Effect of surfactants on the characteristics of fluconazole niosomes for enhanced cutaneous delivery.

Madhu Gupta, Bhuvaneshwar Vaidya, Neeraj Mishra, Suresh P Vyas
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引用次数: 66

Abstract

Fluconazole-loaded niosomes were prepared by the film hydration method with different surfactants (Span and Brij series) and characterized for various parameters. Results showed that niosomes composed of Span 40, Span 60, and Brij 72 were most stable with smaller size, i.e. 0.378 ± 0.022 μm, 0.343 ± 0.063 μm, and 0.287 ± 0.012 μm, respectively, along with higher entrapment efficiency (approx. > 41%). In vitro skin permeation and retention studies suggested that cutaneous accumulation was affected by surfactant property and vesicle size. Therefore the niosomes consisting of Span 40, Span 60, and Brij 72 surfactant are seemingly accumulated and form localized drug depots in the skin, thereby releasing the contents in a sustained manner and able to greatly enhance cutaneous retention of the drug.

表面活性剂对氟康唑niosomes增强皮肤给药特性的影响。
采用不同表面活性剂(Span和Brij系列)的膜水合法制备了负载氟康唑的niosomes,并对其进行了不同参数的表征。结果表明,由Span 40、Span 60和Brij 72组成的膜小体最稳定,膜小体尺寸较小,分别为0.378±0.022 μm、0.343±0.063 μm和0.287±0.012 μm。> 41%)。体外皮肤渗透和滞留研究表明,皮肤蓄积受表面活性剂性质和囊泡大小的影响。因此,由Span 40、Span 60和Brij 72表面活性剂组成的膜小体在皮肤中似乎积累并形成局部药物库,从而持续释放内容物,并能够大大增强药物在皮肤中的潴留。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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