Self-assembling amphiphilic PEGylated block copolymers obtained through RAFT polymerization for drug-delivery applications

被引:0
|
作者
Colombo C. [1 ]
Gatti S. [2 ]
Ferrari R. [3 ]
Casalini T. [1 ]
Cuccato D. [1 ]
Morosi L. [3 ]
Zucchetti M. [3 ]
Moscatelli D. [2 ]
机构
[1] Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 1, Zürich
[2] Dipartimento di Chimica, Materiali Ed Ingegneria Chimica, Politecnico di Milano, Milano
[3] IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, Milano
来源
Moscatelli, Davide (davide.moscatelli@polimi.it) | 1600年 / John Wiley and Sons Inc卷 / 133期
关键词
copolymers; drug-delivery systems; self-assembly;
D O I
10.1002/app.43084
中图分类号
学科分类号
摘要
In this work, ring-opening polymerization and reversible addition-fragmentation chain transfer polymerization (RAFT) have been employed for the production of block copolymers where the backbone is brushed with poly(ethylene glycol) (PEG) and polyester chains. Because of their amphiphilic properties, they are able to self-assemble in water, forming micelles. Molecular dynamics simulations have been accomplished to study the behavior of the copolymer single chain in water, and the self-assembly properties have been characterized and correlated to the copolymer structure in terms of critical micellar concentration and particle size. As a proof of their flexibility, these materials have been employed for the production of polymer-lipid hybrid nanoparticles with tunable dimensions (from 120 to 260 nm) adopted for the controlled release of anticancer compounds (paclitaxel and curcumin). © 2015 Wiley Periodicals, Inc.
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