## Abstract Aliphatic segmented poly(ester amide)s, comprising a crystallizable amide phase and a flexible amorphous ester phase, were investigated for potential use in biomedical applications. By varying the amide content and the type of crystallizable amide segments, the polymer's thermal and mec
In vitro degradation and in vivo biocompatibility study of a new linear poly(urethane urea)
✍ Scribed by Basse Asplund; Cecilia Aulin; Tim Bowden; Niklas Eriksson; Torbjörn Mathisen; Lars-Magnus Bjursten; Jöns Hilborn
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 447 KB
- Volume
- 86B
- Category
- Article
- ISSN
- 1552-4973
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✦ Synopsis
Abstract
Segmented poly(urethane urea)s (PUUs) with hard segments derived only from methyl 2,6‐diisocyantohexanoate (LDI) without the use of a chain extender have previously been described. These materials, which contain hard segments with multiple urea linkages, show exceptionally high strain capability (1600–4700%). In the study reported here, the rate and effect of hydrolysis of these materials were determined for gamma‐sterilized and nonsterilized samples. Materials investigated contained PCL, PTMC, P(TMC‐co‐CL), P(CL‐co‐DLLA), or P(TMC‐co‐DLLA) as soft segments and, as well as their mechanical properties, changes in mass, inherent viscosity (I.V.), and thermal properties were studied over 20 weeks. Results showed that the degradation rate was dependant on the soft segment structure, with a higher rate of degradation for the polyester‐dominating PUUs exhibiting a substantial loss in I.V. A tendency of reduction of tensile strength and strain hardening was seen for all samples. Also, loss in elongation at break was detected, for PUU‐P(CL‐DLLA) it went from 1600% to 830% in 10 weeks. Gamma radiation caused an initial loss in I.V. and induced more rapid hydrolysis compared with nonsterilized samples, except for PUU‐PTMC. A cytotoxicity test using human fibroblasts demonstrated that the material supports cell viability. In addition, an in vivo biocompatibility study showed a typical foreign body reaction after 1 and 6 weeks. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008
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