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Post-self-assembly experimentation on extruded collagen fibres for tissue engineering applications
Extruded collagen fibres have been shown to constitute a biomimetic three-dimensional scaffold with numerous tissue engineering applications. The multi-step fabrication process of this material provides opportunities for further advancements to improve the properties of the final product. Herein we...
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Published in: | Acta biomaterialia 2008-11, Vol.4 (6), p.1646-1656 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Extruded collagen fibres have been shown to constitute a biomimetic three-dimensional scaffold with numerous tissue engineering applications. The multi-step fabrication process of this material provides opportunities for further advancements to improve the properties of the final product. Herein we investigated the influence of the post-self-assembly washing baths on the structural, mechanical and thermal properties of these fibres. The surface morphology and the inter-fibre packing were similar for every treatment. The overnight incubation in isopropanol yielded fibres with the highest temperature and energy of denaturation (
p
<
0.013). Typical s- and j-shape stress–strain curves were obtained for all treatments in the dry and wet state respectively. Rehydration of the fibres resulted in increased fibre diameter (
p
<
0.006) and reduced stress (
p
<
0.001), force (
p
<
0.001) and modulus (
p
<
0.002) values for every treatment. In the dry state, the alcohol-treated fibres were characterized by the highest stress (
p
<
0.002) values; whilst in the wet state the Tris–HCl-treated fibres were the weakest (
p
<
0.006). For every treatment, in both dry and wet state, a strong and inverse relationship between the fibre diameter and the stress at break was observed. Overall, the fibres produced were characterized by properties similar to those of native tissues. |
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ISSN: | 1742-7061 1878-7568 |
DOI: | 10.1016/j.actbio.2008.05.015 |