首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >BOSWELLIA PAPYRIFERA RESIN AS MICROENCAPSULATING AGENT FOR CONTROLLED RELEASE OF DICLOFENAC SODIUM: FORMULATION, EVALUATION AND OPTIMIZATION STUDY
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BOSWELLIA PAPYRIFERA RESIN AS MICROENCAPSULATING AGENT FOR CONTROLLED RELEASE OF DICLOFENAC SODIUM: FORMULATION, EVALUATION AND OPTIMIZATION STUDY

机译:乳香乳杆菌树脂作为微胶囊化剂控制双氯芬酸钠的释放:配方,评价和优化研究

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Objective: The present study is aimed to investigate the resin from local olibanum (Boswellia papyrifera) as a wall material for microencapsulation using diclofenac sodium as a model drug. Methods: Microcapsule formulations were prepared by solvent evaporation method with varying polymer to drug ratio, stirring rate, temperature and dispersed phase volumes and their effects on percentage yield, particle size, encapsulation efficiency and release rate were evaluated. Results: The preliminary experiments revealed that the polymer to drug ratio and stirring rate significantly affect both the encapsulation efficiency and release rate while the other factors only affect one of the responses. Therefore, the effects of polymer to drug ratio and stirring rate on the encapsulation efficiency and release rate of the microcapsules were further studied and optimized by central composite design. The optimal conditions were obtained at 3.7:1 polymer to drug ratio and 1200 rpm stirring rate. Under these conditions, the encapsulation efficiency and release rate were 26.45 % and 27.87 h-1/2, respectively. The optimum formulation also provided discrete, spherical and freely flowing microcapsules. The in vitro drug release exhibited minimum burst release with sustained release for 12 h. The kinetic study showed the optimized formulat ion followed Higuchi square root kinetic model with non-Fickian diffusion release mechanism. Conclusion: The results of this study showed that the resin of B. papyrifera could be used as a potential alternative wall material for microencapsulation
机译:目的:本研究旨在研究以双氯芬酸钠为模型药物,将局部乳脂(乳香乳突果)作为壁材料进行微囊化的树脂。方法:采用溶剂蒸发法,通过改变聚合物与药物的比例,搅拌速率,温度和分散相体积,制备微胶囊制剂,并考察其对收率,粒径,包封效率和释放速率的影响。结果:初步实验表明,聚合物与药物的比例和搅拌速率均显着影响包封效率和释放速率,而其他因素仅影响一种响应。因此,通过中心复合设计进一步研究和优化了聚合物与药物的比例和搅拌速率对微胶囊的包封效率和释放速率的影响。聚合物与药物的比例为3.7:1,搅拌速度为1200 rpm,可获得最佳条件。在这些条件下,包封率和释放率分别为26.45%和27.87h-1 / 2。最佳配方还提供了离散的,球形的和自由流动的微胶囊。体外药物释放表现出最小的突释释放,并持续释放12 h。动力学研究表明,优化的离子遵循Higuchi平方根动力学模型,具有非Fickian扩散释放机理。结论:这项研究的结果表明,乳杆菌的树脂可以用作微囊化的潜在替代壁材料。

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