Papers by Keyword: Scaffold

Abstract: Using the sol-gel process, glass powder was made. After the preparation method of the glass powder, x-ray analytical (XRD), particle size analysis and Fourier Transform Infrared (FTIR) were performed. The particle size analysis of manufactured glass (13-93) is found to be about 2.978 μm. (XRD) mode analysis suggested that the resulting porous scaffolds were amorphous. Using the process of salt leaching to create bioactive glass scaffolds (13-93) with structural and physical properties suitable for the human trabecular bone. XRD spectroscopy, scanning electron microscopy (SEM) and FTIR after sintering at temperature 750 °C were used to investigate the microstructure and chemical bonding of the porous scaffolds. The synthesized scaffold was soaked in medium of the simulated body fluid (SBF) and examined by SEM and XRD analysis in order to evaluate bioactivity. From the SEM morphology analysis results, it was noticed that the scaffolds comprised open and interconnected pores with a porosity range of 75-78%. High bioactivity of pours scaffolds was reported to have been observed after soaking 7days in SBF media because of the formation of apatite layer on its surfaces. Keywords: bioactive glass (13-93), scaffold, salt leaching method, SBF, sol-gel.

Abstract: Utilization of natural biopolymers has shown potential in generating innovations for tissue engineering applications. This study aims to fabricate scaffolds from cellulose acetate derived from kapok fiber. Cellulose is extracted from raw kapok fibers by alkali treatment and delignification then synthesized into cellulose acetate. Kapok cellulose acetate (KCA) is dissolved in dimethyl sulfoxide to fabricate the scaffold. Materials were characterized using Attenuated Total Reflectance – Fourier Transform Infrared (ATR-FTIR) spectrometer, X-ray diffractometer (XRD) and Differential Scanning Calorimeter (DSC). FTIR analysis has shown that cellulose was extracted from kapok and cellulose acetate was successfully synthesized. XRD analysis also confirmed the presence of cellulose acetate. Results have also shown that synthesized KCA seems to have higher crystallinity than commercially available cellulose acetate (CCA). The degree of substitution (DS) of KCA was found to be 2.85 which is close to the DS value of tri-substituted cellulose acetate. DSC analysis has shown lower glass transition temperature of 52.15°C but higher degradation temperature of 300.43°C than the CCA. Moreover, the values for the enthalpy of fusion for two endotherms of KCA (44.0556 J/g and 18.6946 J/g) are higher than the values for CCA by 344% and 261%, respectively; thus, indicating the higher degree of crystallinity for synthesized KCA samples.

Abstract: The demand for wound management treatment especially advanced and active wound care products is huge. In this study, the scaffolds were prepared from gellan gum (GG) incorporated ball clay (BC) at different concentrations to investigate their swelling properties, water vapor transmission rates (WVTR), mechanical characteristic and thermal behavior. There are three different concentrations of BC were added into the GG scaffolds which were 5% w/w (GG/BC5), 10% w/w (GG/BC10) and 15% w/w (GG/BC15). Swelling ratio of GG scaffolds were increased upon addition of ball clay, while WVTR values of all scaffolds were decreased in the range of 1081–1164 g m⁻² d⁻¹. The mechanical performance results show that the GG/BC10 has the highest compressive stress at break (26 ± 5 MPa) and compressive strain at break (110 ± 21%). For thermal behavior, it shows that the thermal stability of GG scaffolds had improved after the addition of ball clay attributed to the interaction between GG and ball clay. The results show that the GG/BC scaffolds could be a potential candidate to be used as an active wound care product.

Abstract: Electrospinning technique is widely investigated in medical applications such as tissue engineering scaffolds, wound dressing and drug delivery. In this study, the aligned nanofiber scaffold of Eudragit RS100 was successfully fabricated via electrospinning technique for nerve tissue engineering scaffold. The diameter distribution and degree of alignment of Eudragit RS100 nanofiber scaffold were observed by scanning electron microspore (SEM). The chemical and crystalline structure of Eudragit RS100 nanofiber scaffold were analyzed using Fourier transform infrared spectroscopy (FTIR) and Powder X-ray diffactometer (PXRD). Cell culture studies using rat Schwann cells were determined to evaluate cell proliferation cell alignment and morphology. The results implied that the diameter of fiber was in the nanometer region. The Eudragit RS100 nanofiber scaffold were in an amorphous form and its chemical structure was not destructive after the electrospinning process. The Eudragit RS100 nanofiber scaffold showed biocompatibility with rat Schwann cells and growing parallel to the aligned fibers. In conclusion, the Eudragit RS100 nanofiber scaffold may have the ability to apply to nerve tissue engineering scaffold.

Abstract: The bone scaffold is susceptible to infection in its application due to the bacteria that often appear on the surface. To prevent this phenomenon, the scaffolds need to be modified in order to provide antibacterial properties. In this study, the bone scaffold was fabricated from chitosan-collagen with the addition of zinc oxide as an antibacterial agent. There were four variables of the amount of zinc oxide added to the scaffold: 0%, 1%, 3%, and 5%. The method used was Thermally Induced Phase Separation (TIPS). From this study, a porous scaffold with a rough surface was obtained. SEM image of the scaffold showed that more zinc oxide caused smaller pore and lower porosity. Characterization with FTIR proved that the scaffold obtained from this process has the same functional group as chitosan and collagen. The DSC-TGA curve confirmed that the heating process performed on dehydrothermal treatment (DHT) did not cause degradation of the scaffold because chitosan and collagen have higher degradation temperatures than DHT temperatures. In addition, this study also proved that the addition of zinc oxide had successfully provided the scaffold with antibacterial properties in which the protection against bacteria was related to the amount of zinc oxide in direct proportion.

Abstract: Smart thermosensitive polymer such as poly (N-isopropyl acrylamide) (PNIPAM) and dominant fibrous protein of connective tissue such as collagen (CLG) possess great potential in biomedical and tissue engineering applications. The objectives of current work aim to explore potential of PNIPAM and collagen by (i) establish a stable procedure to extract collagen from fresh water Tilapia fish scale (TFS) and (ii) fabricate PNIPAM and hybrid PNIPAM-CLG nanofibrous scaffolds through electrospinning technique and investigate their material-process-structure behaviour. Type I collagen was derived through acid hydrolysis of TFS. Electrospinning of PNIPAM was carried out with 16, 18 and 20 wt% PNIPAM concentration in methanol (MeOH) while PNIPAM-CLG was prepared through blending measured quantity of PNIPAM dissolved in water with collagen dissolved in acetic acid. Material properties, viscosity, morphology and thermo-physical behaviors of the derived collagen, electrospun PNIPAM and PNIPAM-CLG scaffolds were characterized. Results from SDS-PAGE and FTIR confirmed that the isolated TFS collagen is of type I. EDX revealed that demineralization eliminated the aluminium, magnesium, silicon and phosphorus while significantly reduced the sulfur elements from raw TFS. SEM observation of the collagen morphology shown a fluffy and fibrillary lamellae structure. Electrospun scaffolds were successfully fabricated with 16 and 18 wt% PNIPAM in MeOH. Both homogeneity and average fibre diameter (D_avg) were greater in the 18 wt% PNIPAM scaffold, in which the D_avg for 16 and 18 wt% were ~110 and ~131.7 nm respectively. However, PNIPAM at 20 wt% failed to be electrospun owing to its excessively high viscosity. On the other hand, SEM observation revealed that the electrospun hybrid PNIPAM-CLG scaffold has D_avg of ~105.5 nm amid the presence of numerous elongated beads.

Abstract: Bovine bone is a considerable source for the production of hydroxyapatite. The recent study reported a novel method to extract hydroxyapatite from bovine bone without producing hazardous residue. The bovine bones were cut and boiled in the opened chamber followed by boiling in pressurized tank. The bones were then soaked into 95% ethanol. Calcination was then conducted in 800°C, 900°C and 1,000°C, for 2 hours. The result was then grinded and sieved. The powder then was characterized using Fourier transform infrared (FT-IR), Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) to measure the purity of hydroxyapatite. It is concluded that the hydroxyapatite derived from this process showed 100% purity, resulting 35.34 ± 0.39% w/w from the wet bone weight and 72.3% w/w from the dried weight. The present extraction method has been proven to yield high amount of pure hydroxyapatite as well as reducing the use of hazardous reagent.

Abstract: The finite element simulation of compression test of a lattice structure, made of Ti-6-4, produced by additive technology, was implemented. The cellular material was designed from the intersecting cylindrical struts with the orthogonal arrangement of horizontal and vertical struts. The distribution of equivalent stresses was estimated. The most loaded were the struts, the axis of which was parallel to the axis of loading. The maximum equivalent stresses were observed at the junction of struts. The analysis of the cross-section of the struts revealed that equivalent stresses in the central regions of the struts were about 50% less than those on the surface.

Abstract: Replacement of in vivo testing using advanced 3D constructs is an important challenge in tissue engineering applications. The cell culture material should be biocompatible and should mimic the natural microenvironment of the existing tissue. Nanofibrous scaffolds prepared by electrospinning from biocompatible polymers have suitable properties for cell culture in a 3D environment. Thanks to the high volume-to-surface ratio, controlled porous structure with high pore interconnection and microarchitecture in the nanoscale range, nanofibers are in the foreground of interest. We tested membranes with different topography with keratinocyte and fibroblast cell lines. Fibroblast showed stable growth with no difference among the scaffolds. On the other hand, keratinocytes preferred scaffolds with nanofiber morphology.

Abstract: The ceramics in the system CaO–MgO–SiO₂ has recently attracted a great deal of attention because they display a good in vitro bioactivity and have potential use as bone implants. Biphasic calcium-magnesium-silicate ceramics were prepared by a sol-gel method. The dried gel with chemical composition 3CaO.MgO.2SiO₂ was thermally treated at 1200 °C for 2 hrs. The structural behavior of the synthesized ceramics was examined by means of X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). Merwinite crystalline phase and akermanite phase were recognized. Then, porous akermanite/merwinite scaffolds were prepared to utilize polymer sponge method and evaluated by employing SEM. Furthermore, bone marrow stromal cells (BMSC) adhesion and proliferation on the scaffolds were evaluated by MTT assay test. Differentiation of the cells was assessed by measuring alkaline phosphatase (ALP) activity. The results demonstrated that BMSC adhered and spread well on akermanite scaffolds and proliferated with the increase in the culture time, and the differentiation rate of osteoblasts on scaffolds was comparable to that on blank culture plate control. Thus, the obtained results presented that the akermanite/merwinite scaffolds deserve attention for bone tissue engineering applications.