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关于通过不同给药途径增强硝酸戊四唑纳米系统抗真菌活性的最新综述。

A comprehensive review on recent nanosystems for enhancing antifungal activity of fenticonazole nitrate from different routes of administration.

机构信息

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

出版信息

Drug Deliv. 2023 Dec;30(1):2179129. doi: 10.1080/10717544.2023.2179129.

Abstract

This review aims to comprehensively highlight the recent nanosystems enclosing Fenticonazole nitrate (FTN) and to compare between them regarding preparation techniques, studied factors and responses. Moreover, the optimum formulae were compared in terms of and studies in order to detect the best formula. FTN is a potent antifungal imidazole compound that had been used for treatment of many dangerous fungal infections affecting eye, skin or vagina. FTN had been incorporated in various innovative nanosystems in the recent years in order to achieve significant recovery such as olaminosomes, novasomes, cerosomes, terpesomes and trans-novasomes. These nanosystems were formulated by various techniques (ethanol injection or thin film hydration) utilizing different statistical designs (Box-Behnken, central composite, full factorial and D-optimal). Different factors were studied in each nanosystem regarding its composition as surfactant concentrations, surfactant type, amount of oleic acid, cholesterol, oleylamine, ceramide, sodium deoxycholate, terpene concentration and ethanol concentration. Numerous responses were studied such as percent entrapment efficiency (EE%), particle size (PS), poly-dispersity index (PDI), zeta potential (ZP), and drug release. Selection of the optimum formula was based on numerical optimization accomplished by Design-Expert® software taking in consideration the largest EE %, ZP (as absolute value) and drug release and lowest PS and PDI. comparisons were done employing different techniques such as Transmission electron microscopy, pH determination, effect of gamma sterilization, elasticity evaluation and docking study. In addition to, permeation, irritancy test, histopathological, antifungal activity and Kinetic study.

摘要

本文旨在全面总结最近将硝酸芬替康唑(FTN)封装在纳米系统中的研究,并就制备技术、研究因素和反应对它们进行比较。此外,还比较了最佳配方在和研究方面的差异,以检测最佳配方。FTN 是一种有效的抗真菌咪唑化合物,已被用于治疗许多影响眼睛、皮肤或阴道的危险真菌感染。近年来,FTN 已被纳入各种创新的纳米系统中,以实现显著的恢复,如 olaminosomes、novasomes、cerosomes、terpesomes 和 trans-novasomes。这些纳米系统是通过各种技术(乙醇注入或薄膜水化),利用不同的统计设计(Box-Behnken、中心复合、完全因子和 D-最优)来制备的。在每个纳米系统中,都针对其组成(表面活性剂浓度、表面活性剂类型、油酸、胆固醇、油胺、神经酰胺、脱氧胆酸钠、萜烯浓度和乙醇浓度)研究了不同的因素。研究了许多响应,如包封效率(EE%)、粒径(PS)、多分散指数(PDI)、Zeta 电位(ZP)和药物释放。最佳配方的选择是基于通过 Design-Expert®软件完成的数值优化,考虑到最大的 EE%、ZP(绝对值)和药物释放以及最低的 PS 和 PDI。还进行了比较,采用了不同的技术,如透射电子显微镜、pH 值测定、伽马灭菌效果、弹性评估和对接研究。此外,还进行了渗透、刺激性试验、组织病理学、抗真菌活性和动力学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bffb/9930819/f9ec6a1c6da3/IDRD_A_2179129_F0001_C.jpg

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