Duplicating Dynamic Strain-Stiffening Behavior and Nanomechanics of Biological Tissues in a Synthetic Self-Healing Flexible Network Hydrogel

ACS Nano. 2017 Nov 28;11(11):11074-11081. doi: 10.1021/acsnano.7b05109. Epub 2017 Oct 2.

Abstract

Biological tissues can accurately differentiate external mechanical stresses and actively select suitable strategies (e.g., reversible strain-stiffening, self-healing) to sustain or restore their integrity and related functionalities as required. Synthetic materials that can imitate the characteristics of biological tissues have a wide range of engineering and bioengineering applications. However, no success has been demonstrated to realize such strain-stiffening behavior in synthetic networks, particularly using flexible polymers, which has remained a great challenge. Here, we present one such synthetic hydrogel material prepared from two flexible polymers (polyethylene glycol and branched polyethylenimine) that exhibits both strain-stiffening and self-healing capabilities. The developed synthetic hydrogel network not only mimics the main features of biological mechanically responsive systems but also autonomously self-heals after becoming damaged, thereby recovering its full capacity to perform its normal physiological functions.

Keywords: dynamical covalent bonds; flexible network; hydrogel; self-healing; strain-stiffening.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Humans
  • Hydrogels / chemical synthesis
  • Hydrogels / chemistry*
  • Hydrogels / therapeutic use
  • Polyethylene Glycols / chemical synthesis
  • Polyethylene Glycols / chemistry
  • Polyethyleneimine / chemical synthesis
  • Polyethyleneimine / chemistry
  • Polymers / chemical synthesis
  • Polymers / chemistry*
  • Polymers / therapeutic use
  • Stress, Mechanical
  • Tissue Engineering*

Substances

  • Hydrogels
  • Polymers
  • Polyethylene Glycols
  • Polyethyleneimine