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Immunocompatibility evaluation of hydrogel-coated polyimide implants for applications in regenerative medicine

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F14%3A00433022" target="_blank" >RIV/61388971:_____/14:00433022 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1002/jbm.a.34873" target="_blank" >http://dx.doi.org/10.1002/jbm.a.34873</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/jbm.a.34873" target="_blank" >10.1002/jbm.a.34873</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Immunocompatibility evaluation of hydrogel-coated polyimide implants for applications in regenerative medicine

  • Original language description

    Immunocompatibility of gelatin-based hydrogels to be applied as implant coatings for local regenerative treatment has been studied. First, the bio- and immuno-acceptability of the methacrylamide-modified gelatin hydrogels per se was screened. The resultsindicated that the hydrogels support cell growth. Metabolic activity of normal cells and permanent cell lines representing various cell types (endothelial, epithelial, fibroblast, and monocyte/macrophage) cultivated on the gelatin hydrogels was moderately lower compared to cells cultivated on tissue culture plastic. The cells cultivated on the hydrogels produced identical cytokines as the control cells although at lower levels. Importantly, no inflammatory activity, measured by nitric oxide and pro-inflammatory cytokine (IL-1, IL-6, and TNF) production, was observed in peritoneal cells and monocyte/macrophage RAW 264.7 cell line cultivated on the hydrogels

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EC - Immunology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP301%2F12%2F1254" target="_blank" >GAP301/12/1254: Overcoming Natural and Multidrug Resistance by Tumor-Selective Delivery of ABC Transporter/Bcl-2 Inhibitors or Therapeutic Gene under PEG-3 Promoter</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Biomedical Materials Research. Part A

  • ISSN

    1549-3296

  • e-ISSN

  • Volume of the periodical

    102

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    1982-1990

  • UT code for WoS article

    000334488800036

  • EID of the result in the Scopus database