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Showing 4 results for Scaffold

Sh. Foroutan, M. Hashemian, A. Khandan,
Volume 17, Issue 4 (12-2020)
Abstract

In this article, a novel bio-nanocomposite consists of sodium alginate polymer-based graphene nanosheet enhanced incorporating wollastonite containing various amount of graphene nanosheet were produced using freeze-drying technique. The bio-nanocomposites were mechanically and biologically evaluated using tensile strength and biological test. The phase and topological characterization were conducted using scanning electron microscopy (SEM) and X-ray diffraction (XRD) technique. Subsequently, based upon Euler-Bernoulli and Timoshenko beam theories (EBT and TBT), the buckling responses of the porous bio-nanocomposite soft tissue are analyzed corresponding to various graphene amounts. In order to solve the governing equations a sufficient numerical solution is proposed. Elastic modulus and mass density of the porous bio-nanocomposite are extracted from the experimental tests. The obtained results indicated the sample with 1 wt% graphene sheet has shown proper mechanical and biological features. Therefore, the sample with 1 wt% graphene sheet can be used as potential case for light weight bone substitute applications.

Israa Khahtan Sabree, Batool Abd Aladel Jabar,
Volume 20, Issue 3 (9-2023)
Abstract

Abstract. Hydroxyapatite (HA) scaffold is commonly used in the applications of bone tissue engineering due to its bioactivity and equivalent chemical composition to the inorganic constituents of human bone. The present study focused on the fabrication of porous 3D hydroxyapatite scaffold which was modified by polymer coating as a successful strategy to improve the mechanical properties. A 3D porous hydroxyapatite scaffolds were fabricated by gel-casting method by using freshly extracted egg yolk (EY) with (50 and 60)wt% of HA powder. To enhance the mechanical properties, composite PVA/ HA scaffolds were produced by using dip coating in Polyvinyl alcohol (PVA). Fourier transform infrared spectroscopy (FTIR) was used to recognize the functional group associated with the hydroxyapatite scaffolds before and after PVA coating. The physical (density and porosity) and mechanical (compressive strength and elastic modulus) properties were investigated before and after coating. SEM was used to inspect the surface morphology and pore modification of the scaffolds. Wettability was determined by using a water contact angle to analyze the scaffold hydrophobicity. Surface roughness was studied by atomic force microscopy (AFM). It was revealed that the scaffold porosity decreased with increase solid loading of HA powder in the gel and after PVA coating. The findings showed that PVA coating improved mechanical strength of scaffold to be double by covering the small pores and filling microcracks sited on the scaffold strut surfaces, inducing a crack bridging mechanism. The scaffolds’ strength was in the range of trabecular bone strength. This indicates  non-load bearing applications.

Ahmed Hafedh Mohammed Mohammed, Khairul Anuar Bin Shariff, Mohamad Hafizi Abu Bakar,
Volume 20, Issue 4 (12-2023)
Abstract

The coated β-tricalcium phosphate (β-TCP) with dicalcium phosphate dihydrate (DCPD) has attracted much attention in the biomaterials field due to the increase in its osteoconductivity. Besides, the porous bioceramic scaffolds with controlled pore sizes are significant in stimulating bone-like cell activity. In this study, the effect of the setting-time process and acidic-calcium phosphate (CaP) concentrations on the fabrication and properties of porous DCPD/ β-TCP scaffolds were studied. Subsequently, the specimens were examined using X-ray diffraction (XRD), scanning electron microscopy (SEM), compression strength and Fourier transforms infrared (FTIR). The study results revealed that the porous DCPD/ β-TCP scaffolds with macro- and micropore sizes were successfully obtained after the 300-600 µm of porous β-TCP granules were exposed to an acidic-CaP solution. Furthermore, the setting-time process and acidic-CaP concentrations increased the DCPD interlocking between granules, and the mechanical strengths of scaffolds increased up to 0.5 MPa. Meanwhile, the porosity levels were changed based on the formation of DCPD crystals. This study was expected to provide novel insights to researchers in the field of bioceramics through its investigation on the creation of porous DCPD/ β-TCP scaffolds.

 
Ahad Saeidi, Sara Banijamali, Mojgan Heydari,
Volume 21, Issue 2 (6-2024)
Abstract

This study explores the fabrication, structural analysis, and cytocompatibility of cobalt-doped bioactive glass scaffolds for potential applications in bone tissue engineering. A specific glass composition modified from Hench's original formulation was melted, quenched, and ground to an average particle size of 10 μm. The resulting amorphous powder underwent controlled sintering to form green bodies and was extensively characterized using simultaneous differential thermal analysis (DTA), Raman spectroscopy, and Fourier Transform Infrared analysis (FTIR). After mixing with a resin and a dispersant, the composite was used in digital light processing (DLP) 3D printing to construct scaffolds with interconnected macropores. Thermal post-treatment of 3D printed scaffolds, including debinding (Removing the binder that used for shaping) and sintering, was optimized based on thermogravimetric analysis (TG) and the microstructure was examined using FE-SEM and XRD. In vitro bioactivity was assessed by immersion in simulated body fluid (SBF), while cytocompatibility with MC3T3 cells was evaluated through SEM following a series of ethanol dehydrations. The study validates the fabrication of bioactive glass scaffolds with recognized structural and morphological properties, establishing the effects of cobalt doping on glass behavior and its implications for tissue engineering scaffolds. Results show, Low cobalt levels modify the glass network and reduce its Tg to 529 oC, while higher concentrations enhance the structure in point of its connectivity. XRD results shows all prepared glasses are amorphous nature, and DTA suggests a concentration-dependent Tg relationship. Spectroscopy indicates potential Si-O-Co bonding and effects on SiO2 polymerization. Cobalt's nucleating role promotes crystalline phases, enhancing bioactivity seen in rapid CHA layer formation in SBF, advancing the prospects for bone tissue engineering materials.

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