含莫匹罗星乳液凝胶的设计、研制与表征

Hardik A. Lakkad, V. Patel
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引用次数: 1

摘要

本研究的目的是开发更有效的莫匹罗星给药系统。为取得有效的配方,正在进行研究。莫匹罗星是一种抗微生物剂,用于伤口愈合治疗。首先对SEDDS的油、表面活性剂和助表面活性剂进行了筛选。用紫外分光光度法考察了药物在不同油脂、表面活性剂和助表面活性剂中的溶解度。将药物溶解在溶解度最大的油中,然后加入溶解度最大的表面活性剂和助表面活性剂,在磁力搅拌器上搅拌均匀。形成透明的SEDDS。卡波波尔940和聚丙烯酸钠胶凝剂分别悬浮在水中,水合过夜。在制备乳凝胶时,设定了不同的凝胶与sedds的比例。测定凝胶的药物释放率、pH值和药物含量。结果表明,乳凝胶具有较好的控释效果。处方F11释药率为99.27%,ph值为6.7±0.1,药物含量为99.4±0.11%。优选配方F11为最佳配方。乳凝胶的配方对局部应用具有很好的治疗效果。
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Design Development and Characterisation of Mupirocin Loaded Emulsion Based Gel
The objective of the present study was to develop more retentive and effective drug delivery system for mupirocin. The research was going on in achieving effective formulation. Mupirocin is an anti-microbial agent that is used in wounds healing treatment. First Screening of oil, surfactant and co-surfactant for SEDDS carried out. Solubility of drug was investigated in different oils, surfactant and co-surfactants by UV method. A drug was dissolved in available oil in which it exhibited maximum solubility, then surfactant and co-surfactant were added in which drug showed maximum solubility, mixed well on a magnetic stirrer. Transparent SEDDS were formed. Carbopol 940 and Polyacrylate sodium gelling agent was suspended in water and hydrated for overnight separately. For preparation of Emulgel, various ratios of gel and SEDDS were set. Emulgel was evaluated for %drug release, pH, and drug content. The results indicated that Emulgel gave better controlled release. The formulation F11 showed 99.27 percent drug release, pH 6.7 ± 0.1 and drug content 99.4 ± 0.11%. Formulation F11 was selected as an optimized formulation. The formulations of Emulgel delivered very good therapeutic efficacy for topical application.
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