Prevascularization of tissue equivalents is critical for fulfilling the need for sufficient vascular organization for nutrient and gas transport. Hence, endothelial cell culture on biomaterials is of great importance for researchers. Numerous alternate strategies have been suggested in this sense, with cell-based methods being the most commonly employed. In this study, poly (glycerol sebacate) (PGS) elastomers with varying crosslinking ratios were synthesized and their surfaces were patterned with channels by using laser ablation technique. In order to determine an ideal material for cell culture studies, the elastomers were subsequently mechanically, chemically, and biologically characterized. Following that, human umbilical vein endothelial cells (HUVECs) were seeded into the channels established on the PGS membranes and cultured under various culture conditions to establish the optimal culture parameters. Lastly, the endothelial cell responses to the synthesized PGS elastomers were evaluated. Remarkable cell proliferation and impressive cellular organizations were noticed on the constructs created as part of the investigation. On the concrete output of this research, arrangements in various geometries can be created by laser ablation method and the effects of various molecules, drugs or agents on endothelial cells can be evaluated. The platforms produced can be employed as an intermediate biomaterial layer containing endothelial cells for vascularization of tissue-engineered structures, particularly in layer-by-layer tissue engineering approaches.
Millions of people require bone injury treatment and there have been many methods suggested for the stabilization of bone fractures. The need for the development of new methods is obvious since current stabilization methods are inadequate. Here, we described the development of polyurethane-based bone adhesives composites containing β-tricalcium phosphate ceramics in different sizes and ratios. To characterize the proposed materials, Fourier transform infrared spectroscopy, hydrogen-nuclear magnetic resonance, differential scanning calorimetry analyses together with scanning electron microscopy observations, and micro-computerized tomography imaging were examined. Furthermore, in vitro performance of the produced materials was tested by using MG63 human osteosarcoma cell line, and an ex vivo modeling study was conducted to test the mechanical performance of resulting materials using bovine rib bone. All materials were exhibited high porosity (above 90%) and homogeneous distribution of ceramic particles. Polyurethane scaffolds containing 40% (w/w) 1–2 mm β-tricalcium phosphate were shown the highest compressive strength as 1.34 ± 0.10 MPa. In addition, 85.75% cell viability was recorded according to the cytotoxicity analysis and also the cell proliferation was found highest in the same group. Taken into account the obtained results, the prepared polyurethane-based bone adhesive materials containing ceramics has a great potential to transform into a final product and meet a clinically significant medical need.
Background Decellularized tissues based on well‐conserved extracellular matrices (ECMs) are a common area of research in tissue engineering. Although several decellularization protocols have been suggested for several types of tissues, studies on the optic nerve have been limited. Methods We report decellularization protocol with different detergent for the preparation of acellular optic nerve and tissues were examined. DNA, glycosaminoglycan (GAG), and collagen content of the groups were evaluated with biochemical analyses and examined with histological staining. Mechanical properties, chemical components as well as cytotoxic properties of tissues were compared. Results According to the results, it was determined that TX‐100 (Triton X‐100) was insufficient in decellularization when used alone. In addition, it was noticed that 85% of GAG content was preserved by using TX‐100 and TX‐100‐SD (sodium deoxycholate), while this ratio was calculated as 30% for SDS. In contrast, the effect of the decellularization protocols on ECM structure of the tissues was evaluated by scanning and transmission electron microscopy (SEM and TEM) and determined their mechanical properties. Cytotoxicity analyses were exhibited minimum 95% cell viability for all groups, suggesting that there are no cytotoxic properties of the methods on L929 mouse fibroblast cells. Conclusions The combination of TX‐100‐SD and TX‐100‐SDS (sodium dodecyl sulfate) were was determined as the most effective methods to the literature for optic nerve decellularization.
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