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This study investigated the impact of some specific experimental calcium phosphate cements doped with different fluoride salts (FDCPCs) concentrations on the basal functions of human Dental Pulp Stem Cells (hDPSCs). Furthermore, this study also examined the migration, as well as the mineralisation through osteogenic differentiation. Experimental FDCPCs were formulated using different concentrations of calcium/sodium fluoride salts [(5 wt%: VS5F), (10 wt%: VS10F), (20 wt%: VS20F)]. A fluoride-free calcium phosphate (VS0F) was used as a control. The hDPSCs were assessed to evaluate their self-renewal and migration activity in the presence of eluates of the different FDCPCs. A viability assay in osteogenic conditions was carried out, along with the differentiation potential through Alkaline Phosphatase Activity (ALP), and Alizarin Red Staining (ARS). Moreover, the gene expression of specific markers (RUNX2, ALP, COL1α1, OCN, OPN, DSPP, MEPE, and DMP-1) was also evaluated. All the tested FDCPD had no influence on cell migrations, but they caused a decrease in cell viability in osteogenic conditions when not diluted. Conversely, the eluants of VS20F showed a positive effect on stem cell differentiation. This result was corroborated through ALP activity, ARS assay. Moreover, upregulation of specific gene markers such as RUNX2, DMP-1, and DSPP was observed in hDPSCs, especially when treated with VS20F. The experimental FDCPC tested in this study exhibits a dose-dependent capacity to promote mineralisation in osteogenic environment. The FDCPC-VS20F seems to be the most promising experimental material suitable for developing of pulp-capping materials with osteogenic and bioactive properties. • The experimental fluoride-doped calcium phosphate cements exhibit a dose-dependent capacity to promote osteogenesis. • Gene expression markers RUNX2, OCN, and MEPE resulted particularly upregulated in VS20F. • Cells treated with 1:50 dilution extracts exhibited elevated ALP activity on day 7, especially in the presence of VS20F. • The experimental calcium phosphate containing 20 % fluoride may be the most promising cements for pulp-capping application. [ABSTRACT FROM AUTHOR]

Objectives: To evaluate and compare the ion-releasing capability of three different restorative systems at the restoration/tooth interface elemental analysis using energy-dispersive X-ray technique. Additionally, micromorphological patterns of the restoration/tooth interfaces was investigated. Materials and methods: Eighteen freshly extracted sound human premolars were collected for the study. The premolars were randomly assigned into 3 groups (n = 6) based on the type of restorative materials used: Giomer (Beautifill II), ion-releasing composite (Activa Presto), and RMGI (Riva Light Cure). Half of the specimens in each group were tested after 24 h (the "immediate group"), while the remaining half were tested after 6 months of storage in deionized water (the "delayed group"). Standardized box-shaped cavities along the cervical area of teeth crowns and restored them with the assigned restorative material following manufacturers' instructions. The specimens were sectioned buccolingually into 2 halves. One half of each specimen was subjected to elemental analysis using energy-dispersive X-ray technique (EDX), while the remaining half was sputter coated and underwent micromorphological analysis of the restoration/tooth interface using a scanning electron microscope (SEM). The collected data from elemental analysis test were tabulated and subjected to statistical analysis. Results: The two-way ANOVA test showed significant differences in both phosphorus and calcium levels among the tested restorative systems (p < 0.05). In the immediate subgroup, RMGI recorded the highest phosphorus level (0.1527), followed by the ion-releasing composite (0.1172), while Giomer exhibited the least levels (0.0326) (p < 0.05). The ion-releasing composite group had the highest calcium level (0.2797), followed by RMGI (0.248), and Giomer (0.2385) respectively (p < 0.05). In the delayed subgroups, Giomer recorded the highest phosphorus level (0.1526), followed by the ion-releasing composite (0.1058), and RMGI group (0.0466) respectively (p < 0.05). RMGI had the highest calcium level (0.2801), followed by the ion-releasing composite (0.2659), and Giomer had the lowest level (0.1792) (p < 0.05). The micromorphological analysis of the restoration/tooth interfaces showed good adaptation between the composite and tooth substrate in different restorative groups. Conclusions: The ion-releasing capability of the three restorative systems appears to be comparable. The rate of mineral release and diffusion is affected by time and composition. [ABSTRACT FROM AUTHOR]

Abstract Objectives To evaluate and compare the ion-releasing capability of three different restorative systems at the restoration/tooth interface elemental analysis using energy-dispersive X-ray technique. Additionally, micromorphological patterns of the restoration/tooth interfaces was investigated. Materials and methods Eighteen freshly extracted sound human premolars were collected for the study. The premolars were randomly assigned into 3 groups (n = 6) based on the type of restorative materials used: Giomer (Beautifill II), ion-releasing composite (Activa Presto), and RMGI (Riva Light Cure). Half of the specimens in each group were tested after 24 h (the “immediate group”), while the remaining half were tested after 6 months of storage in deionized water (the “delayed group”). Standardized box-shaped cavities along the cervical area of teeth crowns and restored them with the assigned restorative material following manufacturers’ instructions. The specimens were sectioned buccolingually into 2 halves. One half of each specimen was subjected to elemental analysis using energy-dispersive X-ray technique (EDX), while the remaining half was sputter coated and underwent micromorphological analysis of the restoration/tooth interface using a scanning electron microscope (SEM). The collected data from elemental analysis test were tabulated and subjected to statistical analysis. Results The two-way ANOVA test showed significant differences in both phosphorus and calcium levels among the tested restorative systems (p

Objectives: This paper reviews the chemical behaviour of glass polyalkenoate (glass-ionomer) dental cements, both conventional and resin-modified, in contact with natural tissues, with the aim of determining whether these materials can be considered to be bioactive. Data: Relevant papers describing the behaviour of bioactive glasses and ceramics, and glass-ionomer (glass polyalkenoate) cements have been identified using PubMed and Science Direct. This has allowed a comparison to be made between the behaviour of glass-ionomers and the speciality glasses and ceramics that are widely classified as bioactive, a designation considered valid for over fifty years. More recent papers concerning bioactive metals and polymers have also been studied and both in vitro and in vivo studies are included. Sources: Have included general papers on the chemistry and biological behaviour of bioactive glasses and ceramics, as well as papers on glass-ionomers dealing with (i) ion release, (ii) bonding to the surface of teeth, (iii) influence on surrounding pH and (iv) interaction with bone. Conclusion: The literature shows that glass-ionomers (glass polyalkenoates) have three types of behaviour that are similar to those of bioactive glasses as follows: Formation of direct bonds to living tissue (teeth and bones) without fibrous capsule; release of biologically beneficial ions; and change of the local pH. However, in in vitro tests, they do not cause calcium phosphate to precipitate from solutions of simulated body fluid, SBF. Despite this, studies show that, in patients, glass-ionomers interact chemically with hard tissues and this suggests that may indeed be considered bioactive.

This study expands the knowledge of bioactive glass S53P4 dissolution by implementing a cascade reactor to a continuous dissolution setup. Three reactors were coupled in a series to study the effects of released ions on S53P4 reactions in each reactor. The pH and ion concentrations were measured in Tris-buffer and simulated body fluid flowing through the cascade reactor for five days. The reaction layer formed on the particles in each reactor were also analysed. In Tris, the dissolved Si decreased from 100% to 40% and 26% in the consecutive reactors after five days. In SBF, Si decreased from 64% to 11% and 8%. Thus, the ions released and decrease of available hydrogen ions for ion exchange influenced the dissolution behaviour of S53P4. The results partly explain the differences in the reaction degree between individual bioactive glass particles used as a bone graft in the same defect site.

Corrosion and metal release characteristics of cobalt-based alloys are important factors influential on their biomedical applications. This study fabricated a porous Vitallium (CoCrMo) alloy and then coated with a 58S bioglass coating by applying the sol-gel dipping method with 3, 4 and 5 cycles to examine the corrosion and ion release performance of this alloy. For this purpose, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and immersion tests were conducted in the simulated body fluid (SBF) at 37 °C. Also, the released ion measurements were performed by inductive coupled plasma optical emission spectrometry (ICP-OES). SEM examinations on the porous substrate indicated that this porous scaffold exhibited the porosity of 37% and the content of small porosities was decreased; however, the macrospores on the surface were intact after applying bioglass coatings. Furthermore, increasing the dipping cycles led to enhancing the corrosion potential from − 191 mV (in the uncoated porous sample) to − 98 mV (in the coated porous sample dipped 5 cycles in the bioglass sols). EIS results in SBF demonstrated that the corrosion performance of the coatings was improved by increasing the dipping cycles from 0 to 5. ICP-OES results also proved that the presence of the 58 S bioglass coating on the porous Vitallium decreased the release of cobalt and chromium ions, while it enriched Ca and P, thereby improving the bioactivity of the samples. [ABSTRACT FROM AUTHOR]

Introduction: Incorporation of calcium phosphate agents into fluoride varnishes might improve anticaries benefits. But when clinical results do not mirror this view, explanations remain unclear. The hypothesis: Our hypothesis is that better clinical outcomes are obtained from fluoride plus calcium phosphate varnishes when there is sustained, controlled release of mineralizing ions. Evaluation of the hypothesis: Calculations of ion activity products and putative mineral phases have been underutilized in assessing clinical outcomes of fluoride varnishes with calcium phosphate agents. In this study, a mineral phase comparison between a low-release varnish comprising functionalized tricalcium phosphate (fTCP) against a high-release varnish comprising casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) was made. These calculations revealed the predominance of hydroxyapatite, fluorapatite, and calcium fluoride formation for the varnish containing fTCP, whereas the varnish containing CPP-ACP produced the same minerals along with β-TCP and octacalcium phosphate. This hypothesis shows the mineral phases expected to form from fluoride plus calcium phosphate varnishes might bear on clinical outcomes.

Introduction: Incorporation of calcium phosphate agents into fluoride varnishes might improve anticaries benefits. But when clinical results do not mirror this view, explanations remain unclear. The hypothesis: Our hypothesis is that better clinical outcomes are obtained from fluoride plus calcium phosphate varnishes when there is sustained, controlled release of mineralizing ions. Evaluation of the hypothesis: Calculations of ion activity products and putative mineral phases have been underutilized in assessing clinical outcomes of fluoride varnishes with calcium phosphate agents. In this study, a mineral phase comparison between a low-release varnish comprising functionalized tricalcium phosphate (fTCP) against a high-release varnish comprising casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) was made. These calculations revealed the predominance of hydroxyapatite, fluorapatite, and calcium fluoride formation for the varnish containing fTCP, whereas the varnish containing CPP-ACP produced the same minerals along with b-TCP and octacalcium phosphate. This hypothesis shows the mineral phases expected to form from fluoride plus calcium phosphate varnishes might bear on clinical outcomes. [ABSTRACT FROM AUTHOR]

Clinically used bioceramics have been characterized previously with different kinds of methods and comparison of results have proven to be difficult due to varieties of the material properties of interest. Therefore, in this study we compared clinically commonly used bioceramics of hydroxyapatite and carbonate apatite, two bioactive glasses 45S5 and S53P4, and alumina with respect of properties which according to the present knowledge are significant for bone biology. Physicochemical properties of the materials were characterized by various methods. Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) was used to analyze the material vibrational features. X-ray Power Diffraction (XRD) was used to characterize the material crystal structure and scanning electron microscopy-energy-dispersive x-ray analysis (SEM-EDXA) was used to evaluate the morphology and size of the materials and to calculate their oxide content. The dissolution behavior of the materials, ion release and pH changes in Tris buffer in a continuous flow-through reaction for 24-hours were determined. The change of the surface of the bioactive glasses by interfacial reaction during the Tris immersion was examined and the thickness of the surface reaction layer of the materials was studied. SEM examination showed that the particle morphology of BG 45S5, BG S53P4 and alumina particle's surface was smooth. The surface of HAP was porous, but also CAP showed some surface porosity. An increase in the pH of the immersion solution was observed especially for BG 45S5 and BG S53P4. HAP, CAP and alumina caused only a minor increase in pH. BGs 45S5 and S53P4 showed a rapid initial release of sodium and calcium ions, followed by the release of silicon species. Minor release of sodium ions was registered for HAP, CAP and alumina. Calcium ion release was low but constant over the experimental time while only a minor initial dissolution was measured for HAP. The in vitro study showed differences in the materials' properties, which are considered to be important for biological suitability and in clinical applications, such as materials tomography, ion release and pH changes. [ABSTRACT FROM AUTHOR]

The aim of this study was to analyze the behavior of different bioactive glass fillers (BAGs) embedded in a polydimethylsiloxane matrix of an endodontic sealer. Three different endodontic sealers were fabricated using S53P4, 45S5 and 18−06 glass fillers. Endodontic sealer Guttaflow Bioseal consisting of polydimethylsiloxane (PDMS) matrix was used as base of the experimental sealers. Behaviors of different glass fillers leaching from polymer matrix was studied in vitro for 14 days by measuring static ion dissolution profiles of Si, Na, Ca and P -ions. In addition, pH of the simulated bodyfluid (SBF) was monitored during the 14 days and all the sealer samples was examined with SEM/EDX analysis on the surface. Identical but non-glass filler containing polydimethylsiloxane-based sealer was used as a control material. By the time point of 24 h sealer with 45S5 had released twice as much of Si-ions compared to sealer with S53P4. No statistical differences of Na, Ca and P -ions dissolution were observed in the first 168 h for any groups whereas concentrations of Ca and P -ions decreased with 45S5 significantly after 336 h. Highest pH was measured for sealers with glass filler 45S5 and S53P4 (7.64–7.65). Visible mineral precipitation was observed only on sealer surfaces after 336 h' time period with groups of 45S5 and S53P4. However, presence of calcium and phosphorus oxides was confirmed only with 45S5. Bioactive glass type 45S5 outperforms S53P4 and 18−06 by acting more dynamically in vitro set-up [ABSTRACT FROM AUTHOR]

Objective: Remineralising composites with antibacterial properties may seal the cavity and prevent secondary caries. This study aimed at developing experimental flowable composites containing different concentrations of fluoride-doped calcium phosphate fillers and evaluating their remineralising and antibacterial properties., Methods: Experimental resin-based composites containing different concentrations (0-20 %) of fluoride-doped calcium phosphate fillers (VS10/VS20) were formulated. The release of calcium (Ca), phosphate (PO) and fluoride (F) ions was assessed for 30 days. Remineralisation properties were evaluated through ATR-FTIR and SEM/EDX after storage in simulated body fluid (SBF). The metabolic activity and viability of Streptococcus gordonii was also evaluated through ATP, CFU and live/dead confocal microscopy. The evaluation of specific monomer elution from the experimental composites was conducted using high-performance liquid chromatography (HPLC)., Results: The composites containing VS10 showed the highest release of Ca, those containing VS20 released more F over time (p < 0.05), while there was no significant difference in terms of PO ions release between the groups (p > 0.05). A quick 7-day mineral precipitation was observed in the tested composites containing VS10 or VS20 at 10 %; these materials also showed the greatest antibacterial activity (p < 0.05). Moreover, the tested composites containing VS10 presented the lowest elution of monomers (p < 0.05)., Conclusions: Innovative composites were developed with low monomers elution, evident antibacterial activity against S. gordonii and important remineralisation properties due to specific ions release., Clinical Significance: Novel composites containing fluoride-doped calcium phosphates may be promising to modulate bacteria growth, promote remineralisation and reduce the risk of cytotoxicity related to monomers' elution., Competing Interests: Declaration of competing interest None of the authors have any conflict of interest with this study., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

In our previous study, we investigated the synergetic effects of inorganic ions, such as silicate, Mg2+ and Ca2+ ions on the osteoblast-like cell behaviour. Mg2+ ions play an important role in cell adhesion. In the present study, we designed a new composite that releases a high concentration of Mg2+ ions during the early stage of the bone-forming process, and silicate and Ca2+ ions continuously throughout this process. Here, 40SiO2–40MgO–20Na2O glass (G) with high solubility and vaterite-based calcium carbonate (V) were selected as the source of silicate and Mg2+ and Ca2+ ions, respectively. These particles were mixed with poly(lactic-co-glycolic acid) (PLGA) using a kneading method at 110°C to prepare the composite (G-V/PLGA, G/V/PLGA = 4/56/40 (in weight ratio)). Most of the Mg2+ ions were released within 3 days of immersion at an important stage for cell adhesion, and silicate and Ca2+ ions were released continuously at rates of 70–80 and 180 ppm d−1, respectively, throughout the experiment (until day 7). Mouse-derived osteoblast-like MC3T3-E1 proliferated more vigorously on G-V/PLGA in comparison with V-containing PLGA without G particles; it is possible to control the ion-release behaviour by incorporating a small amount of glass particles.

Objectives: This paper reviews the chemical behaviour of glass polyalkenoate (glass-ionomer) dental cements, both conventional and resin-modified, in contact with natural tissues, with the aim of determining whether these materials can be considered to be bioactive., Data: Relevant papers describing the behaviour of bioactive glasses and ceramics, and glass-ionomer (glass polyalkenoate) cements have been identified using PubMed and Science Direct. This has allowed a comparison to be made between the behaviour of glass-ionomers and the speciality glasses and ceramics that are widely classified as bioactive, a designation considered valid for over fifty years. More recent papers concerning bioactive metals and polymers have also been studied and both in vitro and in vivo studies are included., Sources: Have included general papers on the chemistry and biological behaviour of bioactive glasses and ceramics, as well as papers on glass-ionomers dealing with (i) ion release, (ii) bonding to the surface of teeth, (iii) influence on surrounding pH and (iv) interaction with bone., Conclusion: The literature shows that glass-ionomers (glass polyalkenoates) have three types of behaviour that are similar to those of bioactive glasses as follows: Formation of direct bonds to living tissue (teeth and bones) without fibrous capsule; release of biologically beneficial ions; and change of the local pH. However, in in vitro tests, they do not cause calcium phosphate to precipitate from solutions of simulated body fluid, SBF. Despite this, studies show that, in patients, glass-ionomers interact chemically with hard tissues and this suggests that may indeed be considered bioactive., Competing Interests: The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:John Nicholson reports a relationship with GC Corp that includes: consulting or advisory. The other two authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2024 The Authors. Published by Elsevier Ltd.)

Aim of the study was to evaluate apatite forming ability and ion dissolution of bioactive glass-ceramic (BGC) particles from novel polydimethylsiloxane (PDMS) based endodontic sealer Guttaflow Bioseal. Firstly, water sorption and solubility were determined for Guttaflow 2 and Guttaflow Bioseal (GB), the latter containing BGC filler particles. Mineral precipitations in simulated body fluid (SBF) were observed with SEM/EDX. Ion-release from the sealer was determined with inductively coupled plasma optical emission spectrometry (ICP-OES) in Tris-buffer solution. Change in pH was also measured. The obtained data was statistically analyzed with Tukey's HSD test (p<0.05). GB exhibited significantly higher water sorption and solubility in comparison with Guttaflow 2. Surface structure exposed particles of BGC in the PDMS matrix. The BGC particles (size of 20-40 µm) indicated to consist of CaO-SiO2-Na2O-ZrO2-P2O5. Morphologically spherical Ca/P precipitation formed after 3 days in the SBF on the sealer surface. Ca/P ratio of the precipitation ranged in 1.20-1.65 indicating transformation to hydroxyapatite (HA). The pH of the immersion solution rose gradually. [ABSTRACT FROM AUTHOR]

Different surface treatments are applied to improve the surface properties of metallic biomaterials. Chemical etching is one of the common techniques used for roughening the surface. In this regard, the effects of different chemical media on the surface roughness, degradation, and ion release of 316L SS steel were investigated in this study. The 316L SS steel was exposed to chemical etching in six different chemical media including HNO 3 , H 2 SO 4 , HCl, HClO 4 , NaOH and Na 2 CO, at four different concentrations (1, 2, 4, and 8 Molar), and at three immersion times (10, 60, and 180 min). SEM, EDS, and XRD analyses were used to examine the morphological and chemical impacts of chemical etching on sample surfaces, and roughness was measured on all sample surfaces. The effect of surface treatment on the degradation and ion release of the samples was comparatively examined. Characterization analyses indicated that the HNO 3 , H 2 SO 4 , and HCl media did not cause a significant reaction on the surface of the 316L SS. On the other hand, different phases were observed on the sample surfaces exposed to HClO 4 , NaOH, and Na 2 CO 3 media. It was determined that the roughness had no linear correlation with the concentration and immersion time, and similarly, the degree of degradation and amount of ion release displayed no change depending on the roughness. Samples etched in H 2 SO 4 , HClO 4 , NaOH and Na 2 CO 3 provided the highest roughness. It was found that H 2 SO 4 caused a significant increase in the amount of ion release. • Six different chemical etching media were applied to etch 316L SS. • No significant reaction was observed in the media of H 2 O, HNO 3 , H 2 SO 4 , and HCl. • Different phases from austenite were detected in HClO 4 , NaOH and Na 2 CO 3. • Samples etched in H 2 SO 4 , HClO 4 , NaOH and Na 2 CO 3 provided the highest roughness. • It was found that H 2 SO 4 caused a significant increase in the amount of ion release. [ABSTRACT FROM AUTHOR]

Abstract: Objectives: This study was undertaken to gain a fuller picture of the interaction of resin-modified glass-ionomers with aqueous solutions in terms of water sorption, solution buffering and ion-release. Methods: Two commercial materials were employed (Fuji II LC, GC; Photac Fil Quick, 3M ESPE). Light-cured cylindrical specimens (6mm high×4mm diameter) were prepared and stored for up to 6 weeks in either water (pH 5.3) or aqueous lactic acid (2.7), six specimens of each materials per storage medium. Solutions were changed at weekly intervals. Specimens were weighed at weeks 1, 2, 4 and 6; solution pH values measured, and Na, Ca, Sr, Al, P and Si ion release determined using ICP-OES. Results were analysed by ANOVA. Results: Materials altered solution pH, and gained mass under all conditions. However, the net mass gain in lactic acid declined with time, suggesting that water sorption was partly offset by erosion under acid conditions. Na, Ca, Sr, Al, P and Si were detected in all solutions, with greater amounts in lactic acid than in water. Phosphorus release was much lower than found previously for conventional glass-ionomers. Significance: Like their conventional counterparts, resin-modified glass-ionomers have been found to buffer their storage media and release ions. Hence the resin phase does not significantly alter these aspects of the interaction with aqueous solutions. [Copyright &y& Elsevier]

Specimens of an experimental glass-ionomer cement were stored in water (initial pH 5.9) and aqueous lactic acid (initial pH 2.7) for storage periods of 1 week up to 6 weeks. Change in mass, solution pH and fluoride release were measured at weekly intervals, and other ions were determined at weeks 1, 2, 4 and 6. In water, cements raised the pH consistently to 6.7–6.9 from weeks 2 to 6, but this did not correspond to uniform amounts of ions released, nor even to consistent mole ratios of ions in solution. Similarly, in lactic acid, pH was raised to between 3.6 and 4.5, but without a consistent concentration of ions in solution. In near neutral conditions, calcium was found to be virtually insoluble and remained within the cement, whereas reasonable amounts of sodium, aluminium, phosphorus, silicon and fluoride were released at all time intervals, with downward trends over time. In acidic conditions, considerable amounts of calcium were released over time, and amounts of calcium, aluminium, phosphorus and silicon increased with time, reaching a maximum in week 4. This suggests that as maturation proceeds, there is an increase in the acid-soluble fraction of the cement containing these elements. Fluoride release was found to be as previously reported, i.e. greater amounts in the early stages of the experiment, and with a gradual decline, and with greater amounts in acid than in water. Determination of fluoride with and without the decomplexing reagent TISAB showed that 70–75% of the total fluoride was released in “free” form in water for most weeks, whereas in acid, it declined sharply and by week 6, an estimated total of 96% of the fluoride released was complexed. [Copyright &y& Elsevier]

In our previous study, we investigated the synergetic effects of inorganic ions, such as silicate, Mg 2+ and Ca 2+ ions on the osteoblast-like cell behaviour. Mg 2+ ions play an important role in cell adhesion. In the present study, we designed a new composite that releases a high concentration of Mg 2+ ions during the early stage of the bone-forming process, and silicate and Ca 2+ ions continuously throughout this process. Here, 40SiO 2 -40MgO-20Na 2 O glass (G) with high solubility and vaterite-based calcium carbonate (V) were selected as the source of silicate and Mg 2+ and Ca 2+ ions, respectively. These particles were mixed with poly(lactic- co -glycolic acid) (PLGA) using a kneading method at 110°C to prepare the composite (G-V/PLGA, G/V/PLGA = 4/56/40 (in weight ratio)). Most of the Mg 2+ ions were released within 3 days of immersion at an important stage for cell adhesion, and silicate and Ca 2+ ions were released continuously at rates of 70-80 and 180 ppm d -1 , respectively, throughout the experiment (until day 7). Mouse-derived osteoblast-like MC3T3-E1 proliferated more vigorously on G-V/PLGA in comparison with V-containing PLGA without G particles; it is possible to control the ion-release behaviour by incorporating a small amount of glass particles., Competing Interests: The authors declare we have no competing interests., (© 2019 The Authors.)