用于减轻慢性阻塞性肺疾病的植物源纳米结构药物递送系统:提高关注,最新趋势和比较进展。

IF 3
Madhukar Garg, Pallavi Bassi, Neeraj Mittal, Sandeep Kumar, Piyush Bansal, Neha Sharma, Athrv Arora, Sapna Kumari, Geeta Deswal, Ajmer Singh Grewal
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引用次数: 0

摘要

慢性阻塞性肺疾病(COPD)仍然是一个主要的全球健康负担。虽然常规疗法是有效的,但它们往往与全身副作用、靶特异性差和皮质类固醇抵抗有关。这项研究强调了植物源性生物活性化合物在整合到纳米结构药物传递系统(NDDS)中时改善COPD管理的治疗潜力。这是一篇基于主要电子数据库(PubMed, Scopus, Web of Science和b谷歌Scholar)中截至2025年7月的综合文献检索的叙述性综述。分析的重点是具有抗炎和抗氧化特性的植物化学物质,以及纳米载体,如聚合物纳米颗粒、脂质体和固体脂质纳米颗粒,旨在提高肺部靶向和递送效率。植物化学物质,包括姜黄素、黄芩素、槲皮素、小檗碱和穿心莲内酯,在临床前COPD模型中显示出显著的降低氧化应激和炎症的功效。然而,它们的治疗效用受到溶解性差和快速代谢的阻碍。整合到纳米结构载体中可使肺部积聚增加3-6倍,将药物释放延长至24-48小时,并将给药频率降低约50%,同时最大限度地减少全身毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plant-Derived Nanostructured Drug Delivery Systems for Attenuating Chronic Obstructive Pulmonary Diseases: Raising Concerns, Recent Trends, and Comparative Advancements.

Chronic Obstructive Pulmonary Disease (COPD) remains a major global health burden. Although conventional therapies are effective, they are often associated with systemic side effects, poor target specificity, and corticosteroid resistance. This study emphasizes the therapeutic potential of plant-derived bioactive compounds, when integrated into Nanostructured Drug Delivery Systems (NDDS), for improved COPD management. This is a narrative review based on a comprehensive literature search across major electronic databases (PubMed, Scopus, Web of Science, and Google Scholar) up to July 2025. The analysis focused on phytochemicals with proven anti-inflammatory and antioxidant properties, as well as on nanocarriers such as polymeric nanoparticles, liposomes, and solid lipid nanoparticles, designed to enhance pulmonary targeting and delivery efficiency. Phytochemicals, including curcumin, baicalein, quercetin, berberine, and andrographolide, have shown remarkable efficacy in reducing oxidative stress and inflammation in preclinical COPD models. However, their therapeutic utility is hindered by poor solubility and rapid metabolism. Integration into nanostructured carriers enhanced pulmonary accumulation by 3-6-fold, prolonged drug release up to 24-48 hours, and reduced dosing frequency by approximately 50%, while minimizing systemic toxicity.

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