Innovative hyaluronic acid-decorated quatsomes for enhanced renal targeting: design, optimization and in-vivo biochemical and nephroprotective assessments.

IF 5.5 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Journal of Pharmacy and Pharmaceutical Sciences Pub Date : 2026-07-24 eCollection Date: 2026-01-01 DOI:10.3389/jpps.2026.16787
Sadek Ahmed, Rana M ElBishbishy, Mohamed A Sadek, Osama Saher
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引用次数: 0

Abstract

The kidney plays a critical role in metabolite excretion, fluid regulation, and homeostasis, yet remains highly vulnerable to structural and functional disorders. Kidney diseases represent a major global health burden, often progressing to chronic complications due to the limited efficacy and poor selectivity of conventional therapies, which are frequently associated with systemic toxicity. Accordingly, the development of targeted drug delivery systems is essential to improve therapeutic outcomes. In this study, advanced quatsomes were developed as a kidney-targeted nanosystem to enhance the delivery of curcumin, a natural polyphenolic compound with potent antioxidant and nephroprotective properties. The system was composed of di-dodecyl-dimethyl-ammonium bromide (DDAB), cholesterol, limonene, hyaluronic acid (HA) and surfactants, and was fabricated using the ethanol injection method. A 23 factorial design was employed to optimize formulation variables, including DDAB:cholesterol ratio, limonene:drug ratio, and surfactant concentration. The optimized formulation (desirability = 0.950) exhibited high entrapment efficiency (87.80%), nanosized vesicles (120.55 nm), and a positive surface charge (+38.30 mV). Transmission electron microscopy confirmed spherical morphology, while in-vitro release studies demonstrated a biphasic profile. The formulation also showed good physicochemical stability and enhanced antioxidant activity. Mechanistically, passive targeting via nanoscale size and cationic charge facilitated interaction with the glomerular filtration barrier and mesangial uptake, while limonene improved vesicle deformability. HA functionalization further enabled CD44-mediated active targeting. In vivo, the optimized system significantly reduced serum creatinine and blood urea nitrogen levels in a cisplatin-induced nephrotoxicity model, with histological evidence of renal protection. Overall, the developed quatsomes demonstrate promising potential as an efficient renal-targeted nanocarrier.

创新透明质酸修饰的准体增强肾脏靶向:设计,优化和体内生化和肾保护评估。
肾脏在代谢产物排泄、体液调节和体内平衡中起着至关重要的作用,但仍然极易受到结构和功能障碍的影响。肾脏疾病是一项主要的全球健康负担,由于常规治疗的疗效有限和选择性差,往往发展为慢性并发症,这往往与全身毒性有关。因此,开发靶向给药系统对于改善治疗效果至关重要。在这项研究中,先进的准体被开发为肾脏靶向纳米系统,以增强姜黄素的传递,姜黄素是一种具有有效抗氧化和肾保护特性的天然多酚化合物。该体系由二十二烷基二甲基溴化铵(DDAB)、胆固醇、柠檬烯、透明质酸(HA)和表面活性剂组成,采用乙醇注射法制备。采用23因子设计优化处方变量,包括DDAB:胆固醇比、柠檬烯:药物比和表面活性剂浓度。优化后的配方(理想度= 0.950)具有较高的包封效率(87.80%)、纳米尺寸(120.55 nm)和表面正电荷(+38.30 mV)。透射电子显微镜证实球形形态,而体外释放研究显示双相轮廓。该配方具有良好的理化稳定性和抗氧化活性。在机制上,通过纳米级尺寸和阳离子电荷的被动靶向促进了与肾小球滤过屏障和系膜摄取的相互作用,而柠檬烯改善了囊泡的变形能力。HA功能化进一步激活了cd44介导的主动靶向。在体内,优化后的系统在顺铂诱导的肾毒性模型中显著降低了血清肌酐和血尿素氮水平,具有肾保护的组织学证据。总的来说,开发的准体作为一种有效的肾脏靶向纳米载体显示出很大的潜力。
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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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
29
审稿时长
6-12 weeks
期刊介绍: The Journal of Pharmacy and Pharmaceutical Sciences (JPPS) is the official journal of the Canadian Society for Pharmaceutical Sciences. JPPS is a broad-spectrum, peer-reviewed, international pharmaceutical journal circulated electronically via the World Wide Web. Subscription to JPPS is free of charge. Articles will appear individually as soon as they are accepted and are ready for circulation.
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