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Article type: Research Article
Authors: Şaşmazel, Hilal Türkoğlu | Gümüşderelioğlu, Menemşe; | Gürpınar, Aylin | Onur, Mehmet Ali
Affiliations: Department of Materials Engineering, Atılım University, Ankara, Turkey | Chemical Engineering and Bioengineering Departments, Hacettepe University, Ankara, Turkey | Department of Biology, Hacettepe University, Ankara, Turkey
Note: [] Address for correspondence: Dr. M. Gümüşderelioğlu, Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey. Tel.: + 90-312-2977447; Fax: + 90-312-2992124; E-mail: menemse@hacettepe.edu.tr.
Abstract: In this contribution, PCL (poly-ε caprolactone) scaffolds were prepared by solvent-casting/particle-leaching technique in the presence of two pore formers, PEG4000 or sucrose molecules in different quantities (0, 10, 20, 30, 40, 50, 55 w/w% PEG4000/PCL; 10, 20 w/w% Sucrose/PCL). The surface and bulk properties of the resulting scaffolds were studied by SEM, DSC and FTIR. SEM photographs showed that, macroporosity was obtained in the PCL structures prepared with sucrose crystals while microporous structure was obtained in the presence of PEG4000 molecules. Average pore diameters calculated from SEM photographs were 40.1 and 191.2 μm for 40% PEG4000/PCL and 10% Sucrose/PCL scaffolds, respectively. The DSC and FTIR results confirmed that there is no any interaction between pore formers and PCL during structural formation, and both pore formers, PEG4000 and sucrose, remained independently in the scaffolds. L929 mouse fibroblast cells were seeded onto PCL structures and maintained during 7 days to evaluate cell proliferation. Cell culture results showed that, 10% Sucrose/PCL scaffold was the most promising substrate for L929 cell growth due to 3-D architecture and macroporous structure of the scaffold.
Keywords: Poly(ε-caprolactone), poly(ethylene glycol), sucrose, porous structures, L929 mouse fibroblasts, tissue engineering
DOI: 10.3233/BME-2008-0515
Journal: Bio-Medical Materials and Engineering, vol. 18, no. 3, pp. 119-128, 2008
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