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Cholesterol-modified superporous poly(2-hydroxyethyl methacrylate) scaffolds for tissue engineering

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    0330578 - ÚEM 2010 RIV GB eng J - Journal Article
    Kubinová, Šárka - Horák, Daniel - Syková, Eva
    Cholesterol-modified superporous poly(2-hydroxyethyl methacrylate) scaffolds for tissue engineering.
    [Cholesterolem modifikovaný superporezní poly(2-hydroxyethyl methacrylátový konstrukt pro tkáňové inženýrství.]
    Biomaterials. Roč. 30, č. 27 (2009), s. 4601-4609. ISSN 0142-9612. E-ISSN 1878-5905
    R&D Projects: GA AV ČR KAN200520804
    Grant - others:EC FP6(XE) LSHM-CT-2007-037862
    Institutional research plan: CEZ:AV0Z50390512; CEZ:AV0Z40500505
    Keywords : cell adhesion * cell viability * hydrogel
    Subject RIV: FH - Neurology
    Impact factor: 7.365, year: 2009

    Modifications of poly(2-hydroxyethyl methacrylate) (PHEMA) with cholesterol and laminin have been developed to design scaffolds that promote cell–surface interaction. Cholesterol- (P(HEMA–CHLMA)) and laminin-modified (LN–PHEMA) superporous PHEMA scaffolds have been prepared by the bulk radical copolymerization of 2-hydroxyethyl methacrylate (HEMA), cholesterol methacrylate (CHLMA) and the cross-linking agent ethylene imethacrylate in the presence of ammonium oxalate crystals to introduce interconnected superpores in the matrix. Neat PHEMA and laminin-modified PHEMA scaffolds facilitated MSC attachment, but did not support cell spreading and proliferation; the viability of the attached cells decreased with time of cultivation. In contrast, MSCs spread and proliferated on P(HEMA–CHLMA) and LN-P(HEMA–CHLMA) hydrogels.

    Modifikace poly(2-hydroxyethyl methacrylátu) (PHEMA) cholesterolem a lamininem byla použita k tvorbě hydrogelu, který umožňuje buněčnou adhezi. Cholesterolem (P(HEMA–CHLMA) a lamininem (LN–PHEMA) modifikovaný porézní PHEMA konstrukt byl připraven radikálovou kopolymerizací 2-hydroxyethyl methacrylátu (HEMA), cholesterol methacrylátu (CHLMA) a síťovacího činidla ethylen imethacrylátu v přítomnosti krystalů oxalátu ammonia umožňují tvorbu propojených pórů v matrici. MSCs se zachytily na povrch nemodifikovaných PHEMA a LN-PHEMA hydrogelů, ale nedošlo k jejich adhezi a proliferaci a jejich životnost během kultivace klesala. Naproti tomu, MSCs adherovaly a proliferovaly na P(HEMA–CHLMA) a LN-P(HEMA–CHLMA) hydrogelech.
    Permanent Link: http://hdl.handle.net/11104/0005480

     
     
Number of the records: 1  

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