首页> 外文期刊>Acta pharmaceutica: a quarterly journal of Croatian Pharmaceutical Society and Slovenian Pharmaceutical Society, dealing with all branches of pharmacy and allied sciences >Alkyl polyglucoside vs. ethoxylated surfactant-based microemulsions as vehicles for two poorly water-soluble drugs: physicochemical characterization and in vivo skin performance
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Alkyl polyglucoside vs. ethoxylated surfactant-based microemulsions as vehicles for two poorly water-soluble drugs: physicochemical characterization and in vivo skin performance

机译:烷基聚葡糖苷与乙氧基化表面活性剂的微乳液作为两种水溶性药物的载体:物理化学表征和体内皮肤性能

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摘要

Two types of biocompatible surfactants were evaluated for their capability to formulate skin-friendly/non-irritant microemulsions as vehicles for two poorly water-soluble model drugs differing in properties and concentrations: alkyl polyglucosides (decyl glucoside and caprylyl/capryl glucoside) and ethoxylated surfactants (glycereth-7-caprylate/caprate and polysorbate 80). Phase behavior, structural inversion and microemulsion solubilization potential for sertaconazole nitrate and adapalene were found to be highly dependent on the surfactants structure and HLB value. Performed characterization (polarized light microscopy, pH, electrical conductivity, rheological, FTIR and DSC measurements) indicated a formulation containing glycereth-7-caprylate/caprate as suitable for incorporation of both drugs, whereas alkyl polyglucoside-based systems did not exhibit satisfying solubilization capacity for sertaconazole nitrate. Further, monitored parameters were strongly affected by sertaconazole nitrate incorporation, while they remained almost unchanged in adapalene-loaded vehicles. In addition, results of the in vivo skin performance study supported acceptable tolerability for all investigated formulations, suggesting selected microemulsions as promising carriers worth exploring further for effective skin delivery of model drugs.
机译:评价两种类型的生物相容性表面活性剂,以使其能力配制皮肤友好/非刺激性微乳液作为在性能和浓度下不同的水溶性模型药物的载体:烷基多葡糖苷(癸酰葡糖苷和泡甲酰基葡糖苷)和乙氧基化表面活性剂(甘油 - 7-辛酸盐/癸酸盐和聚山梨醇酯80)。发现氨基唑唑和白沙烯的相行为,结构倒置和微乳液溶解电位高度依赖于表面活性剂结构和HLB值。进行表征(偏振光显微镜,pH,电导率,流变学,FTIR和DSC测量)表明含有甘油-7-辛酸酯/癸酸盐的配方,如适合于两种药物的掺入,而基于烷基的基于氧化锆的系统没有表现出满足溶解能力对于硝酸塞康唑唑。此外,受硝酸锡康唑掺入的受监测的参数强烈影响,而它们在加载的载体车辆中仍然保持不变。此外,体内皮肤性能研究的结果支持所有调查的制剂的可接受的耐受性,表明所选微乳液作为可承受的载体,可进一步探索模型药物的有效皮肤递送。

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