Issue 14, 2018

Novel triple responsive polybenzimidazole synthesized via amine-ene Michael addition

Abstract

Responsive polymers have significant importance and promising applications in the field of biomedicine. In this study, benzimidazole (BI)-based polyesters were synthesized for the first time via amine-ene click polycondensation. Benzimidazolethione (BITO) and aliphatic diacrylates (DA) were selected as clickable monomers using the organic catalyst 4-dimethylaminopyridine (DMAP) to obtain benzimidazole-based polyesters. 1,4-Butylene diacrylate (BDA) and poly(ethylene glycol) diacrylate (PEGDA) were used as model DA to synthesize lipophilic and hydrophilic polymers, respectively. Furthermore, click polymerization of BITO with BDA and PEGDA was conducted for tricomponent polycondensation. 1H NMR, FTIR and GPC spectra demonstrated that the BITO-based polyesters were successfully synthesized via the click condensation of amine-ene. The obtained polymers exhibited pH, reactive oxygen species (ROS) and β-cyclodextrin (β-CD) triple responsiveness and the amphiphilic BITO polyester can self-assemble into nanoparticles. We believe that these novel BITO polyesters have great potential as drug delivery systems for controlled drug release in nanomedicine.

Graphical abstract: Novel triple responsive polybenzimidazole synthesized via amine-ene Michael addition

Article information

Article type
Paper
Submitted
31 Mar 2018
Accepted
24 May 2018
First published
25 May 2018

New J. Chem., 2018,42, 11396-11403

Novel triple responsive polybenzimidazole synthesized via amine-ene Michael addition

L. Gao, W. Wang, B. Yu and H. Cong, New J. Chem., 2018, 42, 11396 DOI: 10.1039/C8NJ01571F

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