scholarly journals Micellar nanoparticles with tuneable morphologies through interactions between nucleobase-containing synthetic polymers in aqueous solution

2016 ◽  
Vol 7 (25) ◽  
pp. 4254-4262 ◽  
Author(s):  
Zan Hua ◽  
Anaïs Pitto-Barry ◽  
Yan Kang ◽  
Nigel Kirby ◽  
Thomas R. Wilks ◽  
...  

Herein, we report the preparation of nucleobase-containing synthetic amphiphilic diblock copolymers using RAFT polymerization.

1999 ◽  
Vol 32 (3) ◽  
pp. 697-703 ◽  
Author(s):  
Minoru Nakano ◽  
Hideki Matsuoka ◽  
Hitoshi Yamaoka ◽  
Andreas Poppe ◽  
Dieter Richter

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 827
Author(s):  
Xiaowei An ◽  
Weihong Lu ◽  
Jian Zhu ◽  
Xiangqiang Pan ◽  
Xiulin Zhu

Selenide-containing amphiphilic copolymers have shown significant potential for application in drug release systems. Herein, we present a methodology for the design of a reactive oxygen species-responsive amphiphilic diblock selenide-labeled copolymer. This copolymer with controlled molecular weight and narrow molecular weight distribution was prepared by sequential organoselenium-mediated reversible addition fragmentation chain transfer (Se-RAFT) polymerization and selenol-based nucleophilic reaction. Nuclear magnetic resonance (NMR) and matrix-assisted laser desorption/ionization time-to-flight (MALDI-TOF) techniques were used to characterize its structure. Its corresponding nanomicelles successfully formed through self-assembly from the copolymer itself. Such nanomicelles could rapidly disassemble under oxidative conditions due to the fragmentation of the Se–C bond. Therefore, this type of nanomicelle based on selenide-labeled amphiphilic copolymers potentially provides a new platform for drug delivery.


2018 ◽  
Vol 266 ◽  
pp. 628-639 ◽  
Author(s):  
Raphael Henrique Marques Marcilli ◽  
Ana Paula Rodrigues Camilo ◽  
Cesar Liberato Petzhold ◽  
Maria Isabel Felisberti

2010 ◽  
Vol 63 (8) ◽  
pp. 1159 ◽  
Author(s):  
Jun Ma ◽  
Jeremy W. Bartels ◽  
Zhou Li ◽  
Ke Zhang ◽  
Chong Cheng ◽  
...  

With an ever increasing interest in the combined functionality and versatility of materials, increasing demands are placed on synthetic methodologies by which to produce such materials. This work demonstrates the preparation of block copolymers having fluorocarbon content, pyrrolidinone units, and alkene groups as complex building blocks for the assembly of discrete nanoparticles in solution and, alternatively, transformation into sophisticated crosslinked networks. Reversible addition–fragmentation chain transfer (RAFT) polymerization is a facile tool for the synthesis of well-defined polymers containing imbedded side-chain functionalities. In this work, the synthesis of well-defined multifunctional fluorinated polymers bearing pendant pyrrolidinone groups, and block copolymers bearing both pyrrolidinone and alkenyl groups on different segments was achieved, by using RAFT polymerizations of unique bifunctional monomers. Upon micellization, the amphiphilic diblock copolymers were transformed into regioselectively-functionalized nanoparticles. Further transformations of pyrrolidinone- and alkene-dual functionalized-block copolymers into complex amphiphilic networks were accomplished by highly efficient UV-induced thiol-ene reactions. Whether as discrete nanoparticles or nanoscopically-segregated crosslinked networks, these materials have great potential for several diverse technologies, including as anti-fouling materials.


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