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使用黏液制备用于治疗类风湿性关节炎的脂质体凝胶系统的研发与特性研究

Development and Characterization of Niosomal Gel System using mucilage for the treatment of Rheumatoid Arthritis.

作者信息

Bhardwaj Snigdha, Bhatia Sonam

机构信息

Meerut Institute of Engineering and Technology, Meerut (250005), Uttar Pradesh, India.

Department of Pharmaceutical Science, Shalom Institute of Health and Allied Sciences, SHUATS, Prayagraj (211007), Uttar Pradesh, India.

出版信息

Iran J Pharm Res. 2020 Summer;19(3):465-482. doi: 10.22037/ijpr.2020.112887.14003.

Abstract

Niosomes structural framework comprises of non-ionic surfactant-based microscopic lamellar structures which carries the potential to sustain the effect of drug from its delivery system. In present work, the attempt was made to identify the effect of different ingredients such as effect of Tweens and natural mucilage of on the performance of developed niosomal gel formulations in order to prolong the duration of action of drug and to minimize its side effects of topical conventional drug administration. All Ibuprofen loaded niosomes formulationswere prepared by ether injection method; using cetosteryl alcohol with different variants of Tweens and Spans. Various evaluation parameters were performed to confirm niosome formation. Further, the niosomes were incorporated into gel system and evaluated for i permeability study () on excised rat skin by membrane diffusion method and study by carrageenan induced rat paw edema model. The best selected niosome formulation F9 gave no sedimentation, layer separation and unchanged particle shapes and thus selected for gel preparation using mucilage and carbopol in different ratios. and i studies indicated high skin retention and penetration rates within the skin for tests niosomal gel formulations (G1 & G2). The present study suggested that developed topical gel formulation provides enhance permeability and longer duration of drug action over conventional gels.

摘要

非离子表面活性剂囊泡的结构框架由基于非离子表面活性剂的微观层状结构组成,这种结构具有维持药物从其递送系统中发挥作用的潜力。在当前的工作中,人们试图确定不同成分的影响,如吐温类和天然黏液对所开发的非离子表面活性剂囊泡凝胶制剂性能的影响,以延长药物的作用持续时间,并将其局部常规给药的副作用降至最低。所有负载布洛芬的非离子表面活性剂囊泡制剂均采用乙醚注入法制备;使用鲸蜡硬脂醇与不同变体的吐温和司盘。进行了各种评估参数以确认非离子表面活性剂囊泡的形成。此外,将非离子表面活性剂囊泡掺入凝胶体系中,并通过膜扩散法对切除的大鼠皮肤进行体外渗透研究(),以及通过角叉菜胶诱导的大鼠足趾肿胀模型进行体内研究。最佳选择的非离子表面活性剂囊泡制剂F9没有出现沉淀、分层和颗粒形状不变的情况,因此选择使用不同比例的黏液和卡波姆制备凝胶。体外和体内研究表明,测试的非离子表面活性剂囊泡凝胶制剂(G1和G2)在皮肤内具有较高的皮肤滞留率和渗透率。本研究表明,所开发的局部凝胶制剂比传统凝胶具有更高的渗透性和更长的药物作用持续时间。

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