Diepoxide-triggered conformational transition of silk fibroin: formation of hydrogels.

Abstract:

:Silk fibroin hydrogels with tunable properties could be obtained from aqueous fibroin solutions (4.2 w/v %) in a short period of time. This was achieved by the addition of ethylene glycol diglycidyl ether (EGDE) into the reaction solution. Introduction of EGDE cross-links between the fibroin molecules decreases the mobility of the chains, which triggers the conformational transition from random-coil to β-sheet structure and hence fibroin gelation. Dynamic rheological measurements conducted at 50 °C show the formation of strong to weak hydrogels depending on the pH of the reaction solution. Although EGDE attacks the amino groups of fibroin and forms interstrand cross-links, β-sheets acting as physical cross-links dominate the elasticity of the hydrogels. Mechanical response of low-modulus fibroin hydrogels formed above pH 9.7 is highly nonlinear with strong strain hardening behavior (700%) arising from the alignment of the crystallizable amino acid segments.

journal_name

Biomacromolecules

journal_title

Biomacromolecules

authors

Karakutuk I,Ak F,Okay O

doi

10.1021/bm300006r

subject

Has Abstract

pub_date

2012-04-09 00:00:00

pages

1122-8

issue

4

eissn

1525-7797

issn

1526-4602

journal_volume

13

pub_type

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