- Enzymatically cross-linked hydrogels based on synthetic poly(.alpha.-…
Number of the records: 1  

Enzymatically cross-linked hydrogels based on synthetic poly(.alpha.-amino acid)s functionalized with RGD peptide for 3D mesenchymal stem cell culture

  1. 1.
    SYSNO ASEP0541734
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEnzymatically cross-linked hydrogels based on synthetic poly(.alpha.-amino acid)s functionalized with RGD peptide for 3D mesenchymal stem cell culture
    Author(s) Dvořáková, Jana (UMCH-V) RID, ORCID
    Trousil, Jiří (UMCH-V) RID, ORCID
    Podhorská, Bohumila (UMCH-V) ORCID
    Mikšovská, Zuzana (UMCH-V)
    Janoušková, Olga (UMCH-V) RID, SAI, ORCID
    Proks, Vladimír (UMCH-V) RID, ORCID
    Source TitleBiomacromolecules. - : American Chemical Society - ISSN 1525-7797
    Roč. 22, č. 4 (2021), s. 1417-1431
    Number of pages15 s.
    Languageeng - English
    CountryUS - United States
    Keywordspoly(α-amino acid) ; enzymatic cross-linking ; enzymatic degradation
    Subject RIVEI - Biotechnology ; Bionics
    OECD categoryBioproducts (products that are manufactured using biological material as feedstock) biomaterials, bioplastics, biofuels, bioderived bulk and fine chemicals, bio-derived novel materials
    R&D ProjectsGA18-03224S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000640310700008
    EID SCOPUS85103370049
    DOI https://doi.org/10.1021/acs.biomac.0c01641
    AnnotationInjectable hydrogel scaffolds combined with stem cell therapy represent a promising approach for minimally invasive surgical tissue repair. In this study, we developed and characterized a fully synthetic, biodegradable poly(N5-(2-hydroxyethyl)-l-glutamine)-based injectable hydrogel modified with integrin-binding arginine–glycine–aspartic acid (RGD) peptide (PHEG-Tyr-RGD). The biodegradable hydroxyphenyl polymer precursor derivative of PHEG-Tyr was enzymatically cross-linked to obtain injectable hydrogels with different physicochemical properties. The gelation time, gel yield, swelling behavior, and storage modulus of the PHEG-Tyr hydrogels were tuned by varying the concentrations of the PHEG-Tyr precursors and horseradish peroxidase as well as the nH2O2/nTyr ratio. The mechanical properties and gelation time of the PHEG-Tyr hydrogel were optimized for the encapsulation of rat mesenchymal stem cells (rMSCs). We focused on the 2D and 3D spreading and viability of rMSCs within the PHEG-Tyr-RGD hydrogels with different physicochemical microenvironments in vitro. Encapsulation of rMSCs shows long-term survival and exhibits cell–matrix and cell–cell interactions reflective of both the RGD concentration and hydrogel stiffness. The presented biomaterial represents a suitable biological microenvironment to guide 3D spreading and may act as a promising 3D artificial extracellular matrix for stem cell therapy.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2022
    Electronic addresshttps://pubs.acs.org/doi/10.1021/acs.biomac.0c01641
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.