RAFT‐Mediated Emulsion Polymerization‐Induced Self‐Assembly for the Synthesis of Core‐Degradable Waterborne Particles

Author:

Galanopoulo Paul1ORCID,Gil Noémie2,Gigmes Didier2ORCID,Lefay Catherine2ORCID,Guillaneuf Yohann2ORCID,Lages Maëlle3,Nicolas Julien3ORCID,D'Agosto Franck1ORCID,Lansalot Muriel1ORCID

Affiliation:

1. Univ Lyon Université Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France

2. Aix Marseille Univ, CNRS Institut de Chimie Radicalaire UMR 7273 Marseille France

3. Université Paris-Saclay, CNRS Institut Galien Paris-Saclay 91400 Orsay France

Abstract

AbstractPoly(N‐acryloylmorpholine) (PNAM)‐decorated waterborne nanoparticles comprising a core of either degradable polystyrene (PS) or poly(n‐butyl acrylate) (PBA) were synthesized by polymerization‐induced self‐assembly (PISA) in water. A PNAM bearing a trithiocarbonate chain end (PNAM‐TTC) was extended via reversible addition‐fragmentation chain transfer (RAFT)‐mediated emulsion copolymerization of either styrene (S) or n‐butyl acrylate (BA) with dibenzo[c,e]oxepane‐5‐thione (DOT). Well‐defined amphiphilic block copolymers were obtained. The in situ self‐assembly of these polymers resulted in the formation of stable nanoparticles. The insertion of thioester units in the vinylic blocks enabled their degradation under basic conditions. The same strategy was then applied to the emulsion copolymerization of BA with DOT using a poly(ethylene glycol) (PEG) equipped with a trithiocarbonate end group, resulting in PEG‐decorated nanoparticles with degradable PBA‐based cores.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

Subject

General Medicine

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