Nanobioactive Glass Research Articles

Facile fabrication of nano-bioactive glass functionalized blended hydrogel with nucleus pulposus-derived MSCs to improve regeneration potential in treatment of disc degeneration by in vivo rat model

Orthopaedic medicine often treats intervertebral disc degeneration (IVDD), which is caused by nucleus pulposus (NP) tissue damage and mechanical stress. Bioactive glasses (BGs), widely used for bone regeneration, can incorporate therapeutic ions into their network. Manganese (Mn) activates human osteoblast integrins, proliferation, and spreading. The CMnBGNPs-NPMSCs are carboxymethyl cellulose hydrogels functionalized with MnBGsNPs and NP-derived mesenchymal stem cells to treat IVDD. To ensure stability and biocompatibility of CMnBGNPs-NPMSCs were characterized for rheological properties like gelation time and swelling ratio. Gene expression analysis of PAX1, FOXF1, CA12, HBB, and OVOS2 via qRT-PCR further assessed the hydrogel's characteristics. Rat models with induced IVDD had hydrogel-MSC composite injected into their intervertebral discs for in vivo studies. Histological examination, immunohistochemical staining for inflammation and disc regeneration markers, and disc height assessments assessed therapeutic efficacy. CMnBGNPs-NPMSCs show promising results for IVDD treatment, offering a novel therapeutic strategy with clinical implications for degenerative disc diseases.

Aqueous electrophoretic deposition of yttrium-doped nanobioactive glass/collagen/chitosan orthopedic coatings on 316L SS

The current study used yttrium-doped nanobioactive glass (Y-nBG), based on 62 SiO2 – (33 – x) CaO – 5 P2O5 – x Y2O3 mole % system (x = 0 and 3 mol %), collagen, and chitosan composites for coating 316L stainless steel (316L SS) using aqueous electrophoretic deposition (EPD) technique. The corresponding coated samples are encoded as SS/Col-Chit, SS/BG-Y0/Col-Chit, and SS/BG-Y3/Col-Chit, respectively. Physicochemical characterization implied TGA, FTIR, SEM-EDX, contact angle, adhesion strength and in vitro bioactivity in SBF were performed. Following SBF immersion, FTIR and SEM-EDX investigations were also carried out. Furthermore, the coatings were loaded with gentamicin drug; the drug-release profile and mechanism were evaluated. The antibacterial efficacy of the composite coatings was also assessed. The results showed the formation of homogeneous coatings with good adhesion strength, 1.39 MPa, 0.55 MPa, and 0.81 MPa, and enhanced the wettability by decreasing the contact angle 36⁰, 22⁰ and 12⁰ for SS/Col-Chit, SS/BG-Y0/Col-Chit and SS/BG-Y3/Col-Chit coatings, respectively. In vitro bioactivity of coatings containing nBG revealed apatite formation after immersion in SBF. Furthermore, the antibiotic gentamicin showed a sustained release profile over time by diffusion mechanisms based on the Higuchi, Fickian, and Weibull models. As well, all coatings containing drugs have an antibacterial effect. Overall, these findings suggested that the prepared coatings have potential applications as orthopedic and dental implants.

Evaluation of Mechanical and Elemental Properties of Bioceramic-Coated Orthodontic Brackets and Enamel Surface.

The aim is to coat orthodontic brackets with two different bioactive materials and to compare the mechanical and morphological properties of coated brackets and tooth surfaces. A total of 120 stainless steel brackets were divided equally into three groups, that is, the uncoated brackets and nanohydroxyapatite (nHA)-coated, and nanobioactive glass (nBG)-coated brackets using a spin coater machine. The brackets were bonded on the enamel surface and underwent remineralization/demineralization cycles for days 1, 7, 14, and 30. At each time interval, the bond strength of the brackets was assessed using mechanical loading. An optical and scanning electron microscope (SEM) were used for surface evaluation, and the adhesive remanent index (ARI) values were obtained and quantified. One-way analysis of variance using Tukey's test was used to compare the differences among the groups. A uniform distribution of nanoparticles occurred on the surfaces of brackets. The shear bond strength (SBS) showed no significant differences in any tested groups on days 1, 7, and 14. However, control and nBG showed a significant difference from nHA at day 30. On days 7, 14, and 30, the nHA group showed the highest SBS values among the groups. For ARI, most samples showed an adhesive nature of failure at the enamel-brackets interface. The images confirmed the presence of coated particles on brackets and remnants of adhesives after SBS. This study confirmed that the nHA- and nBG-coated brackets have a high potential for application in orthodontics regarding structural and mechanical properties.

A novel injectable boron doped-mesoporous nano bioactive glass loaded-alginate composite hydrogel as a pulpotomy filling biomaterial for dentin regeneration

BackgroundDifferent materials have been used as wound dressings after vital pulp therapies. Some of them have limitations such as delayed setting, difficult administration, slight degree of cytotoxicity, crown discoloration and high cost. Therefore, to overcome these disadvantages, composite scaffolds have been used in regenerative dentistry. This study aims to construct and characterize the physicochemical behavior of a novel injectable alginate hydrogel loaded with different bioactive glass nanoparticles in various concentrations as a regenerative pulpotomy filling material.MethodsAlginate hydrogels were prepared by dissolving alginate powder in alcoholic distilled water containing mesoporous bioactive glass nanoparticles (MBG NPs) or boron-doped MBG NPs (BMBG NPs) at 10 and 20 wt% concentrations. The mixture was stirred and incubated overnight in a water bath at 50 0 C to ensure complete solubility. A sterile dual-syringe system was used to mix the alginate solution with 20 wt% calcium chloride solution, forming the hydrogel upon extrusion. Then, constructed hydrogel specimens from all groups were characterized by FTIR, SEM, water uptake percentage (WA%), bioactivity and ion release, and cytotoxicity. Statistical analysis was done using One-Way ANOVA test for comparisons between groups, followed by multiple pairwise comparisons using Bonferroni adjusted significance level (p < 0.05).ResultsAlginate/BMBG loaded groups exhibited remarkable increase in porosity and pore size diameter [IIB1 (168), IIB2 (183) (µm)]. Similarly, WA% increased (~ 800%) which was statistically significant (p < 0.05). Alginate/BMBG loaded groups exhibited the strongest bioactive capability displaying prominent clusters of hydroxyapatite precipitates on hydrogel surfaces. Ca/P ratio of precipitates in IIA2 and IIB1 (1.6) were like Ca/P ratio for stoichiometric pure hydroxyapatite (1.67). MTT assay data revealed that the cell viability % of human gingival fibroblast cells have declined with increasing the concentration of both powders and hydrogel extracts in all groups after 24 and 48 h but still higher than the accepted cell viability % of (˃70%).ConclusionsThe outstanding laboratory performance of the injectable alginate/BMBGNPs (20 wt%) composite hydrogel suggested it as promising candidate for pulpotomy filling material potentially enhancing dentin regeneration in clinical applications.

Productizing Nano-Bioactive Glass-Based Bilayer Scaffolds: A Graft for Reconstruction of Mandibular and Femoral Bone Defects.

This investigation aimed to construct a bilayer scaffold integrating alginate and gelatin with nanobioactive glass (BG), recognized for their efficacy in tissue regeneration and drug delivery. Scaffolds, namely, alginate/gelatin (AG), alginate-/actonel gelatin (AGD), alginate actenol/gelatin-45S5 BG (4AGD), and alginate-actonel/gelatin-59S BG (5AGD), were assembled using a cost-effective freeze-drying method, followed by detailed structural investigation via powder X-ray diffraction as well as morphological characterization using field emission scanning electron microscopy (FESEM). FESEM revealed a honeycomb-like morphology with distinct pore sizes for nutrient, oxygen, and drug transport. The scaffolds evidently exhibited hemocompatibility, high porosity, good swelling capacity, and biodegradability. In vitro studies demonstrated sustained drug release, particularly for scaffolds containing actonel. In vivo tests showed that the bilayer scaffold promoted new bone formation, surpassing the control group in bone area increase. The interaction of the scaffold with collagen and released ions improved the osteoblastic function and bone volume fraction. The findings suggest that this bilayer scaffold could be beneficial for treating critical-sized bone defects, especially in the mandibular and femoral regions.

Osteogenic Differentiation and Proliferation of Apical Papilla Stem Cells Using Chitosan-Coated Nanohydroxyapatite and Bioactive Glass Nanoparticles.

The aim of this study was to evaluate the osteogenic differentiation ability and proliferation of apical papilla stem cells (SCAPs) using chitosan-coated nanohydroxyapatite and bioactive glass nanoparticles. Hydroxyapatite, chitosan-coated nanohydroxyapatite, and bioactive glass 45S5 nanoparticles were prepared and characterized using a transmission electron microscope and X-ray diffraction. SCAPs were harvested from freshly extracted impacted wisdom teeth, cultured, and characterized using flow cytometric analysis. Tested nanomaterials were mixed and samples were classified into five equal groups as follows: negative control group: SCAP with Dulbecco's modified eagle's medium, positive control group: SCAP with inductive media, first experimental group: nanohydroxyapatite with SCAP, second experimental group: chitosan-coated nanohydroxyapatite with SCAP, third experimental group: bioactive glass nanoparticles with SCAP. Osteoblastic differentiation was assessed using an alkaline phosphatase (ALP) assay. Receptor activator of nuclear factor kappa beta ligand (RANKL) expression was evaluated using specific polyclonal antibodies by fluorescence microscope. The proliferation of SCAP was assessed using cell count and viability of trypan blue in addition to an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Isolated SCAP showed a nonhematopoietic origin. Chitosan-coated nanohydroxyapatite showed the highest ALP concentration followed by nanobioactive glass, nanohydroxyapatite, and negative control. Chitosan-coated nanohydroxyapatite showed the highest H score followed by nanobioactive glass, nanohydroxyapatite, and negative control in RANKL expression. Chitosan-coated nanohydroxyapatite showed the highest viable cell count. SCAP isolation is achievable from extracted fully impacted immature third molars. All tested biomaterials have the ability to induce osteogenic differentiation and proliferation of SCAP. Composite nanoparticle materials show better osteogenic differentiation and proliferation of SCAP than single nanoparticles.

Microshear Bond Strength of Nano-filled Resin Composite to Remineralized Tooth Tissues Using Nano-Bioactive Glass

Microshear Bond Strength of Nano-filled Resin Composite to Remineralized Tooth Tissues Using Nano-Bioactive Glass

The Effect of Different Percentages of Nano-bioactive Glass in the Synthesized CPP/ACP Paste on the Remineralization of Demineralized Enamel

Background: The preventive treatments of primary caries lesions are essential for preventing destructive damage to the tooth structure. One of the common treatments is the application of casein phosphopeptide-amorphous calcium phosphate (CCP/ACP) paste on the enamel surface. The aim of this study was to investigate the effect of different percentages of nano-bioactive glass (nBG) incorporation into synthesized CPP/ACP paste on the remineralization of demineralized enamel. Methods: In general, 24 extracted human intact premolar teeth were selected, and their crowns were removed for this purpose. Each crown was cut into two halves, and each half was considered as a sample. The samples were placed in a demineralizing solution at a pH rate of 4.6 for 8 hours, in artificial saliva for 1 hour, and again in a remineralizing solution at a pH rate of 7 for 15 hours. The pH cycling was performed for 14 days to demineralize the enamel surface. The samples were randomly divided into 3 groups (n=16), including G1 (without treatment), G2 (treated with synthesized CPP/ ACP paste containing 5% nanobioglass), and G3 (treated with synthesized CPP/ACP paste containing 10% nanobioglass). The paste was then placed directly on the surface of the demineralized enamel for 4 minutes (twice a day for 28 days). The samples were subjected to the Vickers microhardness test. Finally, data were analyzed using SPSS (version 19) and the analysis of variance and Tukey’s tests (α = 0.05). Results: There was a significant difference between microhardness values in G1 and G2, as well as G1 and G3 (P&lt;0.05). However, no statistically significant difference was observed between G2 and G3 (P&gt;0.05). Conclusions: The results showed adding bioactive glass into synthetic CPP/ACP paste increases enamel remineralization in spite of the percentage of bioactive glass incorporation.

Fabrication and characterization of chlorhexidine gluconate loaded poly(vinyl alcohol)/45S5 nano-bioactive glass nanofibrous membrane for guided tissue regeneration applications.

Polymeric barrier membranes are used in periodontal applications to prevent fibroblastic cell migration into the cavities of bone tissue and to properly guide the proliferation of tissues. In this study, the fabrication, characterization, bioactivity, and in vitro biological properties of polyvinyl alcohol-based nanofibrous membranes containing nano-sized 45S5 bioactive glass (BG) loaded with chlorhexidine (CH) gluconate with biocompatible, bioactive, and antibacterial properties for using as dental barrier membranes were investigated. Nanofibrous membranes with an average fiber diameter, pore size, and porosity of 210 nm, 24.73 μm, and 12.42%, respectively, were loaded with 1% and 2% CH, and the release profile was investigated. The presence of BG in the membranes promoted fibroblastic proliferation and the presence of CH provided antibacterial properties. Nanofibrous membranes exhibit a high ability to restrict bacterial growth while fulfilling the necessary conditions for use as a dental barrier thanks to their low swelling rates, significant surface bioactivities, and appropriate degradation levels.

Effect of hydrogen peroxide and its combination with nano-hydroxyapatite or nano-bioactive glass on the enamel demineralization and tooth color: An in vitro study

Effect of hydrogen peroxide and its combination with nano-hydroxyapatite or nano-bioactive glass on the enamel demineralization and tooth color: An in vitro study

Synthesis and characterization of nano bioactive glass for improving enamel remineralization ability of casein phosphopeptide–amorphous calcium phosphate (CPP-ACP)

ObjectiveNanomaterials with superior properties such as high surface area over volume ratio are widely used in dentistry and medicine. This in vitro study was performed to synthesize and characterize nano bioactive glass (nBG) and to evaluate the effect of casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) containing nBG (CPP-ACP@nBG) on enamel remineralization by its application to pH-cycled, synthetically demineralized enamel surfaces.Materials and methodsnBG particles were prepared by sol-gel method. X-ray diffraction pattern (XRD), Fourier-transform infrared spectroscopy (FTIR) and transmittance electron microscopy (TEM) were used for nBG characterization. Synthetic CPP-ACP paste was prepared and nBG particles were added to it. To evaluate the degree of remineralization, 32 healthy human premolars were selected. The samples were randomly divided into 4 groups as: Group 1: Commercial CPP-ACFP (MI paste plus), Group 2: Synthetic casein phosphopeptide-amorphous calcium phosphate containing fluoride (CPP-ACP@F), Group 3: Synthetic CPP/ACP containing nBG (CPP-ACP@nBG), and Group 4: Control (received no treatment). The pastes were then applied on the tooth surfaces for 28 days. The Vickers microhardness of enamel surfaces was evaluated, and enamel surface morphology was assessed using scanning electron microscopy (SEM).ResultsX-Ray diffraction pattern (XRD) of the synthesized nBG show its crystalline nature with the Larnite crystalline mode. Transmittance electron microscope (TEM) microimage of the synthesized nBG shows its formation as less that 100 nm spherical nanoparticle with partial agglomeration. Fourier transform infrared spectroscopy (FTIR) confirm the success formation of nBG with high purity. The results of this study showed that microhardness of the experimental groups was significantly higher than the control group (p ≥ 0.05). SEM images showed a layer of hydroxyapatite in the CPP-ACP@nBG, synthetic and commercial CPP-ACP@F remineralized groups.ConclusionThe results of this study demonstrated that CPP-ACP@F and CPP-ACP@nBG remineralize the surface of the demineralized enamel. Microhardness of the remineralized enamel in the CPP-ACP@nBG group was higher than synthetic and commercial CPP-ACP@F groups.

Preparation and properties of nano silica-based bioactive glass/apatite/sodium alginate composite hydrogel

In this paper, given the lack of osteogenic activity of sodium alginate (SA) hydrogel and to simulate the composition of natural bone, ionic-crosslinking NBG/n-HA/SA hydrogel scaffolds were prepared by using nano bioactive glass (NBG) and nano hydroxyapatite (n-HA) with high bioactivity as composite calcium sources and reinforcement phases, and D-gluconic acid δ-lactone (GDL) as the coagulant. The results showed that the mixture of the precursor forming the network had good injectability and plasticity. When the dosage of GDL was 0.75 g, the gelling time of the composite hydrogel could be regulated within 4–8 min, and the hydrogel had high compressive strength (170–220 kPa), as well. When the mass ratio of calcium source to SA was 1:1, the crosslinking network was relatively uniform with a considerable number of large pores around 40 μm in the structure. In the immersion experiment in vitro, it was found that the composite hydrogel could promote the deposition of bone-like apatite on the material's surface. Meanwhile, the cell experiments in vitro verified that the NBG/n-HA/SA composite hydrogel had good cytocompatibility without cytotoxicity. Moreover, the composite hydrogel could enhance the activity of ALP of mouse bone marrow mesenchymal stem cells, and thus, it had good osteogenic activity.

Multifunctional organic and inorganic hybrid bionanocomposite of chitosan/poly(vinyl alcohol)/nanobioactive glass/nanocellulose for bone tissue engineering

The present study explored a novel organic-inorganic hybrid CPBNC bionanocomposite by developing chitosan (C)-poly(vinyl alcohol) (P)/nanobioactive glass (B)-nanocellulose (NC) with the addition of 1%, 2% and 3 wt% of nanocellulose as template material for bone tissue application. Nanobioactive glass of size 6–10 nm and nanocellulose of size 6–7 nm was confirmed by TEM analysis. X-ray diffraction and Fourier transform infrared spectroscopy indicated strong electrostatic interactions between the functional groups present in the CPBNC bionanocomposite. The mechanical analysis confirmed the formation of CPBNC bionanocomposite and showed improved tensile strength (59.7 ± 1.5 MPa) young's modulus (174.9 ± 6.1 MPa) and compressive strength (4.9 ± 0.2 MPa). Porosity percentage of 61–79% was comparable to cancellous bones with suitable swelling and decreased degradation behaviour properties that could be ideal for cell seeding. Morphological studies by FE-SEM displayed a homogeneous dispersion and smooth surface. The biomimetic mineralization process confirmed the hydroxyapatite nucleation from FE-SEM analysis. It was observed that the CPBNC bionanocomposites provided a better antibacterial effect against E. coli and S. aureus. The hemocompatibility test proved that CPBNC bionanocomposites are blood compatible and showed a hemolytic ratio of less than 2%. The above findings point to a simple method of synthesizing high-performance NC-based scaffolds for bone tissue engineering.

In-Vitro Degradation Behaviors of Composite Scaffolds Based on Poly(Lactide-co-Glycolide-co-ε-Caprolactone), 1,4-Butanediamine Modified Poly(Lactide-co-Glycolide) and Bioceramics

In this work a novel type of composite scaffolds based on poly(lactide-co-glycolide-co-ε-caprolactone) (PLLGC), 1,4-butanediamine modified poly(lactide-co-glycolide) (BMPLGA), nanobioactive glass (NBAG) and β-tricalcium phosphate (β-TCP) were fabricated by using a thermally induced phase separation (TIPS) method. The in-vitro degradation behaviors were investigated by immersing the scaffolds in phosphate buffered saline (PBS, pH = 7.27) solution at 37 °C for 40 days. The properties, including the PBS pH value change and the water uptake, mass loss and morphology changes of the composite scaffolds, were investigated by comparing with pure PLLGC/BMPLGA scaffolds. The introduction of NBAG and β-TCP nanoparticles decreased the degradation rate of the PLLGC/BMPLGA matrix and improved the wetting behavior. The decrease in the degradation rate of the composite scaffolds correlated well with the results obtained from mass loss, water uptake and pH measurements. The degradation rate of the PLLGC/BMPLGA polymer in the composite scaffolds decreased as a result of the alkaline effect of the NBAG and β-TCP particles, with the OH- ions formed neutralizing acidic polymeric degradation products and binding the H+ ions from the tissue fluids.

Preparation and characterization of 3D nanocomposite scaffold from bioactive glass/β-tricalcium phosphate via Robocasting method for bone tissue engineering

In this research, a three-dimensional 45S5 bioactive glass (BG) /β-tricalcium phosphate (TCP) composite (50/50 wt.%) scaffold was prepared by the Robocasting method. For this aim, BG and TCP were synthesized via sol-gel and precipitation methods, respectively, and characterized. The scaffolds were robocast by extruding the ink composed of a proper amount of BG, TCP, and required additives, then, characterized in terms of physicochemical and biological properties. Results showed that nano BG and TCP were synthesized successfully. Scaffold characterization showed that the scaffold had a controlled and interconnected porosity (40%) that exhibited notable average mechanical strength (∼17.39MP) as well as good bioactivity and supported the attachment and the proliferation of mesenchymal stem cells and had a limited effect on the survival of these cells. According to the results, it is concluded that using the Robocasting method for preparing BG/TCP scaffold provided a 3D porous interconnected structure with notable mechanical strength

Bone formation with high bacterial inhibition and low toxicity behavior by melding of Al2O3 on nanobioactive glass ceramics via sol-gel process

Bone formation with high bacterial inhibition and low toxicity behavior by melding of Al2O3 on nanobioactive glass ceramics via sol-gel process

Nano-bioactive glass incorporated polymeric apatite/tricalcium phosphate cement composite supports proliferation and osteogenic differentiation of human adipose-derived stem/stromal cells

Apatite/Tricalcium phosphate composite cement composed with polyacrylic acid (PAA-apatite/TCP) has previously been reported to be a great promise for orthopedic applications. However, it was investigated that PAA could inhibit apatite phase conversion and result in poor bioactivity. To improve those limitations, PAA-apatite/TCP cement modified with the bioactive glass nanoparticle (0–1.5 wt%) was investigated for physical properties, phase formation after setting and bioactivity. In addition, human Adipose-derived Stem/Stromal cells (hASCs), which were isolated from human adipose tissue and represent a widely implemented cell type for tissue engineering applications, were selected to determine their biological response to the bioactive glass modified PAA-apatite/TCP cement. The results indicated that the PAA-apatite/TCP cement added with bioactive glass cement decreased setting time and enhanced apatite phase transformation and bioactivity, as compared with the control cement. For in vitro testing, hASCs viability, proliferation, and differentiation potential were assessed under two cell culture conditions. In details, cells were either cultured with cement-preconditioned medium (indirect setting) or with cement (direct setting). The indirect culture presented a lower proliferation rate as compared with the control medium. In contrast, the result of direct culture indicated a higher proliferation rate on both control cement and 1 wt% bioactive glass incorporated cement, as compared with coverslip control. Moreover, the increase in Alkaline Phosphatase activity following osteogenic stimuli indicated that both cements supported osteogenic commitment. In conclusion, these in vitro data lay the basis for a deeper investigation of 1 wt% bioactive glass incorporated cement as a promising formula for clinical applications in bone engineering and orthopedics.

Nano zinc oxide and nano bioactive glass reinforced chitosan/poly(vinyl alcohol) scaffolds for bone tissue engineering application

The present study was to develop a hybrid chitosan-based bionanocomposite for potential bone tissue engineering applications. Chitosan (C)/Poly(vinyl alcohol) (P)/nano bioactive glass (B)/nano Zinc Oxide (Z) were fabricated by sol-gel assisted solvent casting method. In this method, several CPBZ nanocomposites have been studied by varying the ratios of nano ZnO (0.05%, 0.1%, 0.2%) to yield CPBZ1, CPBZ2 and CPBZ3 hybrid scaffolds. TEM, FESEM- EDAX, XRD and FTIR analyses were performed to characterize the macrostructure of CPBZ bionanocomposites. Nano ZnO of size 20 nm and nano bioactive glass of size 6–10 nm was synthesized and characterized by TEM analysis. The in vitro bioactivity studies confirmed the formation of apatite minerals that results in direct bone bonding implant. SEM revealed the macroporous structure with a pore size of about 10 µm and hydrophilic rough surface. The phase composition of nano ZnO embedded in CPBZ scaffolds was examined by XRD. The characteristic functional groups and the chemical interactions associated with the organic-inorganic phase were analyzed by FTIR. The results of mechanical studies by a universal testing machine (UTM) demonstrated an increase in the tensile strength and apparent density after the addition of nano bioactive glass and nano ZnO. The integration of nano Zinc Oxide in the polymer matrix increased the swelling ratio up to 298% and maintained the delayed biodegradation behavior around 38%, while the pH remained neutral (7.4). The antibacterial activity evaluated by Salmonella typhi and Enterococcus faecalis pathogens showed a better zone of inhibition for gram positive E. faecalis. The hemocompatibility study proves that the CPBZ nanocomposites are blood compatible and showed a hemolytic ratio of less than 2%. The results demonstrated that the prepared bionanocomposites could act as an extracellular matrix in osteogenic tissue engineering.

Effect of Ce-doped bioactive glass/collagen/chitosan nanocomposite scaffolds on the cell morphology and proliferation of rabbit’s bone marrow mesenchymal stem cells-derived osteogenic cells

BackgroundCerium-containing materials have wide applications in the biomedical field, because of the mimetic catalytic activities of cerium. The study aims to deeply estimate the biocompatibility of different scaffolds based on Ce-doped nanobioactive glass, collagen, and chitosan using the first passage of rabbit bone marrow mesenchymal stem cells (BM-MSCs) directed to osteogenic lineage by direct and indirect approach. One percentage of glass filler was used (30 wt. %) in the scaffold, while the percentage of CeO2 in the glass was ranged from 0 to 10 mol. %. Cytotoxicity was evaluated by monitoring of cell morphological changes and reduction in cell proliferation activity of BMMSCs maintained under osteogenic condition using proliferation assays, MTT assay for the direct contact of cells/scaffolds twice in a week, trypan blue and hemocytometer cell counting for indirect contact of cells/scaffolds extracts at day 7. Cell behaviors growth, morphology characteristics were monitored daily under a microscope and cell counting were conducted after 1 week of the incubation of the cells with the extracts of the four composite scaffolds in the osteogenic medium at the end of the week. ResultsShowed that at 24 h after direct contact with composite scaffold, all scaffolds showed proliferation of cells > 50% and increased in cell density on day 7. The scaffold of the highest percentage of CeO2 in bioactive glass nanoparticles (sample CL/CH/C10) showed the lowest inhibition of cell proliferation (< 25%) at day 7. Moreover, the indirect cell viability test showed that all extracts from the four composite scaffolds did not demonstrate a toxic effect on the cells (inhibition value < 25%). ConclusionThe addition of CeO2 to the glass composition improved the biocompatibility of the composite scaffold for the proliferation of rabbit bone marrow mesenchymal stem cells directed to osteogenic lineage.

Effectiveness of Nano Bioactive Glass Fiber Loaded with Platelet-Rich Plasma on Thermal Wound Healing Process in Rats.

In this study we evaluated the impact of topical application of bioactive glass fibers loaded PRP on a deep seconddegree thermal wound and its healing process sub-streaming molecular pathway of re-epithelialization. Wistar rats were randomly divided into four groups: normal control group, model group (deep second-degree thermal wound), PRP group, and PRP+nanobioactive glass fiber group. After treatment, the changes of wounds were observed daily. H&E staining was used to evaluate the pathological changes and also, qRT-PCR was used to detect the mRNA expression of KGF, IL-1, IL-6, IL-10, TGF-β, EGF, VEGF, HIF-1α, integrin α3 and integrin β1 in wound tissues. In the current study, we observed that PRP group and the PRP group basically re-epithelized on the 21st day. The wound healing rates of the PRP+nanobioactive glass fiber group and PRP group at each time point were higher than those in the model group, while there was no significant difference in wound healing rate between the PRP+nanobioactive glass fiber group and PRP group at each time point. H&E staining showed that the pathological scores of skin wound repairing in the PRP+nanobioactive glass fiber group on the 7th, 14th and 21st day were higher than that of in the model group. The qPCR results suggested the mRNA expression of IL-1, IL-6 and IL-10 in the PRP+nanobioactive glass fiber group and the PRP group were lower than those in the untreated group on the 14th day; the expression of VEGF and EGF mRNA were higher on the 3rd day; the mRNA expression of TGF-β, HIF-1α showed a tendency of increasing first and decreasing then; integrin β1 mRNA expression increased significantly, which was highest; integrin α3 mRNA expression was higher on day 3rd and 21th, respectively. The PRP+nanobioactive glass fibers and PRP can shorten the wound healing time and improve the healing quality mainly by promoting the wound epithelization through increasing the expression of EGF, VEGF, TGF-β, HIF-1α, Integrin α3, and meanwhile increasing the release of Integrin β1 and other mechanisms.