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含低浓度亲脂性聚合物乳化剂的多重W/O/W乳液体系的特性及药物释放性能研究

An investigation into the characteristics and drug release properties of multiple W/O/W emulsion systems containing low concentration of lipophilic polymeric emulsifier.

作者信息

Vasiljevic Dragana, Parojcic Jelena, Primorac Marija, Vuleta Gordana

机构信息

Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, Belgrade University, Vojvode Stepe 450, 11221 Belgrade-Kumodraz, Serbia and Montenegro.

出版信息

Int J Pharm. 2006 Feb 17;309(1-2):171-7. doi: 10.1016/j.ijpharm.2005.11.034. Epub 2006 Jan 6.

Abstract

Multiple W/O/W emulsions with high content of inner phase (Phi1=Phi2=0.8) were prepared using relatively low concentrations of lipophilic polymeric primary emulsifier, PEG 30-dipolyhydroxystearate, and diclofenac diethylamine (DDA) as a model drug. The investigated formulations were characterized and their stability over the time was evaluated by dynamic and oscillatory rheological measurements, microscopic analysis and in vitro drug release study. In vitro release profiles of the selected model drug were evaluated in terms of the effective diffusion coefficients and flux of the released drug. The multiple emulsion samples exhibited good stability during the ageing time. Concentration of the lipophilic primary emulsifier markedly affected rheological behaviour as well as the droplet size and in vitro drug release kinetics of the investigated systems. The multiple emulsion systems with highest concentration (2.4%, w/w) of the primary emulsifier had the lowest droplet size and the highest apparent viscosity and highest elastic characteristics. Drug release data indicated predominately diffusional drug release mechanism with sustained and prolonged drug release accomplished with 2.4% (w/w) of lipophilic emulsifier employed.

摘要

使用相对低浓度的亲脂性聚合物初级乳化剂聚乙二醇30 - 二聚羟基硬脂酸酯以及双氯芬酸二乙胺(DDA)作为模型药物,制备了内相含量高(Phi1 = Phi2 = 0.8)的多重水包油包水型乳液。对所研究的制剂进行了表征,并通过动态和振荡流变学测量、显微镜分析以及体外药物释放研究评估了它们随时间的稳定性。根据释放药物的有效扩散系数和通量评估了所选模型药物的体外释放曲线。多重乳液样品在老化期间表现出良好的稳定性。亲脂性初级乳化剂的浓度显著影响所研究体系的流变行为以及液滴大小和体外药物释放动力学。初级乳化剂浓度最高(2.4%,w/w)的多重乳液体系具有最小的液滴尺寸、最高的表观粘度和最高的弹性特性。药物释放数据表明主要是扩散性药物释放机制,使用2.4%(w/w)的亲脂性乳化剂可实现药物的持续和延长释放。

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