| Literature DB >> 24530853 |
Israel González de Torre1, Mercedes Santos2, Luis Quintanilla2, Ana Testera2, Matilde Alonso2, José Carlos Rodríguez Cabello2.
Abstract
Elastin-like recombinamer catalyst-free click gels (ELR-CFCGs) have been prepared and characterized by modifying both a structural ELR (VKVx24) and a biofunctionalized ELR-bearing RGD cell-adhesion sequence (HRGD6) to bear the reactive groups needed to form hydrogels via a click reaction. Prior to formation of the ELR-CFCGs, azide-bearing and cyclooctyne-modified ELRs were also synthesized. Subsequent covalent crosslinking was based on the reaction between these azide and cyclooctyne groups, which takes place under physiological conditions and without the need for a catalyst. The correlation among SEM micrographs, porosity, swelling ratio, and rheological measurements have been carried out. The storage and loss moduli at 1Hz are in the range 1-10kPa and 100-1000Pa, respectively. The linear dependence of |G∗| on f(½) and the peak value of tan δ were considered to be consistent with a poroelastic mechanism dominating the frequency range 0.3-70Hz. The discrete relaxation spectrum was obtained from stress relaxation measurements (t>5s). The good fit of the relaxation modulus to decrease exponential functions suggests that an intrinsic viscoelastic mechanism dominates the transients. Several recombinamer concentrations and temperatures were tested to obtain gels with fully tuneable properties that could find applications in the biomedical field.Entities:
Keywords: Catalyst-free click chemistry; ELRs; Fluid-independent viscoelasticity; Poroelasticity
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Year: 2014 PMID: 24530853 DOI: 10.1016/j.actbio.2014.02.006
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947