The mechanical performances of hydrogels are greatly influenced by the functionality of cross-linkers and their covalent and non-covalent interactions with the polymer chains. Conventional chemical cross-linkers fail to meet the demand of large toughness and high extensibility for their immediate applications as artificial tissues like ligaments, blood vessels, and cardiac muscles in human or animal bodies. Herein, we synthesized a new graphene oxide-based two-dimensional (2D) cross-linker (GOBC) and exploited the functionality of the cross-linker for the enhancement of toughness and stretchability of a poly(acrylic acid) (PAA) hydrogel. The 2D nanosheets of GO were modified in such a way that they could provide multifunctional sites for both physical and chemical bonding with the polymer chains. Carboxylic acid groups at the surfaces of the GO sheets were coupled with the acrylate functional groups for covalent cross-linking, while the other oxygen-containing functional groups are responsible for physical cross-linking with polymers. The GOBC had been successfully incorporated into the PAA hydrogel and the mechanical properties of the GOBC cross-linked PAA hydrogel (PAA-GOBC) were investigated at various compositions of cross-linker. Seven times enhancement in both toughness and elongation at break has been achieved without compromising on the modulus for the as-synthesized PAA-GOBC compared to the conventional ,'-methylenebis(acrylamide) (MBA) cross-linked PAA hydrogel. This facile and efficient way of GO modification is expected to lead the development of a high-performance nanocomposite for cutting-edge applications in biomedical engineering.
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http://dx.doi.org/10.1039/d0ra00678e | DOI Listing |
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December 2024
School of Nuclear Science and Technology, University of Science and Technology of China, Hefei, 230026, China.
Hydrogels present significant potential in flexible materials designed for electromagnetic interference (EMI) shielding, attributed to their soft, stretchable mechanical properties and water-rich porous structures. Unfortunately, EMI shielding hydrogels commonly suffer from low mechanical properties, deficient fracture energy, and low strength, which limit the serviceability of these materials in complex mechanical environments. In this study, the double network strategy is successfully utilized along with the Hofmeister effect to create MXene/PAA (polyacrylic acid)-CS (chitosan) hydrogels and further strengthen and toughen the gel with (NH)SO solution.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830017, Xinjiang, PR China. Electronic address:
Stretchable conductive hydrogels have attracted great attention in flexible electronics. Nevertheless, conductive hydrogels would suffer from an inevitable damage during use, significantly reducing the reliability and limiting the practicability. Herein, stretchable and self-healing conductive hydrogels are designed form carboxymethyl cellulose (CMC), polyacrylic acid (PAA), and Fe, which are applied for monitoring human motions and electrophysiological signals.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Guilin University of Technology, Coll Chem & Bioengn, Guangxi, Guilin 541004, China; Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, China.
Conductive hydrogels based on sodium alginate (SA) have potential applications in human activity monitoring and personal medical diagnosis due to their good conductivity and flexibility. However, most sensing SA-hydrogels exhibit poor mechanical properties and lack of self-healing, self-adhesive, and antibacterial properties, greatly limiting their practical applications. Therefore, in this paper, a multifunctional double-network PAA-SA hydrogel consisting of poly(acrylic acid) (PAA) and sodium alginate (SA) was prepared by a simple strategy.
View Article and Find Full Text PDFColloids Surf B Biointerfaces
December 2024
College of Chemistry and Materials Science, Fujian Normal University, Fuzhou 350007, PR China; Fujian Provincial Key Laboratory of Polymer Materials, Fujian Normal University, Fuzhou 350007, PR China. Electronic address:
Hemostasis and subsequent anti-inflammatory measures are essential for wound healing in the human body following trauma or surgical procedures. Here, we try to use the dragging effect of a brush to prepare a Janus hydrogel with the least amount of bacteriostatic agent. The synthesized suspension of polyvinylbenzene-silica@quaternary ammonium salt (PDVB-SiO@NR) Janus particles (JNPs) was selected as ink and brush coated onto one side of a polyacrylic acid (PAA) hydrogel, resulting in Janus hydrogel (JNPs≌PAA).
View Article and Find Full Text PDFColloids Surf B Biointerfaces
December 2024
Laboratory of Bio & Nano Materials, Drug Delivery and Controlled Release, Department of Microbiology, Faculty of Health Sciences, University of Talca, Talca, Chile. Electronic address:
Hydrogels (HGs) are 3-D polymeric networks with high water content, making them appropriate for biomedical applications such as drug delivery systems. This study examines the impact of agarose in semi-interpenetrating polymer networks (Semi-IPNs) based on poly(acrylic acid) (p(AA)), N, N' Methylenebis(acrylamide) (MBA) and agarose (AGA) on the sustained release of Polymyxin B (PolB). Agarose incorporation improved the mechanical strength, swelling behavior and drug retention capacity of the HG.
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