Main-chain degradable, pH-responsive and covalently cross-linked nanoparticles via a one-step RAFT-based radical ring-opening terpolymerization

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Main-chain degradable, pH-responsive and covalently cross-linked nanoparticles via a one-step RAFT-based radical ring-opening terpolymerization
Title:
Main-chain degradable, pH-responsive and covalently cross-linked nanoparticles via a one-step RAFT-based radical ring-opening terpolymerization
Journal Title:
European Polymer Journal
Publication Date:
28 November 2019
Citation:
Jackson, A. W.; Chennamaneni, L. R.; Thoniyot, P., Main-chain degradable, pH-responsive and covalently cross-linked nanoparticles via a one-step RAFT-based radical ring-opening terpolymerization. European Polymer Journal 2020, 122, Article no.: 109391, DOI: 10.1016/j.eurpolymj.2019.109391.
Abstract:
Stimuli-responsive polymeric nanoparticles are very attractive materials often developed for the uptake and controlled release of active molecules, especially in personal and consumer care, agriculture and biomedical applications. However, a significant challenge for polymer scientists is the incorporation of specific functionality and stimuli-responsiveness, while simultaneously including a degradability mechanism to prevent undesirable build-up of the nanoparticle after its specific function is complete. We report, a straightforward synthetic strategy for the preparation of pH-responsive and covalently cross-linked polymeric nanoparticles possessing degradable ester-links in the main-chain of their linear polymer building blocks. This is achieved by combining reversible-addition fragmentation chain-transfer (RAFT) polymerization of conventional vinyl monomers with radical ring-opening polymerization of a cyclic ketene acetal monomer. A PEGylated macro-RAFT chain transfer agent facilitates the radical copolymerization of 2-(diethylamino)ethyl methacrylate, N-hydroxysuccinimide ester methacrylic acid and 2-methylene-1,3-dioxepane affording stimuli-responsive and activated ester functional copolymers which possess ester bonds periodically within their main-chain. These polymers undergo pH-triggered self-assembly. Subsequent, nanoparticle covalent cross-linked is achieved via amide bond formation, while maintaining a degradability mechanism through hydrolysis of the main-chain ester bonds.
License type:
http://creativecommons.org/licenses/by-nc-nd/4.0/
Funding Info:
This work was supported by the Industry Alignment Fund - Pre-Positioning Programme (IAF-PP) of Agency for Science, Technology and Research (A*STAR) (A1786a0025).
Description:
ISSN:
0014-3057
1873-1945
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