角质层
脂质体
化学
神经酰胺
Zeta电位
生物利用度
渗透
色谱法
渗透(战争)
膜
溶解度
硬脂酸
人体皮肤
生物物理学
药理学
生物化学
纳米颗粒
有机化学
材料科学
纳米技术
医学
工程类
病理
生物
细胞凋亡
遗传学
运筹学
作者
Aneta Vovesná,Alexander Zhigunov,Martin Balouch,Jarmila Zbytovská
标识
DOI:10.1016/j.ijpharm.2021.120264
摘要
Diseases related to a disrupted skin barrier are accompanied by lower levels of ceramides in the stratum corneum (SC) lipid matrix. Delivering ceramides directly into damaged skin is a viable alternative to conventional corticosteroids, but is hindered by their low skin bioavailability and limited nanoformulation ability. Here, we developed stable liposomal systems containing ceramides and other SC lipids, and tested their effectiveness in skin barrier repair. Lipid film hydration and high-pressure homogenization were used to prepare different types of liposomes. To determine the stability, the particle size and polydispersity index were measured. The optimal systems were found to include ceramide 3 and 6, cholesterol and stearic acid, with 10% urea in phosphate-buffered saline as the aqueous phase. The ability of the system to repair chemically-damaged porcine skin was tested. While treatment by a standard lipid suspension reduced the passage of a model permeant only to a limited extent, drug flux through the liposomally-treated skin was much closer to permeation through intact skin. The non-homogenized liposomes were more effective than their homogenized version. These findings were also confirmed by FTIR measurements. This suggests that our approach to liposomal development has considerable potential for the repair of a disrupted skin barrier.
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