Variably Elastic Hydrogel Patterned via Capillary Action in Microchannels

Rui Dong, Tor W. Jensen, Kristin Engberg,§ Ralph G. Nuzzo, and Deborah E. Leckband*§
Department of Chemistry, Institute for Genomic Biology, and Department of Chemical and Biomolecular Engineering, University of Illinois, Urbana-Champaign, Illinois 61801
Langmuir, 2007, 23 (3), pp 1483–1488
DOI: 10.1021/la062738l
Publication Date (Web): December 5, 2006
Copyright © 2007 American Chemical Society

 Department of Chemistry.

,

 Rui Dong and Tor Jensen have contributed equally to this work.

,

 Institute for Genomic Biology.

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§

 Department of Chemical & Biomolecular Engineering.

,

 Current address:  Department of Chemical Engineering, Stanford University, Palo Alto, CA.

,
*

 To whom correspondence should be addressed:  leckband@uiuc.edu.

Abstract

Abstract Image

Agarose hydrogels of varied elastic modulus can be patterned into 100-μm-wide channels with wall heights of 60 μm. After modifying the hydrogels with chloroacetic acid (acid gels), they are amenable to modification with amine-containing ligands using EDC-NHS chemistry. Using both rheometry and atomic force microscopy (AFM) nanoindentation measurements, the elastic modulus of unmodified hydrogels increases linearly from 3.6 ± 0.5 kPa to 45.2 ± 5.5 kPa for 0.5 to 2.0 wt/vol % hydrogel, respectively. The elastic modulus of acid gels is 2.2 ± 0.3 kPa to 16.2 ± 1.6 kPa for 0.5 to 2.0wt/vol %, respectively. No further changes were measured after further modifying the acid gels with fibronectin. Confocal images of rhodamine-modified acid gels show that the optimal filling viscosity of the agarose solutions is between 1 and 4 cP. This new method of patterning allows for the creation of substrates that take advantage of both micron-scale patterns and variably elastic hydrogels.

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History

  • Published In Issue January 30, 2007
  • Received September 19, 2006

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