Department of Pharmaceutics & Pharmaceutical Technology, Shree S. K. Patel College of Pharmaceutical Education & Research, Ganpat University, Kherva, Gujarat, 384012, India.
Department of Pharmaceutics, Sanjivani College of Pharmaceutical Education & Research, Kopargaon, Maharashtra , 423603, India.
Ther Deliv. 2024;15(9):667-683. doi: 10.1080/20415990.2024.2379756. Epub 2024 Aug 5.
This study focuses on the development of a Caspofungin liposome for efficient ocular delivery by enhancing corneal penetration. Quality by design (QbD) approach was adopted to identify critical factors that influence final liposomal formulation. The liposome developed using thin film hydration after optimization was subjected to characterization for physicochemical properties, irritation potential and corneal uptake. The numerical optimization suggests an optimal formulation with a desirability value of 0.706, using CQAs as optimization goals with 95% prediction intervals. The optimized formulation showed no signs of irritation potential along with observation of significant corneal permeation. The liposomal formulation increased the permeability of Caspofungin, which could enhance the efficacy for the treatment of conditions, like fungal keratitis.
本研究专注于通过增强角膜穿透性来开发一种卡泊芬净脂质体,以实现高效的眼部递药。采用质量源于设计(QbD)方法来确定影响最终脂质体配方的关键因素。经过优化的薄膜水化法制备的脂质体进行理化性质、刺激性和角膜摄取的表征。数值优化表明,使用 CQAs 作为优化目标,具有 95%预测区间的理想配方具有 0.706 的理想值。优化后的配方没有表现出刺激性,同时观察到角膜穿透性有显著提高。脂质体配方增加了卡泊芬净的通透性,这可以提高治疗真菌性角膜炎等疾病的疗效。