Journal
RSC ADVANCES
Volume 6, Issue 21, Pages 17228-17238Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra25007b
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Funding
- National Science Foundation [NSF51103019, NSF21174027]
- National High-tech Research and Development Projects (863) [2012AA03A605]
- Program for New Century Excellent Talents in University [12X10623]
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A series of amphiphilic block copolymers containing hydrophobic polydimethylsiloxane (PDMS) segments and hydrophilic poly(N,N-dimethylacrylamide) (PDMAAm) segments have been synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization, which were then crosslinked into well-defined amphiphilic conetworks (APCNs) via ultraviolet (UV) induced thiol-ene click chemistry. Briefly, a PDMS-based RAFT agent was synthesized from the esterification of trithiocarbonate and bis(hydroxyethyloxypropyl) PDMS, and was used to control the RAFT polymerization of monomer DMAAm and allyl methacrylate (AMA) to form amphiphilic copolymers with a well-defined molecular mass and narrow dispersity. The amphiphilic copolymers were then crosslinked via UV induced thiol-ene click chemistry into APCNs, which showed unique amphiphilic characteristics as well as good mechanical properties, making them potential candidates in biomaterials. Transmission electron microscopy (TEM) and atomic force microscopy (AFM) inferred that the resultant APCN exhibited the behavior of microphase separation with a small channel size and uniform phase domain. Therefore, this kind of APCN possessed excellent comprehensive properties, i.e. a well-defined and co-continuous microstructure and high water uptake properties with a homogeneous hydrophilic channel, low cytotoxicity, high mechanical strength (2.1 +/- 0.7 MPa) and elongation ratio (173 +/- 17%), suggesting a promising biomaterial candidate for contact lenses, drug controlled systems, biomedical scaffolds for tissue engineering and supports for biocatalysts.
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