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dc.contributor.authorBarnes, A.L.*
dc.contributor.authorGenever, P.G.*
dc.contributor.authorRimmer, Stephen*
dc.contributor.authorColes, M.C.*
dc.date.accessioned2017-02-15T15:02:34Z
dc.date.available2017-02-15T15:02:34Z
dc.date.issued2016
dc.identifier.citationBarnes AL, Genever PG, Rimmer S et al (2016) Biomacromolecules (2016) Collagen–Poly(N-isopropylacrylamide) Hydrogels with Tunable Properties. Biomacromolecules. 17(3): 723-734.
dc.identifier.urihttp://hdl.handle.net/10454/11369
dc.descriptionNo
dc.description.abstractThere is a lack of hydrogel materials whose properties can be tuned at the point of use. Biological hydrogels, such as collagen, gelate at physiological temperatures; however, they are not always ideal as scaffolds because of their low mechanical strength. Their mechanics can be improved through cross-linking and chemical modification, but these methods still require further synthesis. We have demonstrated that by combining collagen with a thermoresponsive polymer, poly(N-isopropylacrylamide) (PNIPAM), the mechanical properties can be improved while maintaining cytocompatibility. Furthermore, different concentrations of this polymer led to a range of hydrogels with shear moduli ranging from 105 Pa down to less than 102 Pa, similar to the soft tissues in the body. In addition to variable mechanical properties, the hydrogel blends have a range of micron-scale structures and porosities, which caused adipose-derived stromal cells (ADSCs) to adopt different morphologies when encapsulated within and may therefore be able to direct cell fate.
dc.description.sponsorshipEPSRC
dc.language.isoen
dc.subjectHydrogel
dc.subjectCollagen
dc.titleCollagen–Poly(N-isopropylacrylamide) Hydrogels with Tunable Properties
dc.status.refereedYes
dc.date.application2015-12-19
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1021/acs.biomac.5b01251
dc.openaccess.statusclosedAccess


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