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聚乙二醇化聚乳酸-羟基乙酸共聚物纳米颗粒:开启癌症治疗的先进策略

PEGylated PLGA nanoparticles: unlocking advanced strategies for cancer therapy.

作者信息

Kesharwani Prashant, Kumar Vishal, Goh Khang Wen, Gupta Garima, Alsayari Abdulrhman, Wahab Shadma, Sahebkar Amirhossein

机构信息

Department of Pharmaceutical Sciences, Dr. Harisingh Gour Vishwavidyalaya, Sagar, Madhya Pradesh, 470003, India.

Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, 110062, India.

出版信息

Mol Cancer. 2025 Jul 24;24(1):205. doi: 10.1186/s12943-025-02410-x.

Abstract

Poly(lactic-co-glycolic acid) (PLGA) is a widely utilized biodegradable and biocompatible polymer in drug delivery systems, particularly for encapsulating drug molecules with poor solubility and permeability. PLGA nanoparticles, composed of polylactic acid (PLA) and polyglycolic acid (PGA), offer tunable properties such as controlled degradation rates and drug release kinetics. The PEGylation of PLGA nanoparticles results in the formation of a polyethylene glycol (PEG) corona on their surface, which enhances systemic circulation by reducing opsonization and immune system recognition. This extended circulation time increases the likelihood of nanoparticles reaching the target site, a crucial advantage in cancer therapy, as it allows for reduced dosage frequency while improving therapeutic efficacy. Furthermore, surface functionalization with targeting ligands enables selective delivery to specific cells or organs via ligand-receptor interactions, facilitating enhanced cellular uptake and intracellular drug release. This review provides a comprehensive analysis of PEGylated PLGA nanoparticles in cancer diagnosis and therapy, highlighting recent advancements, current challenges, and future perspectives in their clinical translation.

摘要

聚乳酸-乙醇酸共聚物(PLGA)是药物递送系统中广泛使用的可生物降解且具有生物相容性的聚合物,尤其用于封装溶解性和渗透性较差的药物分子。由聚乳酸(PLA)和聚乙醇酸(PGA)组成的PLGA纳米颗粒具有可调节的特性,如可控的降解速率和药物释放动力学。PLGA纳米颗粒的聚乙二醇化导致其表面形成聚乙二醇(PEG)冠,通过减少调理作用和免疫系统识别来增强全身循环。这种延长的循环时间增加了纳米颗粒到达靶位点的可能性,这在癌症治疗中是一个关键优势,因为它允许减少给药频率,同时提高治疗效果。此外,用靶向配体进行表面功能化能够通过配体-受体相互作用将药物选择性递送至特定细胞或器官,促进增强的细胞摄取和细胞内药物释放。本文综述对聚乙二醇化PLGA纳米颗粒在癌症诊断和治疗中的应用进行了全面分析,重点介绍了其近期进展、当前挑战以及临床转化的未来前景。

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