Back to Search Start Over

A nanostructured carbon-reinforced polyisobutylene-based thermoplastic elastomer.

Authors :
Puskas JE
Foreman-Orlowski EA
Lim GT
Porosky SE
Evancho-Chapman MM
Schmidt SP
El Fray M
Piatek M
Prowans P
Lovejoy K
Source :
Biomaterials [Biomaterials] 2010 Mar; Vol. 31 (9), pp. 2477-88. Date of Electronic Publication: 2009 Dec 24.
Publication Year :
2010

Abstract

This paper presents the synthesis and characterization of a polyisobutylene (PIB)-based nanostructured carbon-reinforced thermoplastic elastomer. This thermoplastic elastomer is based on a self-assembling block copolymer having a branched PIB core carrying -OH functional groups at each branch point, flanked by blocks of poly(isobutylene-co-para-methylstyrene). The block copolymer has thermolabile physical crosslinks and can be processed as a plastic, yet retains its rubbery properties at room temperature. The carbon-reinforced thermoplastic elastomer had more than twice the tensile strength of the neat polymer, exceeding the strength of medical grade silicone rubber, while remaining significantly softer. The carbon-reinforced thermoplastic elastomer displayed a high T(g) of 126 degrees C, rendering the material steam-sterilizable. The carbon also acted as a free radical trap, increasing the onset temperature of thermal decomposition in the neat polymer from 256.6 degrees C to 327.7 degrees C. The carbon-reinforced thermoplastic elastomer had the lowest water contact angle at 82 degrees and surface nano-topography. After 180 days of implantation into rabbit soft tissues, the carbon-reinforced thermoplastic elastomer had the thinnest tissue capsule around the microdumbbell specimens, with no eosinophiles present. The material also showed excellent integration into bones.<br /> (Copyright 2009 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-5905
Volume :
31
Issue :
9
Database :
MEDLINE
Journal :
Biomaterials
Publication Type :
Academic Journal
Accession number :
20034664
Full Text :
https://doi.org/10.1016/j.biomaterials.2009.12.003