R. M. Felfel
In vitro degradation and mechanical properties of PLA-PCL copolymer unit cell scaffolds generated by two-photon polymerization
Felfel, R. M.; Poocza, Leander; Gimeno-Fabra, Miquel; Milde, Tobias; Hildebrand, Gerhard; Ahmed, Ifty; Scotchford, Colin; Sottile, Virginie; Grant, David M.; Liefeith, Klaus
Authors
Leander Poocza
MIQUEL GIMENO-FABRA M.Gimeno-Fabra@nottingham.ac.uk
Assistant Professor in Mechanical Engineering
Tobias Milde
Gerhard Hildebrand
Associate Professor IFTY AHMED ifty.ahmed@nottingham.ac.uk
Professor of Materials Science and Engineering
COLIN SCOTCHFORD COLIN.SCOTCHFORD@NOTTINGHAM.AC.UK
Associate Professor
Virginie Sottile
DAVID GRANT DAVID.GRANT@NOTTINGHAM.AC.UK
Professor of Materials Science
Klaus Liefeith
Abstract
© 2016 IOP Publishing Ltd. The manufacture of 3D scaffolds with specific controlled porous architecture, defined microstructure and an adjustable degradation profile was achieved using two-photon polymerization (TPP) with a size of 2 × 4 × 2 mm3. Scaffolds made from poly(D,L-lactide-co-ε-caprolactone) copolymer with varying lactic acid (LA) and ε -caprolactone (CL) ratios (LC16:4, 18:2 and 9:1) were generated via ring-opening-polymerization and photoactivation. The reactivity was quantified using photo-DSC, yielding a double bond conversion ranging from 70% to 90%. The pore sizes for all LC scaffolds were see 300 μm and throat sizes varied from 152 to 177 μm. In vitro degradation was conducted at different temperatures; 37, 50 and 65°C. Change in compressive properties immersed at 37°C over time was also measured. Variations in thermal, degradation and mechanical properties of the LC scaffolds were related to the LA/CL ratio. Scaffold LC16:4 showed significantly lower glass transition temperature (T g) (4.8°C) in comparison with the LC 18:2 and 9:1 (see 32°C). Rates of mass loss for the LC16:4 scaffolds at all temperatures were significantly lower than that for LC18:2 and 9:1. The degradation activation energies for scaffold materials ranged from 82.7 to 94.9 kJ mol-1. A prediction for degradation time was applied through a correlation between long-term degradation studies at 37°C and short-term studies at elevated temperatures (50 and 65°C) using the half-life of mass loss (Time (M1/2)) parameter. However, the initial compressive moduli for LC18:2 and 9:1 scaffolds were 7 to 14 times higher than LC16:4 (see 0.27) which was suggested to be due to its higher CL content (20%). All scaffolds showed a gradual loss in their compressive strength and modulus over time as a result of progressive mass loss over time. The manufacturing process utilized and the scaffolds produced have potential for use in tissue engineering and regenerative medicine applications.
Citation
Felfel, R. M., Poocza, L., Gimeno-Fabra, M., Milde, T., Hildebrand, G., Ahmed, I., …Liefeith, K. (2016). In vitro degradation and mechanical properties of PLA-PCL copolymer unit cell scaffolds generated by two-photon polymerization. Biomedical Materials, 11(1), Article 015011. https://doi.org/10.1088/1748-6041/11/1/015011
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 1, 2015 |
Online Publication Date | Feb 2, 2016 |
Publication Date | Feb 2, 2016 |
Deposit Date | Jun 28, 2016 |
Publicly Available Date | Jun 28, 2016 |
Journal | Biomedical Materials (Bristol) |
Print ISSN | 1748-6041 |
Electronic ISSN | 1748-605X |
Publisher | IOP Publishing |
Peer Reviewed | Peer Reviewed |
Volume | 11 |
Issue | 1 |
Article Number | 015011 |
DOI | https://doi.org/10.1088/1748-6041/11/1/015011 |
Keywords | scaffolds, stereo-lithography, photopolymerization, conversion, degradation, activation energy, compressive properties |
Public URL | https://nottingham-repository.worktribe.com/output/777379 |
Publisher URL | http://iopscience.iop.org/article/10.1088/1748-6041/11/1/015011/meta |
Additional Information | This is an author-created, un-copyedited version of an article accepted for publication in Biomedical Materials. The publisher is not responsible for any errors or missions in this version of the manuscript or any version derived from it. The Version of Record is available online at doi:10.1088/1748-6041/11/1/015011. |
Contract Date | Jun 28, 2016 |
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