Published November 9, 2010 | Version Accepted Version + Supplemental Material
Journal Article Open

Yielding Behavior in Injectable Hydrogels from Telechelic Proteins

  • 1. ROR icon California Institute of Technology

Abstract

Injectable hydrogels show substantial promise for use in minimally invasive tissue engineering and drug delivery procedures. A new injectable hydrogel material, developed from recombinant telechelic proteins expressed in E. coli, demonstrates shear thinning by 3 orders of magnitude at large strains. Large-amplitude oscillatory shear illustrates that shear thinning is due to yielding within the bulk of the gel, and the rheological response and flow profiles are consistent with a shear-banding mechanism for yielding. The sharp yielding transition and large magnitude of the apparent shear thinning allow gels to be injected through narrow gauge needles with only gentle hand pressure. After injection the gels reset to full elastic strength in seconds due to rapid re-formation of the physical network junctions, allowing self-supporting structures to be formed. The shear thinning and recovery behavior is largely independent of the midblock length, enabling genetic engineering to be used to control the equilibrium modulus of the gel without loss of the characteristic yielding behavior. The shear-banding mechanism localizes deformation during flow into narrow regions of the gels, allowing more than 95% of seeded cells to survive the injection process.

Additional Information

© 2010 American Chemical Society. Received June 28, 2010; Revised Manuscript Received September 27, 2010. Published on Web 10/13/2010. This work was supported by the NSF Center for the Science and Engineering of Materials and NIH Grant EB1971. B.D.O. was supported by Award F32GM0834 from the National Institute of General Medical Sciences and by a Beckman Institute Postdoctoral Fellowship. We thank Professor S. E. Fraser for suggesting the method of flow visualization reported in Figure 3.

Attached Files

Accepted Version - nihms245292.pdf

Supplemental Material - ma101434a_si_001.pdf

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Additional details

Identifiers

PMCID
PMC3017468
Eprint ID
21204
Resolver ID
CaltechAUTHORS:20101207-081608961

Funding

NSF
NIH
EB1971
NIH Postdoctoral Fellowship
F32GM0834
Caltech Beckman Institute

Dates

Created
2010-12-14
Created from EPrint's datestamp field
Updated
2021-11-09
Created from EPrint's last_modified field