Bioactive Glass-ceramic Scaffolds Research Articles

Silver-doped glass-ceramic scaffolds with antibacterial and bioactive properties for bone substitution

The preparation of scaffolds that are both macroporous and mechanically strong is a significant challenge in the development of bioactive ceramic materials for bone substitution. Furthermore, the introduction of beneficial extra-functionalities such as bacterial inhibition is highly appealing but adds complexity to implant design and production. In this study, we aimed to fabricate highly porous, bioactive and antibacterial glass-ceramic scaffolds with interconnected macropores through the foam replica method. The scaffolds were sintered at two different temperatures (620 and 850 °C), yielding glassy or partially crystallized materials, respectively. The scaffold produced at higher temperature was found to be highly porous (>75 vol%), mechanically stronger and able to induce hydroxyapatite formation after three days of soaking in SBF (in vitro bioactivity). In order to confer antibacterial activity, silver (Ag) ions were introduced onto the scaffold surface through ion exchange in an aqueous solution. Compositional analysis confirmed the successful doping of the scaffold surface with silver, which was continuously released in SBF for at least 28 days, as revealed by ICP-MS. Finally, the antibacterial action of the Ag-doped scaffold was confirmed towards Staphylococcus epidermidis. Overall, the results reported in this work show the potential of foam-like Ag-doped bioactive glass-ceramic scaffolds to be used in applications requiring bone substitution and antibacterial properties.

Micro-CT imaging and finite element models reveal how sintering temperature affects the microstructure and strength of bioactive glass-derived scaffolds

This study focuses on the finite element simulation and micromechanical characterization of bioactive glass-ceramic scaffolds using Computed micro Tomography (μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}CT) imaging. The main purpose of this work is to quantify the effect of sintering temperature on the morphometry and mechanical performance of the scaffolds. In particular, the scaffolds were produced using a novel bioactive glass material (47.5B) through foam replication, applying six different sintering temperatures. Through μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}CT imaging, detailed three-dimensional images of the scaffold’s internal structure are obtained, enabling the extraction of important geometric features and how these features change with sintering temperature. A finite element model is then developed based on the μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}CT images to simulate the fracture process under uniaxial compression loading. The model incorporates scaffold heterogeneity and material properties—also depending on sintering temperature—to capture the mechanical response, including crack initiation, propagation, and failure. Scaffolds sintered at temperatures equal to or higher than 700 ∘\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{\\circ }$$\\end{document}C exhibit two-scale porosity, with micro and macro pores. Finite element analyses revealed that the dual porosity significantly affects fracture mechanisms, as micro-pores attract cracks and weaken strength. Interestingly, scaffolds sintered at high temperatures, the overall strength of which is higher due to greater intrinsic strength, showed lower normalized strength compared to low-temperature scaffolds. By using a combined strategy of finite element simulation and μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}CT-based characterization, bioactive glass-ceramic scaffolds can be optimized for bone tissue engineering applications by learning more about their micromechanical characteristics and fracture response.

The role of (HCO3)− ions in SBF on the interaction with bioactive glass-ceramic scaffold

Simulated Body Fluid (SBF) has concentrations of inorganic elements nearly equal to those of human blood plasma (BP). However, there are some differences between SBF and BP which can distort the results of in vitro bioactivity tests. Contrary to BP, SBF has a too low concentration of (HCO3)- ions (only 4 instead of 27 mmol·dm−3) and on the contrary a higher concentration of Cl− ions (introduced by the TRIS-HCl buffer). Indeed, the main difference between SBF and BP is the presence of the TRIS buffer in SBF which is used for neutral pH maintaining. The aim of this work was to study the effect of (HCO3)- ions in non-buffered SBF on the solubility of a bioactive glass-ceramic material and the formation of a new phase on the sample surface. A highly reactive glass-ceramic scaffold derived from 45S5 bioactive glass was tested under static-dynamic conditions using SBF solution with different (HCO3)- ion concentrations (4, 20 and 27 mmol·dm−3). The results were compared with data obtained using standardized buffered SBF solution. A non-buffered SBF solution with a concentration of (HCO3)- ions closer to the real concentration in BP was shown to have the potential to replace the standardized SBF solution since the ISO 23317:2014 using SBF can give false-positive results of in vitro bioactivity tests.

Bioactive Glass-Ceramic Scaffolds Coated with Hyaluronic Acid-Fatty Acid Conjugates: A Feasibility Study.

Promoting bone healing is a key challenge in our society that can be tackled by developing new implantable biomaterials provided with regenerative properties. In this work, the coating of three-dimensional porous glass-derived scaffolds with hyaluronic acid (HA)-fatty acids was investigated for the first time. The starting scaffolds, based on bioactive silicate glass, were produced by foam replication followed by sintering; then, HA-palmitate and HA-oleate conjugate coatings were deposited on the scaffold struts through a dipping procedure. FT-IR analysis confirmed the successful deposition of the coatings on the surface and struts of the scaffolds, the foam-like architecture of which was maintained as assessed by SEM investigations. The in vitro bioactivity of the HA-fatty-acid-coated scaffolds was studied by immersion tests in simulated body fluid and the subsequent evaluation of hydroxyapatite formation. The deposition of the polymeric coating did not inhibit the apatite-forming ability of scaffolds, as revealed by the formation of nanostructured hydroxyapatite agglomerates 48 h from immersion. These promising results motivate further investigation of these novel bioactive systems, which are expected to combine the bone-bonding properties of the glass with the wound-healing promotion carried out by the polymeric conjugates.

Bioactive SiO2-K2O-CaO-P2O5 glass-ceramic scaffold prepared using polyurethane foam template

A glass-ceramic in the SiO2-K2O-CaO-P2O5 quaternary system was prepared by substituting the Na2O component with K2O to avoid Na2Ca2Si3O9 formation upon thermal treatment since this phase decreases apatite formation kinetics on glass material. To form the glass-ceramic, a modified sol-gel method involving solution precipitation, followed by reagents encapsulation in citric acid was adopted to enable the use of sodium metasilicate as a cheap substitute for traditional alkoxysilane silica precursors. The foam replication method using polyurethane foam as a sacrificial template was used to obtain the scaffold, which on analysis gave a porosity of 92% and an average pore size of 36±6 mm. In vitro bioactivity evaluation in simulated body fluid for a maximum of 14 days indicated the formation of hydroxyapatite on the sample surface. Phase analysis showed that CaSiO3 and K2CaSiO4 crystals formed in the sintered sample as the main phases, which exhibited biodegradability in simulated body fluid (SBF). Therefore, economically-derived porous bioactive glass-ceramic scaffolds based on the current method (a simple process) are feasible.

A 3D-printed molybdenum-containing scaffold exerts dual pro-osteogenic and anti-osteoclastogenic effects to facilitate alveolar bone repair

The positive regulation of bone-forming osteoblast activity and the negative feedback regulation of osteoclastic activity are equally important in strategies to achieve successful alveolar bone regeneration. Here, a molybdenum (Mo)-containing bioactive glass ceramic scaffold with solid-strut-packed structures (Mo-scaffold) was printed, and its ability to regulate pro-osteogenic and anti-osteoclastogenic cellular responses was evaluated in vitro and in vivo. We found that extracts derived from Mo-scaffold (Mo-extracts) strongly stimulated osteogenic differentiation of bone marrow mesenchymal stem cells and inhibited differentiation of osteoclast progenitors. The identified comodulatory effect was further demonstrated to arise from Mo ions in the Mo-extract, wherein Mo ions suppressed osteoclastic differentiation by scavenging reactive oxygen species (ROS) and inhibiting mitochondrial biogenesis in osteoclasts. Consistent with the in vitro findings, the Mo-scaffold was found to significantly promote osteoblast-mediated bone formation and inhibit osteoclast-mediated bone resorption throughout the bone healing process, leading to enhanced bone regeneration. In combination with our previous finding that Mo ions participate in material-mediated immunomodulation, this study offers the new insight that Mo ions facilitate bone repair by comodulating the balance between bone formation and resorption. Our findings suggest that Mo ions are multifunctional cellular modulators that can potentially be used in biomaterial design and bone tissue engineering.

Role of molybdenum in material immunomodulation and periodontal wound healing: Targeting immunometabolism and mitochondrial function for macrophage modulation

Recently, strategies that can target the underlying mechanisms of phenotype change to modulate the macrophage immune response from the standpoint of biological science have attracted increasing attention in the field of biomaterials. In this study, we printed a molybdenum-containing bioactive glass ceramic (Mo-BGC) scaffold as an immunomodulatory material. In a clinically relevant critical-size periodontal defect model, the defect-matched scaffold featured robust immunomodulatory activity, enabling long-term stable macrophage modulation and leading to enhanced regeneration of multiple periodontal tissues in canines. Further studies demonstrated that the regeneration-enhancing function of Mo-BGC scaffold was macrophage-dependent by using canines with host macrophage depletion. To investigate the role of Mo in material immunomodulation, in vitro investigations were performed and revealed that Mo-BGC powder extract, similar to MoO42−-containing medium, induced M2 polarization by enhancing the mitochondrial function of macrophages and promoted a cell metabolic shift from glycolysis toward mitochondrial oxidative phosphorylation. Our findings demonstrate for the first time an immunomodulatory role of a Mo-containing material in the dynamic cascade of wound healing. By targeting the immunometabolism and mitochondrial function of macrophages, Mo-mediated immunomodulation provides new avenues for future material design in the field of tissue engineering and regenerative medicine.

LZS bioactive glass-ceramic scaffolds: Colloidal processing, foam replication technique and mechanical properties to bone tissue engineering

Scaffolds are used in bone replacement because present biocompatibility, three-dimensional structure, and high porosity. However, despite the efforts, there are still significant barriers to the development of reliable, synthetic scaffolds to repair large defects is one of the challenges of regenerative medicine. Therefore, innovative solutions are needed better to meet the requirements of a minimally invasive approach while providing adequate vascularity and strength and mechanical reliability. In this sense, the obtainment of a material that satisfies all these requirements is very important. This work aims to evaluate the mechanical properties of glass-ceramic scaffolds of the LZS (Li2O–ZrO2–SiO2) system produced by the replica method. For this, detailed colloidal processing was carried out to identify the solids content, amount of dispersant, and the binder most suitable to produce scaffolds. Finally, the mechanical reliability of the most suitable composition was evaluated by Weibull statistics. Suspensions containing 47 vol% of LZS relative to glass and 0.2 wt % of dispersant were used. In addition, dispersion times and the amount of binder were adjusted. Scaffolds of bioactive glass-ceramics were obtained at 900 °C, replicating polyurethane foams. Then they were morphologically, structurally, and mechanically characterized. The obtained bioactive glass-ceramic scaffolds presented porosity up to 83%, compressive strengths comparable to those of trabecular bone, up to 1.3 MPa, in addition to pore size >300 μm, desirable to favor biological interests destined to the regeneration and formation of bone tissue, demonstrating the possibility of its use as a material for bone replacement or filling. The Weibull modulus found for the glass-ceramic scaffolds produced is 4.18: within the expected range of mechanical reliability for application in bone regeneration.

The effect of Ag incorporation on the characteristics of the polymer derived bioactive silicate phosphate glass-ceramic scaffolds

In the bone tissue engineering field (BTE), it is of significant importance to develop bioactive multifunctional scaffolds with enhanced osteoconductivity, osteoinductivity, and antibacterial properties required for lost bone tissue regeneration. In this work, a bioactive glass-ceramic scaffold was manufactured via a novel polymer-derived ceramics (PDC) manufacturing method. To gain antibacterial properties, the silver ions were incorporated in controlled amount along with other precursors in the PDC processing stage. Microstructural and structural properties of the fabricated silicate-phosphate glass-ceramic scaffold were evaluated by scanning electron microscopy (SEM) equipped with energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD) analysis, respectively. Furthermore, bioactivity, antibacterial, and cytotoxicity evaluation of PDC scaffolds were conducted. The microstructural analysis determined that scaffolds have interconnected porous network with two different pore range size favorable for osteointegration and bone formation. The structural analysis confirmed that fabricated glass-ceramic scaffolds contain bioactive octacalcium phosphate (OCP) phase responsible for enhanced bioactivity and HCA formation during the immersing of scaffolds in simulated body fluid (SBF) for several days. Moreover, PDC scaffolds with Ag nanoparticles showed considerable antibacterial properties against Gram-negative Klebsiella pneumoniae and Gram-positive Staphylococcus aureus bacteria cells. This study has demonstrated that it is possible to develop a novel group of antibacterial and bioactive Ag incorporated silicate-phosphate glass-ceramic scaffolds for BTE applications, such that, it was verified in vivo.

Glass powders and reactive silicone binder: Application to digital light processing of bioactive glass-ceramic scaffolds

Powdered ‘silica-defective glasses’, mixed with silicones, have been already shown as a promising solution for the sintering, in air, of glass-ceramics with complex geometries. A fundamental advantage of the approach is the fact silicones act as binders up to the firing temperature, at which they transform into silica. A specified ‘target’ glass-ceramic formulation is achieved through the interaction between glass powders and the binder-derived silica. The present paper is dedicated to the extension of the approach to the digital light processing of reticulated glass-ceramic scaffolds, for tissue engineering applications, starting from glass powders suspended in an engineered photocurable silicone-based binder. The silicone component, besides providing an extended binding action up to the maximum firing temperature, stabilizes the 3D-printed shapes during sintering. The formation of a rigid silica skeleton, from the transformation of the silicone binder, prevents from excessive viscous flow of softened glass. The final phase assemblage does not depend simply on glass devitrification but also on the glass/silica skeleton interaction.

Elastic Mechanical Properties of 45S5-Based Bioactive Glass-Ceramic Scaffolds.

Porosity is recognized to play a key role in dictating the functional properties of bioactive scaffolds, especially the mechanical performance of the material. The mechanical suitability of brittle ceramic and glass scaffolds for bone tissue engineering applications is usually evaluated on the basis of the compressive strength alone, which is relatively easy to assess. This work aims to investigate the porosity dependence of the elastic properties of silicate scaffolds based on the 45S5 composition. Highly porous glass–ceramic foams were fabricated by the sponge replica method and their elastic modulus, shear modulus, and Poisson’s ratio were experimentally determined by the impulse excitation technique; furthermore, the failure strength was quantified by compressive tests. As the total fractional porosity increased from 0.52 to 0.86, the elastic and shear moduli decreased from 16.5 to 1.2 GPa and from 6.5 to 0.43 GPa, respectively; the compressive strength was also found to decrease from 3.4 to 0.58 MPa, whereas the Poisson’s ratio increased from 0.2692 to 0.3953. The porosity dependences of elastic modulus, shear modulus and compressive strength obeys power-law models, whereas the relationship between Poisson’s ratio and porosity can be described by a linear approximation. These relations can be useful to optimize the design and fabrication of porous biomaterials as well as to predict the mechanical properties of the scaffolds.

Fabrication and multiscale characterization of 3D silver containing bioactive glass-ceramic scaffolds

In this work, we fabricated and characterized bioactive 3D glass-ceramic scaffolds with inherent antibacterial properties. The sol-gel (solution-gelation) technique and the sacrificial template method were applied for the fabrication of 3D highly porous scaffolds in the 58.6SiO2 - 24.9CaO - 7.2P2O5 - 4.2Al2O3 – 1.5Na2O −1.5K2O – 2.1Ag2O system (Ag-BG). This system is known for its advanced bioactive and antibacterial properties. The fabrication of 3D scaffolds has potential applications that impact tissue engineering. The study of the developed scaffolds from macro-characteristics to nano-, revealed a strong correlation between the macroscale properties such as antibacterial action, bioactivity with the microstructural characteristics such as elemental analysis, crystallinity. Elemental homogeneity, morphological, and microstructural characteristics of the scaffolds were studied by scanning electron microscopy associated with energy dispersive spectroscopy (SEM-EDS), transmittance electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and UV-visible spectroscopy methods. The compressive strength of the 3D scaffolds was measured within the range of values for glass-ceramic scaffolds with similar compositions, porosity, and pore size. The capability of the scaffolds to form an apatite-like phase was tested by immersing the scaffolds in simulated body fluid (SBF) and the antibacterial response against methicillin-resistant Staphylococcus aureus (MRSA) was studied. The formation of an apatite phase was observed after two weeks of immersion in SBF and the anti-MRSA effect occurs after both direct and indirect exposure.

Glass powders and reactive silicone binder: Interactions and application to additive manufacturing of bioactive glass-ceramic scaffolds

A novel concept for the additive manufacturing of three-dimensional glass-ceramic scaffolds, to be used for tissue engineering applications, was based on fine glass powders mixed with a reactive binder, in the form of a commercial silicone. The powders consisted of ‘silica-defective glass’ specifically designed to react, upon firing in air, with the amorphous silica yielded by the binder. By silica incorporation, the glass was intended to reach the composition of an already known CaOsingle bondNa2Osingle bondB2O3single bondSiO2 system. Silica from the binder provided up to 15 wt% of the total silica. With the same overall formulation, silicone-glass powder mixtures led to nearly the same phase assemblage formed by the reference system, crystallizing into wollastonite (CaSiO3) and Ca-borate (CaB2O4). Samples from silicone-glass powder mixtures exhibited an excellent shape retention after firing, which was later exploited in highly porous reticulated scaffolds, obtained by means of direct ink writing (DIW).

Digital light processing of wollastonite-diopside glass-ceramic complex structures

In this work, the possibility of shaping a glass-filled photosensitive polymer resin with Digital Light Processing (DLP) into a complex 3D structure and transforming it subsequently into a bioactive glass-ceramic scaffold was investigated. The influence of the printing conditions and the heat-treatment was studied using a 41 vol% glass-filled acrylated polymer resin. Scaffolds with designed architecture were turned into a wollastonite-diopside glass-ceramic at 1100 °C. They completely maintained their shape, exhibited no viscous flow and showed a homogenous linear shrinkage of around 25%. At 83 vol% porosity structures with Kelvin cell design exhibited a compressive strength exceeding 3 MPa, demonstrating that the material is suitable for the fabrication of bioceramic scaffolds for bone tissue engineering applications.

Bioactive glass-ceramic scaffolds by additive manufacturing and sinter-crystallization of fine glass powders

Abstract

3D-printed scaffolds with bioactive elements-induced photothermal effect for bone tumor therapy

For treatment of bone tumor and regeneration of bone defects, the biomaterials should possess the ability to kill tumor cells and regenerate bone defect simultaneously. To date, there are a few biomaterials possessing such dual functions, the disadvantages, however, such as long-term toxicity and degradation, restrict their application. Although bioactive elements have been incorporated into biomaterials to improve their osteogenic activity, there is no report about elements-induced functional scaffolds for photothermal tumor therapy. Herein, the elements (Cu, Fe, Mn, Co)-doped bioactive glass-ceramic (BGC) scaffolds with photothermal effect and osteogenic differentiation ability were prepared via 3D-printing method. Moreover, the photothermal anti-tumor effect and osteogenic activity of these scaffolds were systematically investigated. The prepared elements-doped scaffolds possessed excellent photothermal performance, which displayed a trend, 5Cu-BGC > 5Fe-BGC > 5Mn-BGC > 5Co-BGC, in this study. The final temperature of elements-doped scaffolds can be well controlled by altering the doping element categories, contents and laser power density. Additionally, the hyperthermia induced by 5Cu-BGC, 5Fe-BGC and 5Mn-BGC effectively killed tumor cells in vitro and inhibited tumor growth in vivo. More importantly, 5Fe-BGC and 5Mn-BGC scaffolds could promote rabbit bone mesenchymal stem cells (rBMSCs) adhesion, and the ionic products released from elements-doped scaffolds significantly stimulated the osteogenic differentiation of bone-forming cells. These results suggested that 5Fe-BGC and 5Mn-BGC scaffolds possessed promising potential for photothermal treatment of bone tumor and at the same time for stimulating bone regeneration, representing a smart strategy for the treatment of bone tumors by combining dual functional bioactive ions with tissue engineering scaffolds. Statement of SignificanceThe major innovation of this study is that we fabricated the elements (Cu, Fe, Mn, Co)-doped bioactive scaffolds via 3D printing technique and found that they possess distinct photothermal performance and osteogenic differentiation ability. To the best of our knowledge, there is no report about elements-doped scaffolds for photothermal therapy of bone tumor. This is an important research advance by combining the photothermal effect and osteogenic differentiation activity of bioactive elements in the scaffold system for potential bone tumor therapy and bone reconstruction. We optimized the elements-doped scaffolds and found the photothermal effect of elements-doped scaffolds (5Cu-BGC, 5Fe-BGC, 5Mn-BGC) could effectively kill tumor cells in vivo. The photothermal performance of elements-doped scaffolds follows a trend: 5Cu-BGC > 5Fe-BGC > 5Mn-BGC > 5Co-BGC > BGC. Compared to traditional nano-sized photothermal agents, bioactive elements-induced functional scaffolds have better biosecurity and bioactivity. Furthermore, 5Fe-BGC and 5Mn-BGC scaffolds displayed excellent bone-forming activity by stimulating the osteogenic differentiation of bone-forming cells. The major significance of the study is that the elements-doped bioactive glass-ceramics (5Fe-BGC, 5Mn-BGC) have great potential to be used as bifunctional scaffolds for photothermal tumor therapy and bone regeneration, representing a smart strategy for the treatment of bone tumors by combining dual functional bioactive ions with tissue engineering scaffolds.

Bioactive Glass-Ceramic Foam Scaffolds from 'Inorganic Gel Casting' and Sinter-Crystallization.

Highly porous bioactive glass-ceramic scaffolds were effectively fabricated by an inorganic gel casting technique, based on alkali activation and gelification, followed by viscous flow sintering. Glass powders, already known to yield a bioactive sintered glass-ceramic (CEL2) were dispersed in an alkaline solution, with partial dissolution of glass powders. The obtained glass suspensions underwent progressive hardening, by curing at low temperature (40 °C), owing to the formation of a C–S–H (calcium silicate hydrate) gel. As successful direct foaming was achieved by vigorous mechanical stirring of gelified suspensions, comprising also a surfactant. The developed cellular structures were later heat-treated at 900–1000 °C, to form CEL2 glass-ceramic foams, featuring an abundant total porosity (from 60% to 80%) and well-interconnected macro- and micro-sized cells. The developed foams possessed a compressive strength from 2.5 to 5 MPa, which is in the range of human trabecular bone strength. Therefore, CEL2 glass-ceramics can be proposed for bone substitutions.

3D printing of Mo-containing scaffolds with activated anabolic responses and bi-lineage bioactivities.

When osteochondral tissues suffer from focal or degenerative lesions caused by trauma or disorders, it is a tough challenge to regenerate them because of the limited self-healing capacity of articular cartilage. In this study, a series of Mo-doped bioactive glass ceramic (Mo-BGC) scaffolds were prepared and then systematically characterized. The released MoO42- ions from 7.5Mo-BGC scaffolds played a vital role in regenerating articular cartilage and subchondral bone synchronously.Methods: The Mo-BGC scaffolds were fabricated through employing both a sol-gel method and 3D printing technology. SEM, EDS, HRTEM, XRD, ICPAES and mechanical strength tests were respectively applied to analyze the physicochemical properties of Mo-BGC scaffolds. The proliferation and differentiation of rabbit chondrocytes (RCs) and human bone mesenchymal stem cells (HBMSCs) cultured with dilute solutions of 7.5Mo-BGC powder extract were investigated in vitro. The co-culture model was established to explore the possible mechanism of stimulatory effects of MoO42- ions on the RCs and HBMSCs. The efficacy of regenerating articular cartilage and subchondral bone using 7.5Mo-BGC scaffolds was evaluated in vivo.Results: The incorporation of Mo into BGC scaffolds effectively enhanced the compressive strength of scaffolds owing to the improved surface densification. The MoO42- ions released from the 7.5Mo-BGC powders remarkably promoted the proliferation and differentiation of both RCs and HBMSCs. The MoO42- ions in the co-culture system significantly stimulated the chondrogenic differentiation of RCs and meanwhile induced the chondrogenesis of HBMSCs. The chondrogenesis stimulated by MoO42- ions happened through two pathways: 1) MoO42- ions elicited anabolic responses through activating the HIF-1α signaling pathway; 2) MoO42- ions inhibited catabolic responses and protected cartilage matrix from degradation. The in vivo study showed that 7.5Mo-BGC scaffolds were able to significantly promote cartilage/bone regeneration when implanted into rabbit osteochondral defects for 8 and 12 weeks, displaying bi-lineage bioactivities.Conclusion: The 3D-printed Mo-BGC scaffolds with bi-lineage bioactivities and activated anabolic responses could offer an effective strategy for cartilage/bone interface regeneration.

Bioactivity, mechanical properties and drug delivery ability of bioactive glass-ceramic scaffolds coated with a natural-derived polymer

In this work, hybrid melanin-coated bioactive glass-ceramic multifunctional scaffolds were developed and characterized in terms of mechanical strength, in vitro bioactivity in simulated body fluid (SBF) and ability to load ibuprofen. The coated scaffolds exhibited an accelerated bioactivity in comparison with the uncoated ones, being able of developing hydroxyapatite-like crystals after 7days soaking in simulated body fluid (SBF). Besides its positive influence on the scaffolds bioactivity, the melanin coating was able to enhance their mechanical properties, increasing the initial compressive strength by a factor of >2.5. Furthermore, ibuprofen was successfully loaded on this coating, allowing a controlled drug release of the anti-inflammatory agent.

Bioactive glass-ceramic scaffolds: Processing and properties

Abstract