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Article Citation - WoS: 124Citation - Scopus: 129Novel Poly(ε-caprolactone)/Gelatin Wound Dressings Prepared by Emulsion Electrospinning With Controlled Release Capacity of Ketoprofen Anti-Inflammatory Drug(Elsevier, 2017) Basar, A. O.; Castro, S.; Torres-Giner, S.; Lagaron, J. M.; Sasmazel, H. TurkogluIn the present study, a single and binary Ketoprofen-loaded mats of ultrathin fibers were developed by electrospinning and their physical properties and drug release capacity was analyzed. The single mat was prepared by solution electrospinning of poly(e-caprolactone) (PCL) with Ketoprofen at a weight ratio of 5 wt%. This Ketoprofen-containing PCL solution was also used as the oil phase in a 7:3 (wt/wt) emulsion with gelatin dissolved in acidified water. The resultant stable oil-in-water (O/W) emulsion of PCL-in-gelatin, also containing Ketoprofen at 5 wt%, was electrospun to produce the binary mat. Cross-linking process was performed by means of glutaraldehyde vapor on the electrospun binary mat to prevent dissolution of the hydrophilic gelatin phase. The performed characterization indicated that Ketoprofen was successfully embedded in the single and binary electrospun mats, i.e. PCL and PCL/gelatin, and both mats showed high hydrophobicity but poor thermal resistance. In vitro release studies interestingly revealed that, in comparison to the single PCL electrospun mat, the binary PCL/gelatin mat significantly hindered Ketoprofen burst release and exhibited a sustained release capacity of the drug for up to 4 days. In addition, the electrospun Ketoprofen-loaded mats showed enhanced attachment and proliferation of L929 mouse fibroblast cells, presenting the binary mat the highest cell growth yield due to its improved porosity. The here-developed electrospun materials clearly show a great deal of potential as novel wound dressings with an outstanding controlled capacity to release drugs.Article Citation - WoS: 45Citation - Scopus: 46Novel Hybrid Scaffolds for the Cultivation of Osteoblast Cells(Elsevier, 2011) Sasmazel, Hilal TurkogluIn this study, natural biodegradable polysaccharide, chitosan, and synthetic biodegradable polymer, poly(epsilon-caprolactone) (PCL) were used to prepare 3D, hybrid polymeric tissue scaffolds (PCL/chitosan blend and PCL/chitosan/PCL layer by layer scaffolds) by using the electrospinning technique. The hybrid scaffolds were developed through HA addition to accelerate osteoblast cell growth. Characteristic examinations of the scaffolds were performed by micrometer, SEM, contact angle measurement system, ATR-FTIR, tensile machine and swelling experiments. The thickness of all electrospun scaffolds was determined in the range of 0.010 +/- 0.001-0.012 +/- 0.002 mm. In order to optimize electrospinning processes, suitable bead-free and uniform scaffolds were selected by using SEM images. Blending of PCL with chitosan resulted in better hydrophilicity for the PCL/chitosan scaffolds. The characteristic peaks of PCL and chitosan in the blend and layer by layer nanofibers were observed. The PCL/chitosan/PCL layer by layer structure had higher elastic modulus and tensile strength values than both individual PCL and chitosan structures. The layer by layer scaffolds exhibited the PBS absorption values of 184.2; 197.2% which were higher than those of PCL scaffolds but lower than those of PCL/chitosan blend scaffolds. SaOs-2 osteosarcoma cell culture studies showed that the highest ALP activities belonged to novel PCL/chitosan/PCL layer by layer scaffolds meaning better cell differentiation on the surfaces. (C) 2011 Elsevier B.V. All rights reserved.Article Citation - WoS: 22Antibacterial Performance of Pcl-Chitosan Core-Shell Scaffolds(Amer Scientific Publishers, 2018) Ozkan, Ozan; Sasmazel, Hilal TurkogluIn this study, antibacterial performance of the coaxially electrospun Poly-epsilon-caprolactone (PCL)-chitosan core-shell scaffolds developed, optimized and identified physically and chemically in our previous study, were evaluated for the suitability in wound healing applications. The aim of utilizing a core-shell fibrous scaffold with PCL as core and chitosan as shell was to combine natural biocompatibility, biodegradability and antibacterial properties of chitosan with mechanical properties and resistance to enzymatic degradation of PCL. The scaffolds were prepared with the optimized parameters, obtained from our previous study. Thickness and contact angle measurements as well as Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analyses confirmed repeated fabrication of PCL-chitosan core-shell scaffolds. In this study, assays specific to wound dressing materials, such as water vapor transmission rate (WVTR), in vitro degradability and antibacterial tests were carried out. WVTR value of PCL-chitosan core-shell scaffolds was higher (2315 +/- 3.4 g/m(2).day) compared to single PCL scaffolds (1654 +/- 3.2 g/m(2).day) due to the higher inter-fiber pore size. Additionally, in vitro degradability assays showed that the susceptibility of chitosan to enzymatic degradation can be significantly improved by hybridization with more resistant PCL while still keeping the scaffold to be considered as biodegradable. Finally, inhibition ratio and inhibition zone measurements showed that the PCL-chitosan core-shell polymeric scaffolds had significant antibacterial performance (52.860 +/- 2.298% and 49.333 +/- 0.719% inhibition ratios; 13.975 +/- 0.124 mm and 12.117 +/- 0.133 mm clear inhibition zones, against E. coli and S. aureus, respectively), close to the native chitosan. Therefore, the developed scaffolds can be considered as suitable candidates for biodegradable wound dressing applications.Article Citation - WoS: 21Citation - Scopus: 18Dbd Atmospheric Plasma-Modified, Electrospun, Layer-By Polymeric Scaffolds for L929 Fibroblast Cell Cultivation(Taylor & Francis Ltd, 2016) Surucu, Seda; Sasmazel, Hilal TurkogluThis paper reported a study related to atmospheric pressure dielectric barrier discharge (DBD) Ar+O-2 and Ar+N-2 plasma modifications to alter surface properties of 3D PCL/Chitosan/PCL layer-by-layer hybrid scaffolds and to improve mouse fibroblast (L929 ATCC CCL-1) cell attachment, proliferation, and growth. The scaffolds were fabricated using electrospinning technique and each layer was electrospun sequentially on top of the other. The surface modifications were performed with an atmospheric pressure DBD plasma under different gas flow rates (50, 60, 70, 80, 90, and 100sccm) and for different modification times (0.5-7min), and then the chemical and topographical characterizations of the modified samples were done by contact angle (CA) measurements, scanning electron microscopy (SEM), atomic force microscopy, and X-ray photoelectron spectroscopy. The samples modified with Ar+O-2 plasma for 1min under 70cm(3)/min O-2 flow rate (71.077 degrees +/- 3.578) showed a 18.83% decrease compare to unmodified samples' CA value (84.463 degrees +/- 3.864). Comparing with unmodified samples, the average fiber diameter values for plasma-modified samples by Ar+O-2 (1min 70sccm) and Ar+N-2 (40s 70sccm) increased 40.756 and 54.295%, respectively. Additionally, the average inter-fiber pore size values exhibited decrease of 37.699 and 48.463% for the same Ar+O-2 and Ar+N-2 plasma-modified samples, respectively, compare to unmodified samples. Biocompatibility performance was determined with MTT assay, fluorescence, Giemsa, and confocal imaging as well as SEM. The results showed that Ar+O-2-based plasma modification increased the hydrophilicity and oxygen functionality of the surface, thus affecting the cell viability and proliferation on/within scaffolds.Article Citation - WoS: 6Citation - Scopus: 7Hybrid Polymeric Scaffolds Prepared by Micro and Macro Approaches(Taylor & Francis As, 2017) Ozkan, Ozan; Sasmazel, Hilal TurkogluPolymeric scaffolds with complex porous structures were fabricated with two different polymers by combining three fabrication methods in three steps, in which, nonwoven poly(e-caprolactone) microfibers were obtained with electrospinning and immersed in solvent cast chitosan solution poured in Petri dish to fabricate hybrid polymers, and finally the combined structure was freeze-dried with two different predrying techniques to obtain macropores in the structure. The resulting hybrid polymeric mats were found to have both microfibers and macroporosity due to the electrospinning as well as freeze-drying processes, which resemble the natural extracellular matrix. The optimized scaffolds that predried in the incubator at 40 degrees C for 5 h and then freeze-dried for 24 h exhibited contact angle value of 68.93 +/- 2.18 degrees with 3.252 +/- 0.783 MPa Young's modulus and 0.260 +/- 0.002 MPa yield strength as well as 1.35-fold cell yield in MRC5 fibroblast cell culture, compared to the commercial tissue culture polystyrene. [GRAPHICS] .Book Part Poly(ε-caprolactone)/Chitosan Nanostructures for Cell Cultivation(Springer, 2020) Turkoglu Sasmazel,H.Hybridization of synthetic poly (ε-caprolactone) (PCL) and natural chitosan polymers to develop PCL/chitosan core-shell nanostructures for cell cultivation was aimed in this study. Coaxial electrospinning method was used for the fabrication of the nanostructures. The characterizations of the samples were done by X-ray photoelectron spectroscopy (XPS) analyses and mechanical tests. XPS analysis of the PCL/chitosan core-shell structures exhibited the characteristic peaks of PCL and chitosan polymers. The cell culture studies, MTT assay and Confocal Laser Scanning Microscopy (CLSM), carried out with L929 ATCC CCL-1 mouse fibroblast cell line, proved the biocompatibility of all materials. The cell viability on the hybrid nanostructures was ~two times better then on tissue culture polystyrene (TCPS) because of its three dimensional (3D) extracellular matrix (ECM)-like structure compared to 2D flat surface of commercially cell compatible TCPS. The performance was ~two times and ~ten times better compared to single PCL and single chitosan, respectively, even though both fabricated similarly by electrospinning as non-woven fibrous structures, because were either too hydrophobic or too hydrophilic to maintain cell attachment points. © Springer Nature B.V. 2020.
