We have developed a new experimental methodology to investigate the adhesive properties of hydrogels on solid surfaces under fully immersed conditions. The method, based on contact mechanics, provides time-resolved reproducible and quantitative data on the work of adhesion between a hydrogel at swelling equilibrium and a planar surface grafted with responsive brushes. We used poly(N,Ndimethylacrylamide) (PDMA) and polyacrylamide (PAM) as model gels and poly(acrylic acid) (PAA) as pH dependent polymer brush. The effect of pH, contact time and debonding velocity on adhesive interactions was specifically investigated. As expected from molecular interactions, we found that adhesion increased as the pH decreased and this was attributed to the formation of hydrogen bonds at the interface. Surprisingly, however, the buildup of adhesion increased slowly with the time of contact up to one hour and depended markedly on debonding velocity despite the very elastic nature of the hydrogels. Furthermore, the maximum pH where adhesion was observed was significantly higher for the couple PAM-PAA than for the couple PDMA-PAA, in contrast with the onset of molecular interactions in dilute solutions.
Polystyrene-block-polychloromethylstyrene (PS-b-PCMS) copolymers, with molecular weights ranging from 4 to 60 kg/mol, were synthesized by nitroxidemediated controlled radical polymerization. Separate aliquots of the PS-b-PCMS samples were quaternized to transform the PCMS block. This resulted in block copolymers with ionizable blocks containing either trimethylammonium chloride or nbutylimidazolium chloride. We refer to ion-containing block copolymers synthesized from the same precursor as matched pairs: SAM (containing trimethylammonium chloride) and SIM (containing n-butylimidazolium chloride). The volume fraction of the ion-containing block, φ, ranges from 0.26 to 0.50 for the case of SAM and from 0.35 to 0.60 for the case of SIM. Self-assembly in these copolymers resulted in the formation of lamellar phases regardless of φ, chemical formula of the bound ion, and chain length. Chloride ion conductivity and water uptake measurements on one of the matched pairs led to similar results. In this matched pair, the changes in conductivity are reported as the chloride ions are replaced by hydroxide ions.
The development of non-cellularized composites of chitosan (CHI) hydrogels, filled with cellulose nanofibers (CNFs) of the type nanofibrillated cellulose, was proposed for the repair and regeneration of the intervertebral disc (IVD) annulus fibrosus (AF) tissue. With the achievement of CNF-filled CHI hydrogels, biomaterial-based implants were designed to restore damaged/degenerated discs. The structural, mechanical and biological properties of the developed hydrogel composites were investigated. The neutralization of weakly acidic aqueous CNF/CHI viscous suspensions in NaOH yielded composites of physical hydrogels in which the cellulose nanofibers reinforced the CHI matrix, as investigated by means of microtensile testing under controlled humidity. We assessed the suitability of the achieved biomaterials for intervertebral disc tissue engineering in ex vivo experiments using spine pig models. Cellulose nanofiber-filled chitosan hydrogels can be used as implants in AF tissue defects to restore IVD biomechanics and constitute contention patches against disc nucleus protrusion while serving as support for IVD regeneration.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.