Quality by design enabled formulation optimization of rabeprazole sodium mucoadhesive microcapsules for the treatment of gastroesophageal reflux disease

IF 0.3 Q4 PHARMACOLOGY & PHARMACY
S. Swain, Jayanti Panda, M. E. Bhanoji Rao
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引用次数: 0

Abstract

The present research describes the implementation of quality by-design principles for developing the mucoadhesive microcapsules of rabeprazole sodium for treating gastroesophageal reflux disease conditions. In addition, a holistic QbD-based product development strategy was implemented, where the target product profile was defined based on desired product quality of mucoadhesive microcapsules. Based on TPP, the critical quality attributes were identified. The identification of CMAs was carried out with the help of risk assessment and factor screening exercises, which indicated drug-polymer ratio (X1), temperature (X2), and stirring speed (X3) as the influential factors. The mucoadhesive microcapsules of rabeprazole sodium were prepared by a solvent evaporation method, and 33 Box-Behnken optimization design was used for the optimization of the selected factors, and mucoadhesive microcapsules formulations were evaluated for particle size (µm), drug entrapment efficiency (%), mucoadhesion (%), and in vitro drug release (Q18h) in percentage characteristics. Mathematical data analysis was performed to fit the two-factor interaction model, and optimized mucoadhesive microcapsules formulation was selected. The optimized mucoadhesive microcapsules indicated desired formulation characteristics with smaller particle size, good entrapment efficiency, better mucoadhesion, and sustained drug release characteristics. In a nutshell, the studies vouch for the successful development of mucoadhesive microcapsules for oral delivery of rabeprazole sodium which could be used to manage gastroesophageal reflux disease condition.
雷贝拉唑钠粘附微胶囊治疗胃食管反流病的设计质量配方优化
本研究描述了通过设计原则开发用于治疗胃食管反流疾病的雷贝拉唑钠粘膜粘附微胶囊的质量实施。此外,实施了基于QbD的整体产品开发策略,其中基于粘膜粘合剂微胶囊的期望产品质量来定义目标产品概况。基于TPP,确定了关键质量属性。CMA的鉴定是在风险评估和因素筛选的帮助下进行的,其中药物聚合物比例(X1)、温度(X2)和搅拌速度(X3)是影响因素。采用溶剂蒸发法制备了雷贝拉唑钠的粘膜粘附微胶囊,并采用33 Box-Behnken优化设计对所选因素进行了优化,并以百分比特性评估了粘膜粘附微丸制剂的粒径(µm)、药物包封率(%)、粘粘性(%)和体外药物释放(Q18h)。通过数学数据分析,拟合双因素相互作用模型,筛选出最佳的粘黏微胶囊配方。优化的粘膜粘附微胶囊显示出所需的制剂特性,具有更小的颗粒尺寸、良好的包封效率、更好的粘膜粘附性和持续的药物释放特性。简言之,这些研究证明了用于口服雷贝拉唑钠的粘膜粘附微胶囊的成功开发,该微胶囊可用于治疗胃食管反流疾病。
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来源期刊
Current Drug Therapy
Current Drug Therapy PHARMACOLOGY & PHARMACY-
CiteScore
1.30
自引率
0.00%
发文量
50
期刊介绍: Current Drug Therapy publishes frontier reviews of high quality on all the latest advances in drug therapy covering: new and existing drugs, therapies and medical devices. The journal is essential reading for all researchers and clinicians involved in drug therapy.
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