Tailoring Hydrogel Sheet Properties through Co-Monomer Selection in AMPS Copolymer Macromers

Abstract

This study investigates hydrogels based on 2-Acrylamido-2-methyl-1-propanesulfonic acid sodium salt (AMPS) copolymers, incorporating N-hydroxyethyl acrylamide (HEA) and 3-sulfopropyl acrylate potassium salt (SPA). The addition of HEA and SPA is designed to fine-tune the hydrogels’ water absorption and mechanical properties, ultimately enhancing their characteristics and expanding their potential for biomedical applications. A copolymer of AMPS, 2-carboxyethyl acrylate (CEA) combined with methacrylic acid (MAA) as poly(AMPS-stat-CEA-stat-MAA, PACM), was preliminarily synthesized. CEA and MAA were modified with allyl glycidyl ether (AGE) through ring-opening, yielding macromers with pendant allyl groups (PACM-AGE). Copolymers poly(AMPS-stat-HEA-stat-CEA-stat-MAA) (PAHCM) and poly(AMPS-stat-SPA-stat-CEA-stat-MAA) (PASCM) were also synthesized and modified with AGE to produce PAHCM-AGE and PASCM-AGE macromers. These copolymers and macromers were characterized by 1H NMR, FT-IR, and GPC, confirming successful synthesis and functionalization. The macromers were then photocrosslinked into hydrogels and evaluated for swelling, water content, and mechanical properties. The results revealed that the PASCM-AGE hydrogels exhibited superior swelling ratios and water retention, achieving equilibrium water content (~92%) within 30 min. While the mechanical properties of HEA and SPA containing hydrogels show significant differences compared to PACM-AGE hydrogel (tensile strength 2.5 MPa, elongation 47%), HEA containing PAHCM-AGE has a higher tensile strength (5.8 MPa) but lower elongation (19%). In contrast, SPA in the PASCM-AGE hydrogels led to both higher tensile strength (3.7 MPa) and greater elongation (92%), allowing for a broader range of hydrogel properties. An initial study on drug delivery behavior was conducted using PACM-AGE hydrogels loaded with photosensitizers, showing effective absorption, release, and antibacterial activity under light exposure. These AMPS-based macromers with HEA and SPA modifications demonstrate enhanced properties, making them promising for wound management and drug delivery applications.

Publication DOI: https://doi.org/10.3390/polym16172522
Divisions: College of Engineering & Physical Sciences > School of Infrastructure and Sustainable Engineering > Chemical Engineering & Applied Chemistry
College of Engineering & Physical Sciences > Aston Polymer Research Group
College of Engineering & Physical Sciences > Aston Advanced Materials
College of Engineering & Physical Sciences > Aston Institute of Materials Research (AIMR)
College of Engineering & Physical Sciences
Aston University (General)
Funding Information: This work was supported by Thailand Science Research and Innovation (TSRI) (Grant Number FRB660001/0179, Contract Number R2566B004), Global and Frontier Research University (Grant Number R2566C052), and Naresuan University, and this project has also recei
Additional Information: Copyright © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Uncontrolled Keywords: hydrogels,macromers,2-acrylamido-2-methylpropane sulfonic acid sodium salt,photosensitizer,biomedical applications
Publication ISSN: 2073-4360
Data Access Statement: The data presented in this study are available on request from the corresponding author. The data are not publicly available due to the data forms part of an ongoing study.
Last Modified: 19 Dec 2024 08:23
Date Deposited: 01 Oct 2024 17:19
Full Text Link:
Related URLs: https://www.mdp ... 4360/16/17/2522 (Publisher URL)
PURE Output Type: Article
Published Date: 2024-09
Published Online Date: 2024-09-05
Accepted Date: 2024-09-03
Authors: Daengmankhong, Jinjutha
Pinthong, Thanyaporn
Promkrainit, Sudarat
Yooyod, Maytinee
Mahasaranon, Sararat
Punyodom, Winita
Ross, Sukunya
Jongjitwimol, Jirapas
Tighe, Brian J. (ORCID Profile 0000-0001-9601-8501)
Derry, Matthew J. (ORCID Profile 0000-0001-5010-6725)
Topham, Paul D. (ORCID Profile 0000-0003-4152-6976)
Ross, Gareth M.

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