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

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 co...

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Main Authors: Sarkar, Jit, Chan, Jonathan Kai Bin, Goto, Atsushi
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/147424
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spelling sg-ntu-dr.10356-1474242023-02-28T19:25:03Z Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA Sarkar, Jit Chan, Jonathan Kai Bin Goto, Atsushi School of Physical and Mathematical Sciences Science::Chemistry::Organic chemistry::Polymers Biocompatibility Covalent Bonds 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. National Research Foundation (NRF) Accepted version This work was partly supported by National Research Foundation (NRF) Investigatorship in Singapore (NRF‐NRFI05‐ 2019‐0001). 2021-04-01T01:15:02Z 2021-04-01T01:15:02Z 2021 Journal Article Sarkar, J., Chan, J. K. B. & Goto, A. (2021). Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA. Polymer Chemistry, 12(7), 1060-1067. https://dx.doi.org/10.1039/d0py01764g 1759-9962 https://hdl.handle.net/10356/147424 10.1039/d0py01764g 2-s2.0-85101405472 7 12 1060 1067 en Polymer Chemistry © 2021 Royal Society of Chemistry. All rights reserved. This paper was published in Polymer Chemistry and is made available with permission of Royal Society of Chemistry. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry::Organic chemistry::Polymers
Biocompatibility
Covalent Bonds
spellingShingle Science::Chemistry::Organic chemistry::Polymers
Biocompatibility
Covalent Bonds
Sarkar, Jit
Chan, Jonathan Kai Bin
Goto, Atsushi
Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
description 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.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Sarkar, Jit
Chan, Jonathan Kai Bin
Goto, Atsushi
format Article
author Sarkar, Jit
Chan, Jonathan Kai Bin
Goto, Atsushi
author_sort Sarkar, Jit
title Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
title_short Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
title_full Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
title_fullStr Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
title_full_unstemmed Reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via RCMP-PISA
title_sort reduction-responsive double hydrophilic block copolymer nano-capsule synthesized via rcmp-pisa
publishDate 2021
url https://hdl.handle.net/10356/147424
_version_ 1759855834954727424