Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized: Via RCMP-PISA

Jit Sarkar, Kai Bin Jonathan Chan, Atsushi Goto*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

A double hydrophilic block copolymer (DHBC) vesicle was synthesized via an organocatalyzed living radical polymerization, i.e., reversible complexation mediated polymerization (RCMP). RCMP was combined with polymerization-induced self-assembly (PISA) to give an amphiphilic block copolymer vesicle comprising hydrophilic poly(poly(ethylene glycol) methyl ether methacrylate) (PPEGMA) and hydrophobic poly(solketal methacrylate) (PSKM). With the incorporation of a crosslinker, i.e., bis(2-methacryloyl)oxyethyl disulfide (BMOD), in the vesicle, and upon the subsequent hydrolysis of the hydrophobic PSKM into hydrophilic poly(glycerol methacrylate) (PGLMA), a stable DHBC vesicle was generated. The vesicle was successfully utilized to encapsulate an external guest molecule. The encapsulated molecule was also released by cleaving the disulfide bond in the crosslinker (BMOD) in the presence of glutathione (in a reductive condition). The present vesicle consists of neutral (not acidic or basic) PEGMA and PGLMA segments and hence has no restriction in the pH range for its use. PPEGMA and PGLMA are also biocompatible. With these properties, the present DHBC vesicle may serve as a useful reduction-responsive container.

Original languageEnglish
Pages (from-to)1060-1067
Number of pages8
JournalPolymer Chemistry
Volume12
Issue number7
DOIs
Publication statusPublished - Feb 21 2021
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

ASJC Scopus Subject Areas

  • Bioengineering
  • Biochemistry
  • Polymers and Plastics
  • Organic Chemistry

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