Papers by Keyword: Scaffold

Abstract: This study investigates the morphological, structural, and bioactive properties of strontium-doped bioactive glass (Sr-BG) and copper-strontium-doped bioactive glass (Cu-Sr-BG) scaffolds to enhance their potential for biomedical applications. Scanning electron microscopy (SEM) revealed that both Sr-BG and Cu-Sr-BG scaffolds feature smooth, highly porous surface morphologies with interconnected pores (120–150 µm) created using a foaming agent. This pore network facilitates cell attachment and proliferation. Fourier transform infrared (FTIR) analysis confirmed the preservation of the silica network, with characteristic Si–O–Si bending and stretching peaks remaining consistent after Cu doping. X-ray diffraction (XRD) analysis demonstrated that both scaffolds retained an amorphous structure, with Cu doping successfully incorporated without disrupting this feature. Both Sr-BG and Cu-Sr-BG scaffolds exhibited excellent bioactivity, forming an apatite layer on their surfaces after immersion in simulated body fluid (SBF), indicating strong potential for bone tissue engineering applications. These findings suggest that Sr-and Cu-doped bioactive glass scaffolds possess promising characteristics for promoting cell attachment and osteoconductivity, positioning them as viable candidates for future biomedical applications in bone regeneration

Abstract: Nowadays, the requirements of scaffolds and bone grafts are increasing along with large defects increasing every year. Furthermore, large defects that occur in human bones are customary. However, this obstacle can be overcome by using 3D printing. This study aims to investigate the morphology, deviation dimension, shrinkage and hardness of hydroxyapatite (HA)/collagen composite, which these materials mimic with human bone. HA/collagen composite was printed using three-dimensional bioprinting based on extrusion with a print speed of 10 mm/min and a layer height of 0.5 mm. The composition of HA and collagen material is 70% and 30%, respectively, where this composition mimics natural bone. Morphology and dimension of HA/collagen composite were obtained by transmission electron microscope. Moreover, the deviation dimension and shrinkage were measured using the Miviewcap optical microscope and software Image J. The resulting HA/collagen composite clearly showed that collagen was in the form of fibers while HA was in an irregular shape. The average width and length of collagen were 5.98 + 0.20 nm and 82.48 + 6.23 nm, respectively. Moreover, the Average width and length of HA were 21.85 + 0.53 nm and 23.30 + 1.33 nm. The average deviation dimension in the X, Y, and Z axes was 2.69%, 1.40%, and 24.12%. Furthermore, shrinkage was 12.27%, 10.18%, and 19.06% on the X, Y, and Z axes. The average hardness of specimen 1 and 2 of HA/collagen composite were 0.0021594 HV.

Abstract: Scaffold Carbonated Hydroxyapatite/Honeycomb/Polyethylene Oxide (CHA/HCB/PEO) has been obtained by freeze-drying. The bioceramic CHA used in this study was synthesized from oyster shells using precipitation. HCB and PEO were added as reinforcement materials that affect the crystallographic properties of the scaffold. This study aimed to determine the characteristics of the scaffolds for bone tissue engineering. CHA and scaffolds were characterized using Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffractometer (XRD), and Scanning Electron Microscopy (SEM). FTIR spectra and XRD graphs confirmed that the CHA produced was B-type. FTIR spectra of the scaffold showed the presence of HCB and PEO in the scaffold, which means they were homogeneously bound in the scaffold solution. XRD test results show that scaffolds' crystallinity and crystallite size tends to decrease compared to CHA. This was good because they could make cells easier to proliferate. A small-scale pore structure (micropore) was also formed in the scaffold. The porosity and pore size of the scaffold were affected by the concentration of CHA. The presence of the micropores can increase the permeability of the scaffold and facilitate cell migration. Thus, the composition of CHA/HCB/PEO scaffolds can be a good candidate material in bone tissue engineering.

Abstract: Microwave heating was used with a gas foaming method for fabricating limestone carbonated hydroxyapatite scaffold (SCHA). Carbonated hydroxyapatite (CHA) was produced from limestone as a calcium source using the co-precipitation method. For further treatment, 0.6 gr CHA powder was mixed in 1 ml H₂O₂ solution as a blowing agent. The slurry-foam-like CHA was heated in a microwave with different levels of heating power from 180 W to 720 W. The SCHA samples were characterized using X-ray diffraction (XRD), Fourier-transform infrared (FTIR), and Scanning electron microscope (SEM). The crystallinity and crystallite size were affected due to different rates of heating power in the microwave-assisted method. The increasing temperature decreased the crystallite size from 37.49 to 33.97(nm). However, other crystallinity trends were observed at 180 W because the lower power heating needed a longer time to be formed SCHA. The different power rates have an insignificant contribution to the morphology of the scaffolds.

Abstract: Bone tissue engineering has been used in the biomedical field to treat bone defects by implanting scaffolds into bone tissue. However, the currently developed scaffold still needs to be developed to obtain scaffold building materials with good compatible properties and can regenerate damaged bone cells. This study combines PVA/Chitosan polymer with CHA of tuna bone using the porogen leaching method at a calcination temperature of 100°C for 12 hours. The purpose of this study was to determine the physicochemical properties by characterizing XRD, SEM-EDX, FTIR, and the porosity of the scaffold. The results obtained from the results of the PVA/Chitosan/CHA XRD patterns are the formation of the PVA/Chitosan phase at 2θ(°)=19.68, the IR spectrum of the 𝑃𝑂₄³⁻group band and 𝐶𝐻₂ stretching, the ratio mol Ca/P is 1.98, the pore diameter is 1.561 ± 0.07 μm and the porosity is 55.04%. These results indicate that the PVA/Chitosan/CHA scaffold is an amorphous calcium phosphate (ACP) that has the potential for bone tissue engineering.

Abstract: Electrospinning is a cost-effective and versatile technique to fabricate continuous fibers ranging from submicron diameter to nanometer diameter. Polybutylene adipate-co-terephthalate (PBAT) has been investigated as a fibrous scaffold because of its low crystallinity, rapid biodegradability, and excellent mechanical properties, particularly for its high toughness and flexibility. However, the potential of the PBAT fibrous scaffold for medical purposes is still limited. PBAT blends with biocompatible polymers have been developed and investigated for tissue engineering applications. Herein, the preliminary research examines the processability of neat PBAT as a fibrous scaffold by varying several electrospinning processing parameters, such as solution concentration, voltage, flow rate, and tip to collector distance. The aim is to obtain continuous, smooth, and bead-free fibers. The electrospun fibers were examined using a scanning electron microscope (SEM) to determine its diameters. The optimum parameters for obtaining a continuous, bead-free PBAT fibrous scaffold were 20% w/v concentration, 19 kV voltage, 2 mL/h flow rate, and a 15 cm distance.

Abstract: In this study, a synthetic scaffold was prepared from polycaprolactone (PCL) and polyurethane (PU) blend, in a ratio of [2:1] [PCL: PU], using electrospinning technique. Electrospun scaffolds from native PCL and PU were also prepared for comparison, using the same polymer concentration 15% weight/ volume w/v. The detailed microstructure and other properties, like mechanical properties, porosity, and contact angle were investigated and compared between the three prepared scaffolds. Then, the survival, adhesion, proliferation and penetration of rat embryonic fibroblast (REF) cells were evaluated on these three prepared scaffolds after being in vitro cultured with these cells for 21 days, using scanning electron microscope (SEM) analysis and histological analysis. The results showed that, all the studied properties, including mechanical properties and contact angle were enhanced by combining PU with PCL in the [PCL: PU] scaffold. The average diameter of fiber and the average size of pore were suitable and proper for cell attachment, cell proliferation, and also the big average pore size in [PCL: PU] scaffold was enough for cell penetration to form a three- dimension 3-D structure, which is the aim of this study.

Abstract: Poly (N-isopropylacrylamide) (PNIPAm) has been one of the most widely studied thermal responsive polymer in tissue engineering owing to its reversible hydrophilic-hydrophobic phase transition across its lower critical solution temperature (~32°C) that is close to human physiological temperatures. Among tissue engineering constructs, nanofibrous scaffolds offer an added advantage in mimicking the morphology of the native extracellular matrix (ECM). Electrospinning has been reported as one of the most facile method to produce PNIPAm nanofibres and neat electrospun nanofibres scaffold is known to possess poor aqueous stability, limiting its use in tissue engineering applications. In contrast, numerous studies on PNIPAm hydrogels have shown relatively good aqueous stability owing to the hydrophilic 3D crosslinked structure of the hydrogel which resist instant dissolution but rather swell to a greater or lesser extent. However, the presence of crosslinkages in PNIPAm hydrogels causes it to be hardly electrospinnable into nanofibres. In the present work, crosslinker free PNIPAm was radical polymerized to a high molecular weight of 385 kDa. To produce nanofibers, electrospinning was carried out on a dedicated %wt of PNIPAm solution containing octaglycidyl polyhedral oligomeric silsesquioxane (OpePOSS) and 2-ethyl-4-methylimidazole (EMI). Resulting PNIPAm nanofibrous network was found to strongly resemble the ECM morphology with fiber diameter of 436.35 ± 187.04 nm, pore size 1.24 ± 1.27 μm and 63.6% total porosity. Aqueous stability was studied in cell culture media over the course of 28 days. The current result shows significant improvement with a gradual mass loss up to a maximum of 35% instead of the near immediate dissolution observed in the case of electrospun neat PNIPAm scaffold without crosslinks.

Abstract: The use of mesenchymal stem cells can add local improvements potential to enthesis tissue regeneration based on tropical activity through secretions of growth factors, cytokines, and vesicles (e.g. exosomes), collectively known as secretomes. This study aims to analyze secretomes characterization from adipose-derived mesenchymal stem cells seeded with enthesis tissue scaffold in hypoxic conditions and to analyze the influence of hypoxic environment to the characterization of secretomes. This is an in-vitro study using a Randomized Control Group Post-Test Only design. This study using Adipose Stem Cells (ASCs) were cultured in hypoxia (Oxygen 5%) and Normoxia (21%) condition. The scaffolds are fresh-frozen enthesis tissue and was seeded in the treatment group and compared to control. The evaluation of Scleraxis (Scx) and SRY-box (Sox9) was measured using ELISA on the 2nd, 4th, and 6th days. Comparison of Scx levels between each evaluation time showed a positive trend in a group with scaffold in hypoxia condition although it has no significant differences (p=0.085), with the highest level on day 6, that is 13,568 ng/ml. Conversely, the comparison of Sox9 showed significant differences (p=0.02) in a group with scaffold in hypoxia condition, with the highest level on day 4, that is 28,250 ng/ml. The use of enthesis scaffold seeded in adipose-derived mesenchymal stem cells in hypoxic conditions shows a positive trend as regenerative effort of injured enthesis tissue through Scleraxis and Sox9 secretomes induction.

Abstract: The tissue engineering approach for periodontal tissue regeneration using a combination of stem cells and scaffold has been vastly developed. Mesenchymal Stem Cells (MSCs) seeded with Bovine Teeth Scaffold (BTSc) can repair alveolar bone damage in periodontitis cases. The alveolar bone regeneration process was analyzed by micro-computed tomography (µ-CT) to observe the structure of bone growth and to visualize the scaffold in 3-Dimensional (3D). The purpose of this study is to analyze alveolar bone regeneration by µ-CT following the combination of MSCs and bovine teeth scaffold (MSCs-BTSc) implantation in the Wistar rat periodontitis model. Methods. MSCs were cultured from adipose-derived mesenchymal stem cells of rats. BTSc was taken from bovine teeth and freeze-dried with a particle size of 150-355 µm. MSCs were seeded on BTSc for 24 hours and transplanted in a rat model of periodontitis. Thirty-five Wistar rats were made as periodontitis models with LPS induction from P. gingivalis injected to the buccal section of interproximal gingiva between the first and the second mandibular right-molar teeth for six weeks. There were seven groups (control group, BTSc group on day 7, BTSc group on day 14, BTSc group on day 28, MSCs-BTSc group on day 7, MSCs-BTSc group on day 14, MSCs-BTSc group on day 28). The mandibular alveolar bone was analyzed and visualized in 3D with µ-CT to observe any new bone growth. Statistical Analysis. Group data were subjected to the Kruskal Wallis test followed by the Mann-Whitney (p <0.05). The µ-CT qualitative analysis shows a fibrous structure, which indicates the existence of new bone regeneration. Quantitative analysis of the periodontitis model showed a significant difference between the control model and the model with the alveolar bone resorption (p <0.05). The bone volume and density measurements revealed that the MSCs-BTSc group on day 28 formed new bone compared to other groups (p <0.05). Administration of MSCs-BTSc combination has the potential to form new alveolar bone.