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Arrays of polyacrylamide hydrogels using a carbodiimide-mediated crosslinking reaction

Citation

Sheng, Q and Tian, W and Lapierre, F and Gao, S and Mulder, RJ and Zhu, Y and Kozielski, KA and Wood, CD, Arrays of polyacrylamide hydrogels using a carbodiimide-mediated crosslinking reaction, Journal of Applied Polymer Science, 131, (12) Article 40416. ISSN 0021-8995 (2014) [Refereed Article]

Copyright Statement

Copyright 2014 Wiley Periodicals, Inc.

Official URL: http://dx.doi.org/10.1002/app.40416

DOI: doi:10.1002/APP.40416

Abstract

This study introduces a radical-free approach for generating polyacrylamide (PAM) hydrogels with no toxic residues remaining in the networks. Acrylamide and bisacrylamide, which are neurotoxins, are not used during the hydrogel synthesis and only nontoxic side products are generated. This is achieved using a gentle carbodiimide-mediated crosslinking (CMCL) reaction that does not require complex initiation systems and is effective in the presence of oxygen. This overcomes some of the key limitations related to PAM hydrogel synthesis using free-radical routes and maintains the advantages of synthetic hydrogels over biopolymers. In addition, the CMCL reaction allows for accurate placement of functional groups, which controls hydrogel structure and performance including mechanical strength, swelling capacity, and hydrophobic balance. This flexibility is demonstrated through the synthesis and rheological characterization of a library of structurally diverse hydrogels as well as spherical hydrogels. PAM-based hydrogels are used extensively in a broad number of applications, and this study demonstrates the applicability of this method as a nontoxic and radical-free complementary alternative route that can generate structures analogous to those prepared using free-radical routes.

Item Details

Item Type:Refereed Article
Keywords:gels, microfluidics, microgels, rheology, crosslinking
Research Division:Technology
Research Group:Environmental Biotechnology
Research Field:Biodiscovery
Objective Division:Manufacturing
Objective Group:Industrial Chemicals and Related Products
Objective Field:Soaps and Cosmetics
Author:Lapierre, F (Dr Florian Lapierre)
ID Code:99982
Year Published:2014
Web of Science® Times Cited:5
Deposited By:Austn Centre for Research in Separation Science
Deposited On:2015-04-22
Last Modified:2017-11-03
Downloads:0

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