Abstract
A Michael addition strategy involving the reaction between a maleimide double bond and amine groups is investigated for the synthesis of cryogels at subzero temperature. Low-molecular-weight PEG-based building blocks with amine end groups and disulfide-containing building blocks with maleimide end groups are combined to synthesize redox-responsive PEG cryogels. The cryogels exhibit an interconnected macroporous morphology, a high compressive modulus and gelation yields of around 95%. While the cryogels are stable under physiological conditions, complete dissolution of the cryogels into water-soluble products is obtained in the presence of a reducing agent (glutathione) in the medium. Cell seeding experiments and toxicologic analysis demonstrate their potential as scaffolds in tissue engineering. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Dispinar, T., Van Camp, W., De Cock, L. J., De Geest, B. G., & Du Prez, F. E. (2012). Redox-Responsive Degradable PEG Cryogels as Potential Cell Scaffolds in Tissue Engineering. Macromolecular Bioscience, 12(3), 383–394. https://doi.org/10.1002/mabi.201100396
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