Microwave Irradiation-Assisted Reversible Addition-Fragmentation Chain Transfer Polymerization-Induced Self-Assembly of PH-Responsive Diblock Copolymer Nanoparticles

Overview

Journal ACS Omega

Publisher American Chemical Society

Specialty Chemistry

Date 2022 Dec 5

PMID 36467927

Authors

Svetlana Lukas Petrova

Vladimir Sincari

Rafal Konefal

Ewa Pavlova

Martin Hruby

Vaclav Pokorny

Eliezer Jager

Affiliations

Soon will be listed here.

Abstract

Herein, we present a versatile platform for the synthesis of pH-responsive poly([-(2-hydroxypropyl)]methacrylamide)--poly[2-(diisopropylamino)ethyl methacrylate] diblock copolymer (PHPMA--PDPA) nanoparticles (NPs) obtained via microwave-assisted reversible addition-fragmentation chain transfer polymerization-induced self-assembly (MWI-PISA). The -(2-hydroxypropyl) methacrylamide (HPMA) monomer was first polymerized to obtain a macrochain transfer agent with polymerization degrees (DPs) of 23 and 51. Subsequently, using mCTA and 2-(diisopropylamino)ethyl methacrylate (DPA) as monomers, we successfully conducted MWI-PISA emulsion polymerization in aqueous solution with a solid content of 10 wt %. The NPs were obtained with high monomer conversion and polymerization rates. The resulting diblock copolymer NPs were analyzed by dynamic light scattering (DLS) and cryogenic-transmission electron microscopy (cryo-TEM). cryo-TEM studies reveal the presence of only NPs with spherical morphology such as micelles and polymer vesicles known as polymersomes. Under the selected conditions, we were able to fine-tune the morphology from micelles to polymersomes, which may attract considerable attention in the drug-delivery field. The capability for drug encapsulation using the obtained in situ pH-responsive NPs, the polymersomes based on PHPMA--PDPA, and the micelles based on PHPMA--PDPA was demonstrated using the hydrophobic agent and fluorescent dye as Nile red (NR). In addition, the NP disassembly in slightly acidic environments enables fast NR release.

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