scholarly journals The Evaluation of Formation and Bioactivity of New Sol-gel Bioactive Glass

Author(s):  
Bui Xuan Vuong

In this paper, three ceramic compositions 50SiO2-50CaO (A), 45SiO2-45CaO-10P2O5 (B) and 40SiO2-40CaO-20P2O5 (C) (wt %) were synthesized by using the sol-gel technique. XRD analysis demonstrates that only sample C can form the glass material. Treated temperatures and heated times were also evaluated. Analysis data showed that the bioglass 40SiO2-40CaO-20P2O5 (wt %) can successfully elaborate when the ceramic powder heated at 750 oC for 3 hours. ‘‘In vitro’’ experiment was effectuated to investigate the bioactivity of bioglass 40SiO2-40CaO-20P2O5 by soaking powder samples in SBF solution. Obtained result confirmed the formation of hydroxyapatite (HA) phase on glass’s surface after 15 days of immersion, in which HA formation orients following (211) and (222) miller planes in crystalline structure of HA phase. Keywords Sol-gel; bioglass; hydroxyapatite; SBF; bioactivity References [1] D.F. Williams, Definitions in Biomaterials, Consensus Conference for the European Society for Biomaterials, Chester, UK, 1986.[2] L.L. Hench, Bioceramics: From Concept to Clinic, Journal of the American Ceramic Society, 74 (1991) 1487.[3] L.L. Hench, The story of Bioglass, Journal of Materials Science: Materials in Medicine, 17 (2006) 967.[4] X.V. Bui, H. Oudadesse, Y. Le Gal, A. Mostafa, P.Pellen and G. Cathelineau, Chemical Reactivity of Biocomposite Glass-Zoledronate, Journal of the Australian Ceramic Society, 46 (2010) 24.[5] L.L. Hench, Genetic design of bioactive glass, Journal of the European Ceramic Society, 29 (2009) 1257.[6] S. Kumar, P. Vinatier, A. Levasseur, K.J. Rao, Investigations of structure and transport in lithium and silver borophosphate glasses, Journal of Solid State Chemistry, 177 (2004)1723.[7] Z. Hong, A. Liu, L. Chen, X. Chen, X. Jing, Preparation of bioactive glass ceramic nanoparticles by combination of sol–gel and coprecipitation method, Journal of Non-Crystalline Solids, 355 (2009) 368.[8] D.B. Joroch, D.C. Clupper, Modulation of zinc release from bioactive sol–gel derived SiO2‐CaO‐ZnO glasses and ceramics, Journal of Biomedical Materials Research Part A, 82A (2007) 575.[9] J. Roman, S. Padilla, M. Vallet-Regi, Sol−Gel Glasses as Precursors of Bioactive Glass Ceramics, Chemistry of Materials, 15 (2003) 798.[10] J. Lao, J.M. Nedelec, Ph. Moretto, E. Jallot, Biological activity of a SiO2-CaO-P2O5 sol-gel glass highlighted by PIXE-RBS methods, Nuclear Instruments and Methods in Physics Research Section B, 245 (2006) 511.[11] [11] M. Vallet-Regi, L. Ruiz-Gonzalez, I. Izquierdo, J.M. Gonzalez-Calbet, Revisiting silica based ordered mesoporous materials: medical applications, Journal of Materials Chemistry, 16 (2006) 26.[12] W. Xia, J. Chang, Preparation and characterization of nano-bioactive-glasses (NBG) by a quick alkali-mediated sol–gel method, Materials Letters 61 (2007) 3251.[13] R. Li, A.E. Clark, L.L. Hench, An investigation of Bioactive Glass Powders by Sol-Gel Processing, Transactions of 16th Annual Meeting of the Societey for Biomaterials, 12 (1990) 40.[14] J. Lao, J.M. Nedelec, P. Moretto, E. Jallot, Imaging physicochemical reactions occurring at the pore surface in binary bioactive glass foams by micro ion beam analysis, Applied Materials and Interfaces, 6 (2010) 1737.[15] A. Balamurugan, G. Balossier, S. Kannan, J. Michel, A.H.S. Rebelo, J.M.F. Ferreira, Development and in vitro characterization of sol–gel derived CaO–P2O5–SiO2–ZnO bioglas, Acta Biomaterialia, 3 (2007) 255.[16] Z. Hong, A. Liu, L. Chen, X. Chen, X. Jing, Bioactive glass prepared by sol–gel emulsion, Journal of Non-Crystalline Solids, 355 (2009) 368.[17] O. Peital, E.D. Zanotto, L.L. Hench, Highly bioactive P2O5-Na2O-CaO-SiO2 glass-ceramics, Journal of Non-Crystalline Solids, 292 (2001) 115.[18] J. Liu, X. Miao, Sol-gel derived bioglass as a coating material for porous alumina scaffolds, Ceramics International, 30 (2004) 1781.[19] T. Kokubo, H. Takadama, How useful is SBF in predicting in vivo bone bioactivity. Biomaterials 27 (2006) 2907.[20] M. Dziadek, B. Zagrajczuk, P. Jelen, Z. Olejniczak, K.C. Kowalska, Structural variations of bioactive glasses obtained by different synthesis routes, Ceramics International, 42 (2016) 14700.[21] R. Lakshmi, V. Velmurugan and S. Sasikumar, Preparation and Phase Evolution of Wollastonite by Sol-Gel Combustion Method Using Sucrose as the Fuel, Combustion Science and Technology, 185 (2013) 1777.[22] G. Voicu, A. Bădănoiu, E. Andronescu1, C. M. Chifiruc, Synthesis, characterization and bioevaluation of partially stabilized cements for medical applications, Central European Journal of Chemistry, 11 (2013) 1657.[23] M.V. Regi, Ceramics for medical applications, Journal of the Chemical Society, Dalton Transactions, 2 (2001) 97.[24] G. Voicu, A.I. Bădănoiu, E. Andronescu, C.M. Chifiruc, Synthesis, characterization and bioevaluation of partially stabilized cements for medical applications, Central European Journal of Chemistry, 11 (2013) 1657.M. Wu, T. Wang, Y. Wang, F. Li, M. Zhou, X. Wu, A novel and facile route for synthesis of fine tricalcium silicate powders, Materials letters, 227 (2018), 187.

2008 ◽  
Vol 396-398 ◽  
pp. 131-134 ◽  
Author(s):  
Ourania Menti Goudouri ◽  
Xanthippi Chatzistavrou ◽  
Eleana Kontonasaki ◽  
Nikolaos Kantiranis ◽  
Lambrini Papadopoulou ◽  
...  

Thermal treatment of bioactive glasses can affect their microstructure and thus their bioactivity. The aim of this study was the characterization of the thermally treated sol-gel-derived bioactive glass 58S at characteristic temperatures and the dependence of its bioactive behavior on the specific thermal treatment. The thermal behavior of the bioactive glass was studied by thermal analysis (TG/DTA). Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffractometry (XRD) were used for the characterization of the bioactive glass. The bioactive behavior in Simulated Body Fluid (SBF) was examined by Scanning Electron Microscopy (SEM-EDS) and FTIR. The major crystal phases after thermal treatment were Calcium Silicates, Wollastonite and Pseudowollastonite, while all thermally treated samples developed apatite after 48 hours in SBF. A slight enhancement of bioactivity was observed for the samples heated at the temperature range 910-970oC.


2011 ◽  
Vol 493-494 ◽  
pp. 85-89 ◽  
Author(s):  
Viorica Simon ◽  
R. Ciceo Lucacel ◽  
I. Titorencu ◽  
V. Jinga

Lime phosphosilicate and soda lime phosphosilicate glasses prepared by sol-gel method were precursors of bioactive glass-ceramics. The structure of the samples and the distribution of the [SiO4] units was investigated by X-ray diffraction and infrared spectroscopy. Human osteosarcoma cell line (MG63) was used for the in vitro cellular response. DNA staining (Hoechst 33258) assay was performed for assessing samples colonization.


2020 ◽  
Author(s):  
Reedwan Bin Zafar Auniq ◽  
Namon Hirun ◽  
Upsorn Boonyang

Bioactive glass ceramics (BGCs) have been used in orthopedic and dentistry due to having better osteoconductive and osteostimulative properties. This study aimed to evaluate and compare the drug release properties of two different BGCs; 45S5 and S53P4. The BGCs were composed with four phases of SiO2 – CaO – Na2O – P2O5 system, synthesized by sol–gel method using dual templates; a block-copolymer as mesoporous templates and polymer colloidal crystals as macroporous templates, called three-dimensionally ordered macroporous-mesoporous bioactive glass ceramics (3DOM-MBGCs). In vitro bioactivity test performed by soaking the 3DOM-MBGCs in simulated body fluid (SBF) at 37°C. The results indicated that, the 45S5 have the ability to grow hydroxyapatite-like layer on the surfaces faster than S53P4. Gentamicin drug was used to examine in vitro drug release properties in phosphate buffer solution (PBS). The amount of drug release was quantified through UV/Vis spectroscopy by using o-phthaldialdehyde reagent. S53P4 showed high drug loading content. The outcome of drug release in PBS showed that both S53P4 and 45S5 exhibited a slowly continuous gentamicin release. The resultant drug release profiles were fitted to the Peppas-Korsmeyer model to establish the predominant drug release mechanisms, which revealed that the kinetics of drug release from the glasses mostly dominated by Fickian diffusion mechanism.


2013 ◽  
Vol 19 (2) ◽  
pp. 231-239 ◽  
Author(s):  
Nima Nabian ◽  
Maedeh Delavar ◽  
Mahmood Rabiee ◽  
Mohsen Jahanshahi

The paper reports the first attempt at changing cooling treatment of synthesizing method in order to investigate its effect on the physical properties of sol-gel derived nano bioactive glass-ceramic in the system 58SiO2-33CaO-9P2O5 (wt.%). We hypothesized that the method of cooling may affect the properties of nano bioactive glass-ceramic. To test this hypothesis, two different method of cooling treatment was applied after calcinations in synthesizing method. Both quenched and unquenched nano bioactive glass-ceramics were soaked in Ringer?s solution with bovine serum albumin (BSA) for bioactivity evaluation. The obtained samples were analyzed for their composition, crystalinity and morphology through X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), surface electron microscope (SEM) and transmission electron microscope (TEM). The SEM images showed that the morphology of nano bioactive glass-ceramics was completely changed by quenching process. Results of in vitro bioactivity evaluation revealed that the unquenched attains faster apatite formation ability than the quenched sample. Other properties of these two morphologically different nano bioactive glass-ceramics were strongly discussed.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Shirong Ni ◽  
Ruilin Du ◽  
Siyu Ni

The aim of this study was to investigate the effect of Na and Ti on thein vitrodegradation and bioactivity in the 58S bioactive glass. The degradation was evaluated through the activation energy of Si ion release from bioactive glasses and the weight loss of bioactive glasses in Tris-HCl buffer solution. Thein vitrobioactivity of the bioactive glasses was investigated by analysis of apatite-formation ability in the simulated body fluid (SBF). The results showed that Na in the 58S glass accelerated the dissolution rate of the glass, whereas Ti in the 58S glass slowed down the rate of glass solubility. Bioactivity tests showed that Na in glass increased the apatite-forming ability in SBF. In contrast, Ti in glass retards the apatite formation at the initial stage of SBF soaking but does not affect the growth of apatite after long periods of soaking.


2006 ◽  
Vol 49 ◽  
pp. 103-108
Author(s):  
R. Sindut ◽  
Katarzyna Cholewa-Kowalska ◽  
Maria Łączka

Bioglasses and bioactive glass-ceramics have found increasingly wide application in medicine and dentistry. Using sol-gel method, is possible to obtain glass and glass-ceramic bioactive materials of new generation, characterized the higher bioactivity than melted bioglasses. These materials can be produced in various final forms, as powders, thin layers on different base and porous sinters. Production of porous bioactive sinters from gel-derived powders is a new problem and the parameters controlling this process are not recognized yet. The aim of the study was to obtain porous bioactive sinters from gel-derived powders of the SiO2-CaO-P2O5 system of four various chemical compositions (S2, II, I, A2) and the characterization of properties of these new materials. The starting powders differ from each other in the content of the basic components, at the molar ratio of CaO to SiO2 equals 0.2-1.35. To obtain the porous sinters a method of burning additions and deposition of the casting slip on the polymeric sponge was used. Sintering was realized in several stages, at the maximal temperature 1200oC. By selecting appropriate conditions of sintering, a durable material of high open porosity up to 77 % was obtained. Its porous structure was characterized by a prevailing number of small micropores of similar dimensions, uniformly distributed in the material. The phase composition of obtained sinters was determined by the X-ray diffraction method. All sinters represented glass-ceramic materials with apatite, cristoballite and calcium silicates as a main crystalline phases. In order to preliminary determination bioactivity of obtained sinters, test in vitro in simulated body fluid SBF was conducted. It was found that hydroxyapatite formation on the sinter surface occurs only in the case of biomaterials of highest calcium concentration.


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