Human decellularized and crosslinked pericardium coated with bioactive molecular assemblies
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31665713
DOI
10.1088/1748-605x/ab52db
Knihovny.cz E-zdroje
- MeSH
- alografty MeSH
- biokompatibilní materiály * chemie MeSH
- biomechanika MeSH
- endoteliální buňky pupečníkové žíly (lidské) cytologie metabolismus MeSH
- fibrin MeSH
- fibronektiny MeSH
- glutaraldehyd MeSH
- heterografty MeSH
- iridoidy MeSH
- kolagen chemie ultrastruktura MeSH
- lidé MeSH
- mikroskopie fluorescenční multifotonová MeSH
- perikard chemie transplantace ultrastruktura MeSH
- pevnost v tahu MeSH
- povrchová plasmonová rezonance MeSH
- reagencia zkříženě vázaná MeSH
- testování materiálů MeSH
- viabilita buněk MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biokompatibilní materiály * MeSH
- fibrin MeSH
- fibronektiny MeSH
- genipin MeSH Prohlížeč
- glutaraldehyd MeSH
- iridoidy MeSH
- kolagen MeSH
- reagencia zkříženě vázaná MeSH
Decellularized human pericardium is under study as an allogenic material for cardiovascular applications. The effects of crosslinking on the mechanical properties of decellularized pericardium were determined with a uniaxial tensile test, and the effects of crosslinking on the collagen structure of decellularized pericardium were determined by multiphoton microscopy. The viability of human umbilical vein endothelial cells seeded on decellularized human pericardium and on pericardium strongly and weakly crosslinked with glutaraldehyde and with genipin was evaluated by means of an MTS assay. The viability of the cells, measured by their metabolic activity, decreased considerably when the pericardium was crosslinked with glutaraldehyde. Conversely, the cell viability increased when the pericardium was crosslinked with genipin. Coating both non-modified pericardium and crosslinked pericardium with a fibrin mesh or with a mesh containing attached heparin and/or fibronectin led to a significant increase in cell viability. The highest degree of viability was attained for samples that were weakly crosslinked with genipin and modified by means of a fibrin and fibronectin coating. The results indicate a method by which in vivo endothelialization of human cardiac allografts or xenografts could potentially be encouraged.
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