Development of Niosomal Vesicles Loaded Mometasone Furoate Gel for Transdermal Delivery and its Evaluation.

Bhushan R Rane, Pushkar Y Chavan, Nidhi S Kate, Ashish S Jain
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Abstract

Background: Mometasone Furoate (MF) is a corticosteroid (glucocorticoid) used to treat eczema, psoriasis, allergies, and rash on the skin; also used to reduce itching, redness, and swelling (inflammation). It has been reported that the bioavailability of MF is less than 11% when given via the nasal route. Encapsulating the drug in niosomes can improve the active pharmaceutical ingredient's bioavailability by enhancing both physical and biological stability.

Objective: The goal of the study is to develop, a non-ionic surfactant-based vesicular system, by loading mometasone furoate, and introducing it into a gel-based formulation by utilizing an appropriate gelling agent, and performing its evaluation.

Methods: The niosome vesicle was prepared by vacuum rotary evaporation method (Thin film hydration method). Gel was prepared using the dispersion method and in-vitro drug diffusion studies using Franz-diffusion cells.

Results: According to the results of the experiments conducted for the study, Mometasone Furoate niosomal gel was prepared utilizing Mometasone Furoate niosomes that were made using the thin film hydration process, Cholesterol, and Span 60, and loaded in various amounts of Carbopol as a geling agent. The niosomes' zeta potential was found to be -24 mV, showing that the formulation is stable. The polydispersity index (PDI) was found to be 0.409 and the average size of niosomes to be 252.7 nm. The performance of the gel of the optimized formulations containing 2% Carbopol showed in vitro diffusion for 7 hours and an increased flux rate as compared to the plain MF.

Conclusion: The experiments carried out during the study led to the conclusion that the thin-film hydration method was suitable for the formation of the MF-niosomes by using Span 60 and Cholesterol (2:1). The gel formulation containing 2% Carbopol indicated better in vitro diffusion following the Higuchi model across all niosomal gel formulations. Niosomal gel can be regarded as the best vesicular carrier for the efficient distribution of mometasone furoate via the transdermal route.

膜小体载糠酸莫米松凝胶经皮给药的研制及其评价。
背景:糠酸莫米松(MF)是一种皮质类固醇(糖皮质激素),用于治疗湿疹、牛皮癣、过敏和皮肤皮疹;也用于减轻瘙痒、红肿(炎症)。据报道,经鼻给药时,MF的生物利用度低于11%。将药物包埋在纳米体中可以通过提高药物的物理和生物稳定性来提高活性药物成分的生物利用度。目的:本研究的目的是通过负载糠酸莫米松,并通过适当的胶凝剂将其引入凝胶基配方,并对其进行评估,从而开发一种非离子表面活性剂为基础的囊泡系统。方法:采用真空旋转蒸发法(薄膜水化法)制备膜小体囊泡。凝胶采用分散法制备,体外弗兰兹扩散细胞进行药物扩散研究。结果:根据本研究的实验结果,采用薄膜水合工艺、胆固醇、Span 60制备糠酸莫米松乳质体,并以不同量的卡波醇为胶凝剂,制备糠酸莫米松乳质体凝胶。纳米体的zeta电位为-24 mV,表明该制剂是稳定的。多分散性指数(PDI)为0.409,粒体的平均尺寸为252.7 nm。结果表明,含2%卡波波尔的优化配方凝胶的体外扩散时间为7小时,通量比普通MF增加。结论:本研究中所进行的实验表明,以Span 60和胆固醇(2:1)为原料,薄膜水化法适用于MF-niosomes的形成。根据Higuchi模型,含有2%卡波波尔的凝胶制剂在所有乳质体凝胶制剂中具有更好的体外扩散。乳质体凝胶是糠酸莫米松经皮有效分布的最佳囊泡载体。
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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CiteScore
2.40
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