Skip to main content

Research Repository

Advanced Search

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

In vitro degradation and mechanical properties of PLA-PCL copolymer unit cell scaffolds generated by two-photon polymerization Thumbnail


Authors

R. M. Felfel

Leander Poocza

Tobias Milde

Gerhard Hildebrand

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

Files





You might also like



Downloadable Citations