Effect of crosslinked poly (1-vinyl-2-pyrrolidinone) gels on cell growth in static cell cultures

YE Hong, TV Chirila, JH Fitton… - Bio-Medical …, 1997 - content.iospress.com
YE Hong, TV Chirila, JH Fitton, BW Ziegelaar, IJ Constable
Bio-Medical Materials and Engineering, 1997content.iospress.com
Abstract Poly (1-vinyl-2-pyrrolidinone)(PVP) and copolymers of 1-vinyl-2-pyrrolidinone are
insoluble in water when crosslinked but they can absorb very large amounts of water to
become syringe-injectable hydrogels. Such gels have been investigated recently as
potential substitutes for the vitreous humour in the eye. In this study, during the cytotoxic
evaluation by sulforhodamine B colorimetric assay of variously crosslinked PVP gels, it was
found that many of them showed protective/growth promoting effects on 3T3 mouse …
Abstract
Poly (1-vinyl-2-pyrrolidinone)(PVP) and copolymers of 1-vinyl-2-pyrrolidinone are insoluble in water when crosslinked but they can absorb very large amounts of water to become syringe-injectable hydrogels. Such gels have been investigated recently as potential substitutes for the vitreous humour in the eye. In this study, during the cytotoxic evaluation by sulforhodamine B colorimetric assay of variously crosslinked PVP gels, it was found that many of them showed protective/growth promoting effects on 3T3 mouse fibroblasts in static cultures, a phenomenon encountered previously only with aqueous solutions of a limited number of natural or synthetic polymers. Particularly, the gels crosslinked with diethylene glycol dimethacrylate (DEGDMA) induced a significant enhancement of cell proliferation, especially in serum-free cultures. No correlation between this effect and the essential gel properties (chemical composition, viscoelasticity and equilibrium water content) could be established. The study demonstrated that crosslinked PVP hydrogels showed a serum-like growth promoting effect on an anchorage-dependent cell line, which may be due to physical protection, inability of the insoluble gels to penetrate cell membranes, and their ability to mimic the extracellular matrix.
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