离体
渗透
体内
渗透(战争)
肺表面活性物质
材料科学
溶解度
色谱法
泊洛沙姆407
Zeta电位
生物医学工程
泊洛沙姆
胶束
分散性
化学
药理学
水溶液
纳米技术
膜
医学
生物化学
共聚物
纳米颗粒
有机化学
高分子化学
数学
生物技术
运筹学
复合材料
生物
聚合物
作者
Nihal Farid Younes,Sally A. Abdel-Halim,Abdelhalim I. Elassasy
出处
期刊:Drug Delivery
[Taylor & Francis]
日期:2018-01-01
卷期号:25 (1): 1706-1717
被引量:73
标识
DOI:10.1080/10717544.2018.1497107
摘要
Keratomycosis is a serious corneal disease that can cause a permanent visual disability if not treated effectively. Sertaconazole nitrate (STZ), a novel broad spectrum antifungal drug, was suggested as a promising treatment. However, its utility in the ocular route is restricted by its poor solubility, along with other problems facing the ocular delivery like short residence time, and the existing corneal barrier. Therefore, the objective of this study was to formulate STZ loaded binary mixed micelles (STZ-MMs) enriched with different penetration enhancers using thin-film hydration method, based on a 31.22 mixed factorial design. Different formulation variables were examined, namely, type of auxiliary surfactant, type of penetration enhancer, and total surfactants: drug ratio, and their effects on the solubility of STZ in MMs (SM), particle size (PS), polydispersity index (PDI), and zeta potential (ZP) were evaluated. STZ-MMs enhanced STZ aqueous solubility up to 338.82-fold compared to free STZ. Two optimized formulations (MM-8 and MM-11) based on the desirability factor (0.891 and 0.866) were selected by Design expert® software for further investigations. The optimized formulations were imaged by TEM which revealed nanosized spherical micelles. Moreover, they were examined for corneal mucoadhesion, stability upon dilution, storage effect, and ex vivo corneal permeation studies. Finally, both in vivo corneal uptake and in vivo corneal tolerance were investigated. MM-8 showed superiority in the ex vivo and in vivo permeation studies when compared to the STZ-suspension. The obtained results suggest that the aforementioned STZ loaded mixed micellar system could be an effective candidate for Keratomycosis-targeted therapy.
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