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Article Citation - WoS: 17Citation - Scopus: 18Poly(ε-Caprolactone) Composites Containing Gentamicin-Loaded Β-Tricalcium Phosphate/Gelatin Microspheres as Bone Tissue Supports(Wiley, 2013) Sezer, Umran Aydemir; Aksoy, Eda Ayse; Hasirci, Vasif; Hasirci, NesrinIn this work, novel antibacterial composites were prepared by using poly(epsilon-caprolactone) (PCL) as the main matrix material, and gentamicin-loaded microspheres composed of beta-tricalcium phosphate (beta-TCP) and gelatin. The purpose is to use this biodegradable material as a support for bone tissue. This composite system is expected to enhance bone regeneration by the presence of beta-TCP and prevent a possible infection that might occur around the defected bone region by the release of gentamicin. The effects of the ratio of the beta-TCP/gelatin microspheres on the morphological, mechanical, and degradation properties of composite films as well as in vitro antibiotic release and antibacterial activities against Escherichia coli and Staphylococcus aureus were investigated. The results showed that the composites of PCL and beta-TCP/gelatin microspheres had antibacterial activities for both bacteria. (C) 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013Article Citation - WoS: 7Citation - Scopus: 9Semi-Ipn Chitosan/Polyvinylpyrrolidone Microspheres and Films: Sustained Release and Property Optimisation(Taylor & Francis Ltd, 2013) Ozerkan, Taylan; Sezer, Umran Aydemir; Gurhan, Ismet Deliloglu; Iz, Sultan Gulce; Hasirci, NesrinA set of chitosan-polyvinylpyrrolidone (CH-PVP) microspheres were prepared as semi-inter penetrating networks (semi-IPN) and loaded with 5-fluorouracil. In vitro release studies showed faster release for semi-IPN microspheres compared to pure CH samples, and the total release was achieved in about 20-30 days, depending on the composition. In vitro cell studies were achieved against human breast adenocarcinoma cell line cells where adsorption of cells on microspheres with a significant decrease in their number was obtained. Meanwhile, the CH-PVP films, which were prepared with the same compositions as in the microspheres, demonstrated an increase in strength from 66 to 118 MPa as the PVP content was decreased. It can be concluded that the prepared CH-PVP semi-IPN microspheres are novel promising carriers compared to pure CH microspheres since it becomes possible to adjust stability and hydrophilicity of the microspheres as well as the release rates of the drugs from the microspheres by changing the ratio of CH/PVP composition.
