Targeted Delivery of Anticancer Therapeutics with Polymers by Harnessing Tumor Microenvironment Acidity

被引:3
|
作者
Shi, Jiahao [1 ]
Ma, Bin [1 ]
Zhang, Yuhe [1 ]
Yong, Haiyang [1 ]
Li, Zhili [1 ]
Sigen, A. [1 ,2 ]
Huang, Xiaobei [3 ]
Zhou, Dezhong [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Shaanxi, Peoples R China
[2] Anhui Univ Sci & Technol, Sch Med, Huainan 232001, Anhui, Peoples R China
[3] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
基金
中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; DRUG-DELIVERY; GENE DELIVERY; CONJUGATED POLYMER; MESOPOROUS SILICA; BLOCK-COPOLYMER; MICELLES; DOXORUBICIN; RELEASE; NANOPARTICLES;
D O I
10.1021/acs.chemmater.3c01151
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cancer therapy is a global biomedical challenge, anda number ofpromising anticancer therapeutics, such as small-molecule drugs, proteins,nucleic acids, photothermal agents, etc., have beendeveloped or are in development. However, the direct administrationof anticancer therapeutics often fails to achieve the desired therapeuticefficacy due to their low bioavailability and poor tissue selectivity,leading to relapse or severe side effects such as immunosuppression,chronic inflammatory responses, mutagenesis, and long-term tissuedysfunction. Polymers offer multiple advantageous properties for thedelivery of anticancer therapeutics but are generally poorly targetedto the tumor microenvironment (TME). The relatively lower acidityof the TME compared to normal tissue provides an intrinsic yet highlyspecific trigger for the development of polymers for the targeteddelivery of anticancer therapeutics. Here, we summarize the exquisitestrategies for the synthesis of TME acidity-sensitive polymers, elucidatethe mechanisms of the polymers' response to TME acidity, andhighlight the applications of the polymers for the delivery of variousanticancer therapeutics. Moreover, the potential challenges in translatingthe polymers into clinical practice are discussed.
引用
收藏
页码:6573 / 6590
页数:18
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