Menthol-based Novel Ultra-Deformable Vesicle: Formulation, Optimization and Evaluation of an Antifungal Drug

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Hema Manjushree, Devika Nayak, Praveen Halagali, Mahalaxmi Rathnanand, Roshan Tawale, Koteshwara Ananthmurthy, Jesil Mathew Aranjani, Vamshi Krishna Tippavajhala
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Abstract

The current study aims to establish a novel ultra-deformable vesicular system to enhance the drug penetration across the skin by preparing the ketoconazole-loaded menthosomes. It was achieved through regular thin-film evaporation & hydration techniques. To examine the effect of formulation parameters on menthosome characteristics, a 23 full factorial design was used using Design-Expert® software. The optimized batch exhibited a vesicle size (107.6 nm), a polydispersity index (PDI) (0.248), entrapment efficiency (% EE) (76.9%), and a zeta potential (-33.7 mV). Results from ex vivo skin permeation studies and in vitro drug release demonstrated enhanced improved skin permeation and drug release compared to other formulations. An in vitro antifungal and in vivo pharmacodynamic study, elucidated the enhanced effectiveness of the optimized formulation against Candida albicans. In summary, menthosomes could serve as a potent vehicle to enhance drug penetration via the skin to improve its antifungal activity.

Graphical Abstract

基于薄荷醇的新型超变形囊泡:一种抗真菌药物的配方、优化和评价
本研究旨在通过制备酮康唑薄荷糖体,建立一种新型的超变形囊泡系统,以提高药物在皮肤中的渗透能力。这是通过常规薄膜蒸发实现的。水化技术。为了检验配方参数对薄荷素特性的影响,使用design - expert®软件进行了23全因子设计。优化后的微泡大小为107.6 nm,多分散指数(PDI)为0.248,包封效率(% EE)为76.9%,zeta电位为-33.7 mV。体外皮肤渗透研究和体外药物释放的结果表明,与其他配方相比,该配方可以增强皮肤渗透和药物释放。体外抗真菌和体内药效学研究表明,优化后的制剂对白色念珠菌具有较强的抗真菌作用。综上所述,薄荷糖可以作为一种有效的载体来增强药物通过皮肤的渗透,从而提高其抗真菌活性。图形抽象
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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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