HSPiP and QbD oriented optimized stearylamine-elastic liposomes for topical delivery of ketoconazole to treat deep seated fungal infections: In vitro and ex vivo evaluations

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics: X Pub Date : 2024-08-26 DOI:10.1016/j.ijpx.2024.100279
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Abstract

The study explored stearylamine containing cationic elastic liposomes to improve topical delivery and efficacy of ketoconazole (KETO) to treat deeply seated fungal infections. Stearylamine was used for dual functionalities (electrostatic interaction and flexibility in lipid bilayer). Hansen solubility program (HSPiP) estimated Hansen solubility parameters (HSP) based on the SMILE file and structural properties followed by experimental solubility study to validate the predicted values. Various formulations were developed by varying phosphatidylcholine and surfactants (tween 80 and span 80) concentration. To impart cationic properties, stearylamine (1.0 %) was added into the organic phase. Using quality by design (QbD) method, we optimized the formulations and evaluated for vesicle size, polydispersity index, zeta potential, morphology (scanning electron microscopy), in vitro drug release (%), and ex vivo permeation profiles. Result showed that there is a good correlation (0.65) between HSPiP predicted and actual experimental solubility of KETO in water, chloroform, S80, and tween 80. Spherical OKEL1 showed an established correlation between the predicted and the actual formulation parameters (size, zeta potential, and polydispersity index) (259 nm vs 270 nm, +2.4 vs 0.21 mV, and 0.24 vs 0.27). OKEL1 was associated with the highest value of %EE (83.1 %) as compared to liposomes. Finally, OKEL1 exhibited the highest % cumulative permeation (49.9 %) as compared to DS (13 %) and liposomes (25 %). Moreover, OKEL1 resulted in 4-fold increase in permeation flux as compared to DS which may be attributed to vesicular mediated improved permeation and gel based compensated trans epidermal water loss in the skin. The drug deposition elicited OKEL1 and OKEL1-gel as suitable carriers for maximum therapeutic benefit to treat deeply seated fungal infections.

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以 HSPiP 和 QbD 为导向优化硬脂胺弹性脂质体,用于局部给药酮康唑以治疗深部真菌感染:体外和体内评估
该研究探索了含有硬脂基胺的阳离子弹性脂质体,以改善酮康唑(KETO)的局部给药和疗效,从而治疗深部真菌感染。硬脂胺具有双重功能(静电作用和脂质双分子层中的柔韧性)。汉森溶解度程序(HSPiP)根据 SMILE 文件和结构特性估算出汉森溶解度参数(HSP),然后进行实验溶解度研究以验证预测值。通过改变磷脂酰胆碱和表面活性剂(吐温 80 和 span 80)的浓度,开发出了各种配方。为了赋予其阳离子特性,在有机相中添加了硬脂胺(1.0%)。我们采用质量源于设计(QbD)的方法对配方进行了优化,并对囊泡大小、多分散指数、ZETA电位、形态(扫描电子显微镜)、体外药物释放率(%)和体内外渗透曲线进行了评估。结果表明,HSPiP 预测的 KETO 在水、氯仿、S80 和吐温 80 中的溶解度与实际实验溶解度之间存在良好的相关性(0.65)。球形 OKEL1 的预测值与实际配方参数(尺寸、ZETA 电位和多分散指数)之间存在确定的相关性(259 nm vs 270 nm、+2.4 vs 0.21 mV 和 0.24 vs 0.27)。与脂质体相比,OKEL1 的 %EE 值最高(83.1%)。最后,与 DS(13%)和脂质体(25%)相比,OKEL1 的累积渗透率最高(49.9%)。此外,与 DS 相比,OKEL1 的渗透通量增加了 4 倍,这可能是由于囊泡介导的渗透性提高以及凝胶弥补了皮肤的跨表皮失水所致。药物沉积使 OKEL1 和 OKEL1 凝胶成为治疗深部真菌感染的合适载体,从而获得最大的治疗效果。
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
期刊最新文献
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