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首页> 外文期刊>American Journal of PharmTech Research >Design and Evaluation of Sodium Alginate Based Microspheres Loaded With Misoprostal
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Design and Evaluation of Sodium Alginate Based Microspheres Loaded With Misoprostal

机译:米索前列醇负载海藻酸钠微球的设计与评价

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ABSTRACT In the present investigation efforts were made to develop Misoprostal loaded microspheres to obtain a desirable drug release profile by Ionic gelation method using hydrophilic polymers and cross linking agent to decrease the gastric irritation and to enhance the drug penetration. Microspheres were prepared by using sodium alginate and calcium chloride in different ratios.  All the microspheres were evaluated for particle size, percentage yield, drug entrapment efficiency, stability studies and for in vitro release kinetics and found to be within the limits. Among all the formulations S7 was selected as optimized formulation based on the physico chemical properties and drug release studies. In vitro drug release study of formulation S7 showed 97.17% drug release up to 12h in a controlled manner, which is essential for an anti ulcer therapy. The innovator Misoprostal marketed product shows the drug release of 95.23 in 1 h. The drug release of optimized formulation S7 followed zero order release and Higuchi kinetics indicating diffusion controlled drug release. FT- IR study showed no drug excipient interaction takes place. Keywords: Misoprostol, sodium alginate, microspheres, scanning electron microscopy, release order kinetics.
机译:摘要在目前的研究中,人们进行了努力,开发了使用Misoprostal的微球,通过使用亲水性聚合物和交联剂的离子凝胶法,通过降低凝胶对胃的刺激和增强药物渗透性,获得了理想的药物释放曲线。通过使用不同比例的藻酸钠和氯化钙制备微球。对所有微球的粒径,百分收率,药物截留效率,稳定性研究和体外释放动力学进行了评估,发现均在极限范围内。在所有制剂中,根据理化性质和药物释放研究,选择S7作为优化制剂。制剂S7的体外药物释放研究表明,药物以受控方式释放达12小时的97.17%,这对于抗溃疡治疗至关重要。 Misoprostal市售创新产品在1小时内显示95.23的药物释放。优化制剂S7的药物释放遵循零级释放和Higuchi动力学,表明扩散控制药物释放。 FT-IR研究表明没有药物赋形剂相互作用。关键词:米索前列醇海藻酸钠微球扫描电镜释放顺序动力学

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