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Efficacy Tumor Therapeutic Applications of Stimuli-responsive Block Copolymer-based Nano-assemblies

Overview
Journal Heliyon
Specialty Social Sciences
Date 2024 Apr 4
PMID 38571609
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Abstract

Block copolymers are composed of two or more blocks or segments with different chemical properties via various chemical bonds, which can assemble into nanoparticles with a "core-shell" structure. Due to the benefits of simple functionalization, superior drug-loading capacity, and good biocompatibility, various nano-assemblies based on block copolymers have become widely applied in the treatment of cancers in recent years. These nano-assemblies serve as carriers for anti-tumor bioactive, enhancing drug stability and prolonging their circulation time in vivo, which can reduce the toxic side effects of drugs and improve the therapeutic effect. However, the complex and heterogeneous tumor microenvironment poses challenges to the therapeutic efficacy of these nano-assemblies, having the result in the occurrence of drug resistance and the recurrence of tumors. Consequently, a diverse array of stimuli-responsive nano-assemblies has been devised in order to surmount these obstacles. This article provides a comprehensive overview of the utilization of stimuli-responsive nano-assemblies derived from block copolymers in the context of tumor treatment. The review summarizes block polymers responsive to internal stimuli (like ROS, redox, pH, and enzymes) and external stimuli (like light, and temperature), and discusses current challenges and prospects in this field, aiming to provide novel insights for clinical applications.

References
1.
Zhao J, Peng Y, Diaz-Dussan D, White J, Duan W, Kong L . Zwitterionic Block Copolymer Prodrug Micelles for pH Responsive Drug Delivery and Hypoxia-Specific Chemotherapy. Mol Pharm. 2021; 19(6):1766-1777. DOI: 10.1021/acs.molpharmaceut.1c00518. View

2.
Yang X, Du J, Dou S, Mao C, Long H, Wang J . Sheddable ternary nanoparticles for tumor acidity-targeted siRNA delivery. ACS Nano. 2011; 6(1):771-81. DOI: 10.1021/nn204240b. View

3.
Ge Z, Liu S . Functional block copolymer assemblies responsive to tumor and intracellular microenvironments for site-specific drug delivery and enhanced imaging performance. Chem Soc Rev. 2013; 42(17):7289-325. DOI: 10.1039/c3cs60048c. View

4.
Tan J, Deng Z, Song C, Xu J, Zhang Y, Yu Y . Coordinating External and Built-In Triggers for Tunable Degradation of Polymeric Nanoparticles via Cycle Amplification. J Am Chem Soc. 2021; 143(34):13738-13748. DOI: 10.1021/jacs.1c05617. View

5.
Zhou Q, Xiang J, Qiu N, Wang Y, Piao Y, Shao S . Tumor Abnormality-Oriented Nanomedicine Design. Chem Rev. 2023; 123(18):10920-10989. DOI: 10.1021/acs.chemrev.3c00062. View