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Title:
Covalently linked biocompatible graphene/polycaprolactone composites for tissue engineering
Date:
2/2013
Link to Journal Abstract
Abstract:
Two synthesis routes to graphene/polycaprolactone composites are introduced and the properties of the resulting composites compared. In the first method, mixtures are produced using solution processing of polycaprolactone and well dispersed, chemically reduced graphene oxide and in the second, an esterification reaction covalently links polycaprolactone chains to free carboxyl groups on the graphene sheets. This is achieved through the use of a stable anhydrous dimethylformamide dispersion of graphene that has been highly chemically reduced resulting in mostly peripheral ester linkages. The resulting covalently linked composites exhibit far better homogeneity and as a result, both Young¡¯s modulus and tensile strength more than double and electrical conductivities increase by ¡Ö 14 orders of magnitude over the pristine polymer at less than 10% graphene content. In vitro cytotoxicity testing of the materials showed good biocompatibility resulting in promising materials for use as conducting substrates for the electrically stimulated growth of cells.
Non-technical Summary:
For this study, two synthesis routes to graphene/polycaprolactone composites are introduced and the properties of the resulting composites compared. In vitro cytotoxicity testing of the materials showed good biocompatibility resulting in promising materials for use as conducting substrates for the electrically stimulated growth of cells.
Content Emphasis
Peer Reviewed Journal Article
Exposure Or Hazard Target
Mammalian
Exposure Pathway
Other/Unspecified
Method Of Study
In Vitro
Paper Type
Hazard
Particle Type
Carbon
Production Method
Engineered
Risk Exposure Group
General Population
Target Audience
Technical Research
Citation:
Carbon, 52: 296-304 (February 2013)
Publication:
Carbon
Author:
Sayyar S, Murray E, Thompson BC, Gambhir S, Officer DL, Wallace GG
Volume:
52
Pages:
296-304
Last updated on March 18, 2013
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This work is supported in part by the Nanoscale Science and Engineering Initiative of the National Science Foundation
under NSF Award Number EEC-0118007.
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