scholarly journals Synthesis of borate modified bioactive glass scaffold using PVP burning-out method for bone tissue replacement

2019 ◽  
Vol 9 (4) ◽  
pp. 4044-4049 ◽  

Three-dimensional (3D) bioactive glass scaffolds are one of the most studied types of scaffolds for bone tissue replacement because of their excellent bioactivity and potential for stimulating osteogenesis and angiogenesis. In the present study, modified Hench- based bioglass was fabricated by polyvinyl pyrrolidone (PVP) burning-out method for producing porous scaffold. In vitro investigation of the scaffolds’ bioactivity was achieved through examining changes in its composition during exposing to physiological simulated body fluid (SBF) solution via Fourier transform-infrared (FT-IR) absorption spectroscopy, X-ray diffraction (XRD) analysis, Scanning electron microscopy (SEM) supported by Energy-dispersive X-ray (EDX). FT-IR spectral data was used to validate the formation of hydroxyapatite as an indication of the bioactivity potential of the studied scaffold post incubation in SBF. The prepared samples were examined by XRD to recognize the crystalline phase/phases that may formed after immersion in physiological solutions and supported via (SEM/EDX) data.

Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.


2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.


2015 ◽  
Vol 1 (1) ◽  
Author(s):  
M. Araújo ◽  
M. Miola ◽  
A. Venturello ◽  
G. Baldi ◽  
J. Perez ◽  
...  

AbstractIn this work, sintered pellets of a silica-based bioactive glass were dip-coated with a biocompatible natural-derived polymer in order to investigate the influence of the organic coating on the glass bioactivity. After the sintering process optimization, uncoated and coated pellets have been characterized by means of scanning electron microscopy with energy dispersive spectroscopy (SEM, EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and pH measurements, after the immersion in a simulated body fluid (SBF). An increased apatite forming ability and a better control of the pH during soaking of the samples in SBF were observed in the presence of the biopolymer. This result opens a new insight on the simple fabrication of highly bioactive hybrid inorganic-organic materials for medical applications.


2015 ◽  
Vol 638 ◽  
pp. 67-72
Author(s):  
Ana Maria Salantiu ◽  
Florin Popa ◽  
Petru Pascuta ◽  
Olga Soritau ◽  
Noemi Dirzu ◽  
...  

This work aims to investigate the influence of surface conditioning of porous Ti for enhancing its biological activity, as assessed by in vitro stem cell testing. Porous Ti samples with an average porosity of 32% were processed by Powder Metallurgy with dextrin as a space holder. The samples were subjected to H2O2 treatment to form an enhanced TiO2 film, followed by a heat treatment at 400°C and 600°C aiming to the crystallization of the as-formed amorphous titanium oxide. Samples characterization was performed by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR) and X-Ray Diffraction (XRD). The treated surfaces revealed to be made of both anatase and rutile TiO2, with groove–shaped structure and cracks on the surface of the TiO2 film. The intrinsic biocompatibility of the chemically modified porous Ti surfaces was assessed in vitro. In our cell culture tests, stem cells were found to attach and proliferate better on the chemically treated Ti surfaces compared to the control untreated Ti surfaces.


2021 ◽  
pp. 889-896
Author(s):  
Hanan J. Mustafa ◽  
Tagreed M. Al-Saadi

To study the removal of lead (Pb) ions from aqueous solutions, novel magnetite nanoparticles (NPs) of Ni0.31Mg0.15Ag0.04Fe2.5O4 were synthesized by coprecipitation synthesis using metal sulfates, and then coated with Gum Arabic (GA). The prepared NPs were analyzed using various spectroscopic and analytical methods, such as X-Ray diffraction analysis (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray spectroscopy (EDX), Fourier Transform Infra-Red spectroscopy (FT-IR), and Atomic Absorption Spectrophotometer (AAS). By using XRD analysis, the cubic inverse spinel structure of the prepared NPs was proven, showing average values of crystallite size, lattice constant, and density of 28.57nm, 8.32582Å, and 5.2890 g/cm3, respectively. FE-SEM analysis revealed the sphere-like shape of the nanoparticles with a measured crystallite size of 25.93nm. The existence of constituent elements was evidenced by EDX. FT-IR test proved the success of the coating process of magnetite NPs by the presence of the main characteristic absorption bands of GA in the FT-IR spectrum of GA-magnetite NPs. The adsorption of Pb ions by GA- magnetite NPs was shown by AAS analysis, where the concentration of Pb ions decreased from 25ppm to 6.6ppm, reaching 1.1ppm at the time of 25min. The porosity of the NPs and the carboxyl groups in GA played an important role in the process.


2019 ◽  
Vol 41 (6) ◽  
pp. 1090-1090
Author(s):  
Mehmet Poyraz Mehmet Poyraz ◽  
Musa Sari Musa Sari ◽  
Halil Berber Halil Berber ◽  
Nursenem Karaca and Fatih Demirci Nursenem Karaca and Fatih Demirci

A new Schiff base, namely 2-methoxy-6-((2-(4 nitrophenyl) hydrazineylidene) methyl)phenol was synthesized and characterized by melting points, elemental analysis, thermogravimetric analysis and spectroscopic techniques (FT-IR, 1H-NMR and UV-VIS spectra). The chemical structure of compound was further confirmed by single crystal structural X-ray diffraction. The Schiff base is crystallized in the triclinic space group P-1. In the crystal, molecules are linked by O-H…O hydrogen bonds between the hydroxy “-O-” atom and the methoxy “-O-” atom. Furthermore, the synthesized Schiff base was tested for the in vitro anticandidal activities using CLSI broth microdilution method against human pathogenic Candida albicans, C. parapsilosis and C. krusei standard strains. In the anticandidal activity test results, the new Schiff base was found to be effective at 1 mg/mL - 0.25 mg/mL concentrations. (The last line omitted) (The sentence marked in red will be deleted)


2014 ◽  
Vol 96 ◽  
pp. 21-26 ◽  
Author(s):  
P.J. Reséndiz-Hernández ◽  
D.A. Cortés-Hernández ◽  
Juan Méndez Nonell ◽  
J.C. Escobedo-Bocardo

Silica aerogels have attracted increasingly more attention due to their extraordinary properties and their existing and potential applications in a wide variety of technological areas. Materials that promote bone-tissue formation at their surface and bond to osseous tissues when implanted are called bioactive, such as pseudowollastonite particles. In this work, the synthesis of aerogels with pseudowollastonite particles was performed. The synthesis involved the preparation of an alcogel by a two step sol-gel route followed by ambient pressure drying. To promote a higher bioactivity the obtained aerogels were then biomimetically treated using simulated body fluids, SBF and 1.5 SBF. A high bioactivity was demonstrated by FT-IR, SEM, EDS, and XRD. The in vitro biocompatibility was assessed by testing cytotoxicity using rat osteoblasts cultures. The results obtained indicate that these materials are highly potential aerogels for bone tissue regeneration.


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