Protein Adsorption, Calcium-Binding Ability, and Biocompatibility of Silver Nanoparticle-Loaded Polyvinyl Alcohol (PVA) Hydrogels Using Bone Marrow-Derived Mesenchymal Stem Cells

dc.contributor.authorElango, Jeevithan
dc.contributor.authorZamora, Camilo
dc.contributor.authorAlexis, Frank
dc.contributor.authorWu, Wenhui
dc.contributor.authorMaté Sánchez de Val, José Eduardo
dc.date.accessioned2026-04-14T12:34:41Z
dc.date.available2026-04-14T12:34:41Z
dc.date.issued2023-06-28
dc.description.abstractSeveral approaches have evolved to facilitate the exploration of hydrogel systems in biomedical research. In this sense, poly(vinyl alcohol) (PVA) has been widely used in hydrogel (HG) fabrication for several therapeutic applications. The biological properties of PVA hydrogels (PVA-HGs) are highly dependent on their interaction with protein receptors and extracellular matrix (mainly calcium) deposition, for which there is not enough evidence from existing research yet. Thus, for the first time, the functional properties, like protein and mineral interactions, related to the proliferation of mesenchymal stem cells (MSCs) by silver nanoparticle (AgNP)-loaded PVA hydrogels (AgNPs-PVA-HGs) were investigated in the present study. The UV absorption spectrum and TEM microscopic results showed a maximum absorbance of synthesized AgNPs at 409 nm, with an average particle size of 14.5 ± 2.5 nm, respectively. The functional properties, such as the calcium-binding and the protein adsorption of PVA-HG, were accelerated by incorporating AgNPs; however, the swelling properties of the HGs were reduced by AgNPs, which might be due to the masking of the free functional groups (hydroxyl groups of PVA) by AgNPs. SEM images showed the presence of AgNPs with a more porous structure in the HGs. The proliferative effect of MSCs increased over culture time from day 1 to day 7, and the cell proliferative effect was upregulated by HGs with more pronounced AgNPs-PVA-HG. In addition, both HGs did not produce any significant cytotoxicity in the MSCs. The histological (bright light and H&E staining) and fluorescence microscopic images showed the presence of a cytoskeleton and the fibrillar structure of the MSCs, and the cells adhered more firmly to all HGs. More fibrillar bipolar and dense fibrillar structures were seen in the day 1 and day 7 cultures, respectively. Interestingly, the MSCs cultured on AgNPs-PVA-HG produced extracellular matrix deposition on day 7. Accordingly, the present results proved the biocompatibility of AgNPs-PVA-HG as a suitable system for culturing mammalian stem cells for regenerative tissue applications.es
dc.description.disciplineOdontologíaes
dc.description.facultyCiencias de la Saludes
dc.identifier.citationElango, J., Zamora-Ledezma, C., Alexis, F., Wu, W., & Maté-Sánchez De Val, J. E. (2023). Protein adsorption, calcium-binding ability, and biocompatibility of silver nanoparticle-loaded polyvinyl alcohol (Pva) hydrogels using bone marrow-derived mesenchymal stem cells. Pharmaceutics, 15(7), 1843. https://doi.org/10.3390/pharmaceutics15071843es
dc.identifier.doi10.3390/pharmaceutics15071843es
dc.identifier.urihttp://hdl.handle.net/10952/10973
dc.issue.number7es
dc.journal.titlePharmaceuticses
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectPVAes
dc.subjectAgNPses
dc.subjectHydrogeles
dc.subjectMesemchymal stem cellses
dc.subjectProtein and mineral interactones
dc.titleProtein Adsorption, Calcium-Binding Ability, and Biocompatibility of Silver Nanoparticle-Loaded Polyvinyl Alcohol (PVA) Hydrogels Using Bone Marrow-Derived Mesenchymal Stem Cellses
dc.typejournal articlees
dc.type.hasVersionAMes
dc.volume.number15es
dspace.entity.typePublication
person.affiliation.nameUniversidad Católica San Antonio de Murcia
person.affiliation.nameUniversidad Católica San Antonio de Murcia
person.identifier.orcid0000-0003-4115-9918
person.identifier.orcid0000-0002-4216-421X
relation.isAuthorOfPublicationd603b380-cf33-4b35-aeb4-253be882d276
relation.isAuthorOfPublication1a5339db-97e4-4a13-bcce-99953be8fd67
relation.isAuthorOfPublication.latestForDiscoveryd603b380-cf33-4b35-aeb4-253be882d276

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