Premium
Tuning Mechanical Properties of Chondroitin Sulfate‐ B ased Double‐ N etwork Hydrogels
Author(s) -
Suekama Tiffany C.,
Hu Jian,
Kurokawa Takayuki,
Gong Jian Ping,
Gehrke Stevin H.
Publication year - 2013
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.201300012
Subject(s) - self healing hydrogels , materials science , toughness , ethylene glycol , acrylamide , copolymer , chondroitin sulfate , interpenetrating polymer network , modulus , polyacrylamide , chemical engineering , composite material , polymer , polymer chemistry , chemistry , biochemistry , glycosaminoglycan , engineering
Summary High strength double‐network (DN) biopolymer‐based hydrogels were created using copolymers of methacrylated chondroitin sulfate (MCS) and poly(ethylene glycol) diacrylate (PEGDA) as the first network and polyacrylamide (PAAm) as the second network. The concentration and cross‐linking of the networks were adjusted to control the mechanical properties including the failure stress, failure strain, Young's modulus, and yielding behavior. First, we increased the cross‐linking of the first network both by increasing the MCS concentration from 13 to 20 wt% and by copolymerizing MCS with 2 to 6 wt% PEGDA. The additional cross‐linking increased the Young's modulus as much as five times, reaching 3.3 MPa, and the failure stress up as much as four times, reaching 2.9 MPa. However, this also reduced failure strain from a high of 2.9 mm/mm to a low of 0.12 mm/mm and diminished the yielding region. Changes in the concentrations of acrylamide or its cross‐linking with N,N′‐methylenebisacrylamide (BIS) in the second network had a lesser effect on the DN properties. We hypothesized that to obtain a yielding region which results in high toughness, we need to alter the cross‐linking of the first network such that the yield stress of the MCS‐PEGDA/PAAm DN does not exceed the failure stress of PAAm network. Because of the wide range of mechanical properties achieved in these DNs with limited changes in the swelling degrees, unlike conventional single‐network gels, the DN approach allows attainment of a much greater range of mechanical behavior than is possible with single networks.