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用于癌症治疗的载药聚乙二醇-聚乳酸-羟基乙酸共聚物纳米颗粒

Drug-loaded PEG-PLGA nanoparticles for cancer treatment.

作者信息

Zhang Dan, Liu Lin, Wang Jian, Zhang Hong, Zhang Zhuo, Xing Gang, Wang Xuan, Liu Minghua

机构信息

Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.

Pharmaceutical Department of Traditional Chinese Medicine, School of Pharmacy, Southwest Medical University, Luzhou, China.

出版信息

Front Pharmacol. 2022 Aug 19;13:990505. doi: 10.3389/fphar.2022.990505. eCollection 2022.

DOI:10.3389/fphar.2022.990505
PMID:36059964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9437283/
Abstract

Nanoparticles based on single-component synthetic polymers, such as poly (lactic acid-co-glycolic acid) (PLGA), have been extensively studied for antitumor drug delivery and adjuvant therapy due to their ability to encapsulate and release drugs, as well as passively target tumors. Amphiphilic block co-polymers, such as polyethylene glycol (PEG)-PLGA, have also been used to prepare multifunctional nanodrug delivery systems with prolonged circulation time and greater bioavailability that can encapsulate a wider variety of drugs, including small molecules, gene-targeting drugs, traditional Chinese medicine (TCM) and multi-target enzyme inhibitors, enhancing their antitumor effect and safety. In addition, the surface of PEG-PLGA nanoparticles has been modified with various ligands to achieve active targeting and selective accumulation of antitumor drugs in tumor cells. Modification with two ligands has also been applied with good antitumor effects, while the use of imaging agents and pH-responsive or magnetic materials has paved the way for the application of such nanoparticles in clinical diagnosis. In this work, we provide an overview of the synthesis and application of PEG-PLGA nanoparticles in cancer treatment and we discuss the recent advances in ligand modification for active tumor targeting.

摘要

基于单一组分合成聚合物的纳米颗粒,如聚(乳酸-乙醇酸)共聚物(PLGA),因其具有包封和释放药物以及被动靶向肿瘤的能力,已被广泛研究用于抗肿瘤药物递送和辅助治疗。两亲性嵌段共聚物,如聚乙二醇(PEG)-PLGA,也已被用于制备具有延长循环时间和更高生物利用度的多功能纳米药物递送系统,该系统可以包封更广泛的药物,包括小分子、基因靶向药物、中药和多靶点酶抑制剂,从而增强其抗肿瘤效果和安全性。此外,PEG-PLGA纳米颗粒的表面已用各种配体进行修饰,以实现抗肿瘤药物在肿瘤细胞中的主动靶向和选择性积累。用两种配体进行修饰也已应用并具有良好的抗肿瘤效果,而成像剂以及pH响应或磁性材料的使用为这类纳米颗粒在临床诊断中的应用铺平了道路。在这项工作中,我们概述了PEG-PLGA纳米颗粒在癌症治疗中的合成与应用,并讨论了用于主动肿瘤靶向的配体修饰的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/9437283/28d6213a8470/fphar-13-990505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/9437283/e69bade29d24/fphar-13-990505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/9437283/28d6213a8470/fphar-13-990505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/9437283/e69bade29d24/fphar-13-990505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/9437283/28d6213a8470/fphar-13-990505-g002.jpg

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