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Cytocompatible Hydrogels with Tunable Mechanical Strength and Adjustable Swelling Properties through Photo-Cross-Linking of Poly(vinylphosphonates). | LitMetric

Cytocompatible Hydrogels with Tunable Mechanical Strength and Adjustable Swelling Properties through Photo-Cross-Linking of Poly(vinylphosphonates).

ACS Appl Mater Interfaces

Technical University of Munich, Germany, TUM School of Natural Sciences, Department of Chemistry, WACKER-Chair of Macromolecular Chemistry, Lichtenbergstraße 4, 85748 Garching, Germany.

Published: October 2024

AI Article Synopsis

  • A new synthetic hydrogel was developed by cross-linking poly(vinylphosphonates) using controlled polymerization methods and photoinitiated thiol-ene click chemistry, allowing for precise adjustments in composition and properties.
  • The resulting hydrogels showed increased mechanical strength with more specific monomer units, but reduced water absorption due to increased hydrophobicity; however, functionalization improved water uptake significantly.
  • The final hydrogels demonstrated compatibility for cell growth, enabling adhesion of human umbilical artery smooth muscle cells and forming an endothelial layer without inducing inflammatory responses or losing antibacterial properties.

Article Abstract

Herein, the synthesis, characterization, and application of a novel synthetic hydrogel based on the photoinitiated cross-linking of poly(vinylphosphonates) is presented. First, statistical copolymers with adjustable ratios of the monomers diallyl vinylphosphonate (DAlVP) and diethyl vinylphosphonate (DEVP), as well as different molecular weights, were obtained via rare earth metal-mediated group-transfer polymerization (REM-GTP) while maintaining narrow polydispersities. The copolymers were cross-linked by applying photoinitiated thiol-ene click chemistry (λ = 365 nm). The network formation was monitored via oscillatory rheology coupled with UV-irradiation, revealing the high spatiotemporal control of the reaction. Moreover, the equilibrium storage moduli of poly(vinylphosphonate)-based hydrogels increased with a growing number of DAlVP units and upon application of a different cross-linker, which was additionally confirmed by nanoindentation experiments. In contrast, the water uptake of hydrogels decreased with higher DAlVP amounts in the corresponding hydrogels due to lower chain mobility and an overall increase in the hydrophobicity of the samples. Upon successful functionalization of P(DEVP--DAlVP) copolymers with sodium 3-mercaptopropane-1-sulfonate, as indicated via H DOSY NMR, the respective cross-linked materials displayed a remarkable increase in the water uptake; thus, presenting highly hydrophilic gels with an apparent interplay between water uptake, cross-linking density, and functionalization degree. Finally, the purified hydrogels showed cytocompatibility and enabled cell adhesion of human umbilical artery smooth muscle cells (HUASMCs) after direct seeding. The materials further allowed the adhesion and growth of an endothelial layer, triggered no pro-inflammatory response as evidenced by cytokine release of M0 macrophages, and exhibited antibacterial properties toward and .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11533175PMC
http://dx.doi.org/10.1021/acsami.4c07860DOI Listing

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