Pristine gelatin incorporation as a strategy to enhance the biofunctionality of poly(vinyl alcohol)-based hydrogels for tissue engineering applications

• Published in: Biomaterials science Vol. 12; no. 1; pp. 134 - 15
• Main Authors: Longoni, Alessia, Major, Gretel S, Jiang, Shaoyuan, Farrugia, Brooke L, Kieser, David C, Woodfield, Tim B. F, Rnjak-Kovacina, Jelena, Lim, Khoon S
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 19.12.2023
• Subjects: Animals; Biocompatible Materials - chemistry; Biocompatible Materials - pharmacology; Biomedical materials; Blood vessels; Chemical properties; Constraining; Controlled release; Endothelial cells; Ethanol; Gelatin; Gelatin - chemistry; Growth factors; Hydrogels; Hydrogels - chemistry; Infiltration; Mice; Physical properties; Polymers - chemistry; Polyvinyl alcohol; Polyvinyl Alcohol - chemistry; Surgical implants; Tissue Engineering; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A
• ISSN: 2047-4830; 2047-4849
• DOI: 10.1039/d3bm01172k

Synthetic polymers, such as poly(vinyl alcohol) (PVA), are popular biomaterials for the fabrication of hydrogels for tissue engineering and regenerative medicine (TERM) applications, as they provide excellent control over the physico-chemical properties of the hydrogel. However, their bioinert nature is known to limit cell-biomaterial interactions by hindering cell infiltration, blood vessel recruitment and potentially limiting their integration with the host tissue. Efforts in the field have therefore focused on increasing the biofunctionality of synthetic hydrogels, without limiting the advantages associated with their tailorability and controlled release capacity. The aim of this study was to investigate the suitability of pristine gelatin to enhance the biofunctionality of tyraminated PVA (PVA-Tyr) hydrogels, by promoting cell infiltration and host blood vessel recruitment for TERM applications. Pure PVA-Tyr hydrogels and PVA-Tyr hydrogels incorporated with vascular endothelial growth factor (VEGF), a well-known pro-angiogenic stimulus, were used for comparison. Incorporating increasing concentrations of VEGF (0.01-10 μg mL −1 ) or gelatin (0.01-5 wt%) did not influence the physical properties of PVA-Tyr hydrogels. However, their presence within the polymer network (>0.1 μg mL −1 VEGF and >0.1 wt% gelatin) promoted endothelial cell interactions with the hydrogels. The covalent binding of unmodified gelatin or VEGF to the PVA-Tyr network did not hamper their inherent bioactivity, as they both promoted angiogenesis in a chick chorioallantoic membrane (CAM) assay, performing comparably with the unbound VEGF control. When the PVA-Tyr hydrogels were implanted subcutaneously in mice, it was observed that cell infiltration into the hydrogels was possible in the absence of gelatin or VEGF at 1- or 3-weeks post-implantation, highlighting a clear difference between in vitro an in vivo cell-biomaterial interaction. Nevertheless, the presence of gelatin or VEGF was necessary to enhance blood vessel recruitment and infiltration, although no significant difference was observed between these two biological molecules. Overall, this study highlights the potential of gelatin as a standalone pro-angiogenic cue to enhance biofunctionality of synthetic hydrogels and provides promise for their use in a variety of TERM applications. In this study, we investigated the suitability of pristine gelatin to enhance the biofunctionality of tyraminated PVA hydrogels, by promoting cell infiltration and host blood vessel recruitment in vitro and in vivo for tissue engineering applications.