described by the Korsmeyer-Peppas model. Overall, the current study provided a perspective on the systematic approach of gastro-retentive EFT, loaded with highly water-soluble drugs by applying quality by design concepts.
机译:为了开发持续释放的胃滞留性泡腾片(EFT),在组成载有大量高度水溶性模型药物盐酸二甲双胍的亲水性基质的过程中,采用了基于质量的实验设计方法。聚环氧乙烷WSR 303(PEO)量,碳酸氢钠和片剂压缩力的影响用作自变量。选择释放药物所需的各种时间,片剂的拉伸强度,漂浮滞后时间,片剂的弹射力和片剂的孔隙率作为响应。聚合物筛选表明,PEO在各种测试聚合物中具有最高的凝胶强度。碳酸氢钠通过抑制亲水基体的释放速率,对释放速率和漂浮滞后时间具有最显着的影响,而片剂的压缩力和PEO对片剂的性能影响最大(p <0.0001)。设计空间是根据药物释放曲线,抗张强度和浮动滞后时间建立的,随后使用蒙特卡洛模拟对失效概率进行了分析。动力学模型表明,释放机理最好用Korsmeyer-Peppas模型来描述。总体而言,当前的研究通过应用设计理念的质量,提供了一种胃滞留性EFT的系统方法的观点,该方法富含水溶性药物。

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