Literature DB >> 21520481

Direct synthesis of biodegradable polysaccharide derivative hydrogels through aqueous Diels-Alder chemistry.

Huaping Tan1, J Peter Rubin, Kacey G Marra.   

Abstract

A robust synthetic strategy where polysaccharide derivative precursors react through aqueous Diels-Alder chemistry without the involvement of catalysts and coupling reagents, allowing for the direct encapsulation of positive and negative proteins within biodegradable hydrogels. The results demonstrated that the aqueous Diels-Alder chemistry provides an extremely selective reaction and proceeds with high efficiency for polysaccharide bioconjugation. This synthetic approach uniquely allows for the direct fabrication of biologically functionalized gels with ideal structures, which provides a competitive alternative to conventional conjugation techniques such as click chemistry.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2011        PMID: 21520481     DOI: 10.1002/marc.201100125

Source DB:  PubMed          Journal:  Macromol Rapid Commun        ISSN: 1022-1336            Impact factor:   5.734


  12 in total

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6.  Rapid Diels-Alder Cross-linking of Cell Encapsulating Hydrogels.

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Review 7.  Soft Materials by Design: Unconventional Polymer Networks Give Extreme Properties.

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Review 8.  Chemically Modified Biopolymers for the Formation of Biomedical Hydrogels.

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Review 9.  Alginate-Based Biomaterials for Regenerative Medicine Applications.

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Journal:  Materials (Basel)       Date:  2013-03-26       Impact factor: 3.623

Review 10.  Alginate-based hydrogels as drug delivery vehicles in cancer treatment and their applications in wound dressing and 3D bioprinting.

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