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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Development of microemulsion based topical ivermectin formulations: Preformulation and formulation studies
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Development of microemulsion based topical ivermectin formulations: Preformulation and formulation studies

机译:基于微乳液的局部Ivermectin配方的研制:预先形成和配制研究

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The aim of this work was to develop microemulsions and microemulsion gels which can be used as vehicles for the topical delivery of ivermectin. Tea tree oil and ethyl butanoate were found to be suitable for ivermectin-loaded microemulsion formulations due to the higher solubility of ivermectin in these two oils than other tested oils. The pseudo-ternary phase diagrams were constructed based on these selected oils and combination of different surfactant/co-surfactant at different ratios. Ivermectin-loaded stable microemulsions and microemulsion gels were successfully formulated based on the selected compositions from the phase diagrams. Ivermectin-loaded microemulsions showed spherical nano-droplets dispersed in the continuous phase (via cryogenic field emission scanning electron microscope image) and the particle size was less than 100 nm (via dynamic light scattering measurement). Ethyl butanoate based microemulsion appeared to be the best microemulsion formulation considering the stability and permeation profiles while tea tree oil based microemulsion showed the best stability profile. Overall, microemulsion gel formulations exhibited better stability profiles than their microemulsion counterparts. All microemulsion gel formulations demonstrated significantly faster in vitro membrane permeation (release) rate of ivermectin than Soolantra cream (reference marketed product by Galderma, USA).The developed microemulsion and microemulsion gel formulations appear to be promising vehicles for topical delivery of ivermectin.
机译:这项工作的目的是开发微乳液和微乳液凝胶,可用作伊维菌素局部递送的车辆。发现茶树油和乙醇酸乙酯是适用于伊维菌素负载的微乳液配方,这是伊维菌素在这两种油中较高的伊维菌素比其他测试油的溶解度。基于这些选定的油和不同比例以不同比例的不同表面活性剂/共表面活性剂的组合构建伪半相形图。基于来自相图的所选组合物成功地配制了伊维菌素负载稳定的微乳液和微乳液凝胶。伊维菌素负载的微乳液显示出分散在连续相中的球形纳米液滴(通过低温场发射扫描电子显微镜图像),并且粒径小于100nm(通过动态光散射测量)。基于丁醇酸酯的微乳液似乎是考虑到稳定性和渗透型材的最佳微乳液制剂,而茶树油基微乳液显示最佳稳定性曲线。总的来说,微乳液凝胶制剂比其微乳液对应物显示出更好的稳定性曲线。所有微乳液凝胶制剂的体外膜渗透速度明显更快(释放)伊葡聚糖蛋白的速率(由Galderma,USA的参考销售产品)。显影的微乳液和微乳液凝胶配方似乎是用于局部递送伊维菌素的有前途的车辆。

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