z-logo
open-access-imgOpen Access
Viscoelasticity of hydrazone crosslinked poly(ethylene glycol) hydrogels directs chondrocyte morphology during mechanical deformation
Author(s) -
Benjamin M. Richardson,
Cierra J. Walker,
Laura J. Macdougall,
Jack W. Hoye,
Mark A. Randolph,
Stephanie J. Bryant,
Kristi S. Anseth
Publication year - 2020
Publication title -
biomaterials science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.422
H-Index - 64
eISSN - 2047-4849
pISSN - 2047-4830
DOI - 10.1039/d0bm00860e
Subject(s) - self healing hydrogels , viscoelasticity , ethylene glycol , morphology (biology) , hydrazone , chondrocyte , polymer chemistry , chemistry , chemical engineering , biophysics , polymer science , materials science , composite material , organic chemistry , biochemistry , biology , in vitro , genetics , engineering
Chondrocyte deformation influences disease progression and tissue regeneration in load-bearing joints. In this work, we found that viscoelasticity of dynamic covalent crosslinks temporally modulates the biophysical transmission of physiologically relevant compressive strains to encapsulated chondrocytes. Chondrocytes in viscoelastic alky-hydrazone hydrogels demonstrated (91.4 ± 4.5%) recovery of native rounded morphologies during mechanical deformation, whereas primarily elastic benzyl-hydrazone hydrogels significantly limited morphological recovery (21.2 ± 1.4%).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom