scholarly journals In vitro bioactivity of glass-ceramic/fibroin composites

2017 ◽  
Vol 11 (2) ◽  
pp. 136-146 ◽  
Author(s):  
Lachezar Radev ◽  
Irena Michailova ◽  
Silviya Stateva ◽  
Diana Zaimova ◽  
Hristo Georgiev ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
In Vitro Tests ◽  
In Vitro Bioactivity ◽  
X Ray ◽  
Before And After ◽  
Static Conditions

Bioactive composite materials were prepared by mixing 20 wt.% of silk fibroin (SF) and 80 wt.% of glassceramics from CaO-SiO2-P2O5-MgO system. In vitro bioactivity of the prepared composites was evaluated in 1.5 simulated body fluid (1.5 SBF) in static conditions. The obtained samples before and after in vitro tests were characterized by X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The changes in 1.5 SBF solutions after soaking the samples were evaluated by inductively coupled plasma atomic emission spectroscopy (ICP-AES). MG63 osteosarcoma cells were used for the biological experiments. The obtained experimental data proved that the synthesized composites exhibit excellent in vitro bioactivity.

scholarly journals Collagen/silicocarnotite composites, cross-linked with chondroitin sulphate: In vitro bioactivity

2011 ◽  
Vol 5 (3) ◽  
pp. 161-170 ◽  
Author(s):  
Lachezar Radev ◽  
Vladimir Hristov ◽  
Irena Michailova ◽  
Maria Fernandes ◽  
Isabel Salvado
Keyword(s):  
Inductively Coupled Plasma ◽  
Chondroitin Sulphate ◽  
Atomic Emission ◽  
Red Shift ◽  
Structure Evolution ◽  
In Vitro Test ◽  
In Vitro Bioactivity ◽  
Before And After ◽  
Vitro Test

In this work we present the experimental results on synthesis, structure evolution and in vitro bioactivity of collagen- silicocarnotite-chondroitin sulphate composites. The obtained samples were synthesised by mixing collagen (C) and silicocarnotite (S) powder with C:S ratio of 75:25 and 25:75 wt.% in the presence of chondroitin sulphate (ChS). Collagen was diluted in 5M CH3COOH before mixing. The obtained materials were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) before and after in vitro test in 1.5 simulated body fluid. XRD of synthesized samples showed that before immersion carbonate containing hydroxyapatite (CO3HA) were formed in situ in the composites. FTIR depicts the presence of HPO4 2- and the 'red shift' of COO- and SO3 - from ChS was also observed. This 'red shift' could be attributed that the ChS prefers to chelate Ca2+ from partially dissolved S powder. SEM of the prepared samples show the presence of nanosized hydroxyapatite (HA) whiskers and flower-like HA assemblies. After in vitro test, XRD proved the presence of HA with well-defined crystallinity. According to the FTIR results B-type CO3HA can be observed. SEM of the precipitated layers show the presence of HA spheres. Inductively coupled plasma atomic emission spectroscopy results lead to a conclusion that after in vitro test of the prepared composites silicon containing carbonate substituted hydroxyapatite (Si-CO3HA) may be formed on the surface of the immersed samples.

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

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.

scholarly journals In vitro bioactivity of Polyurethane/85S Bioglass composite scaffolds

2013 ◽  
Vol 11 (9) ◽  
pp. 1439-1446 ◽  
Author(s):  
Lachezar Radev ◽  
Darina Zheleva ◽  
Irena Michailova
Keyword(s):  
Sol Gel ◽  
Spherical Particles ◽  
Polymerization Reaction ◽  
In Vitro Test ◽  
In Vitro Bioactivity ◽  
Before And After ◽  
Vitro Test ◽  
Sbf Solution ◽  
Static Conditions

AbstractIn the present work Polyurethane (PU)/Bioglass (BG) composite materials were synthesized with different content of BG (10 and 20 mol.%) as filler. The 85S Bioglass was synthesized via polystep sol-gel method. The chemical composition of BG is 85SiO2-10CaO-5P2O5 (wt.%). The synthesis of PU was carried out by a two-step polyaddition reaction. The 85S BG was added in situ during the polymerization reaction. In vitro bioactivity of the prepared composites was examined in the presence of 1.5 SBF for 7 days in static conditions. The structure of synthesized PU/BG composites before and after in vitro test was determined by XRD, FTIR and SEM. XRD of the samples before in vitro test proved that the phase of γCa2P2O7 in the PU/20BG is visible. FTIR revealed the presence of urethane bond between OH-(from BG) and NCO groups (from PU). Based on FTIR results after in vitro test in 1.5 SBF solutions, A/B-carbonate containing hydroxyapatite (CO3HA) was formed. XRD proved that HA was formed on the surface of the samples, but Ca2P2O7 does not undergo any changes in the 1.5 SBF solution. SEM depicted the nano-HA agglomerated in spherical particles after immersion in 1.5 SBF for 7 days.

scholarly journals In vitro Antimicrobial Effects of Virus Block, Which Contains Multiple Polyoxometalate Compounds, and Hygienic Effects of Virus Block-Supplemented Moist Hand Towels

Pharmacology ◽  
2019 ◽  
Vol 104 (1-2) ◽  
pp. 98-112 ◽  
Author(s):  
Katsuaki Dan ◽  
Naohiro Katoh ◽  
Takaaki Matsuoka ◽  
Katsuyuki Fujinami
Keyword(s):  
Inductively Coupled Plasma ◽  
Metal Ion ◽  
Bacterial Flora ◽  
Atomic Emission ◽  
Time Dependent ◽  
Antimicrobial Effects ◽  
Inductively Coupled ◽  
Before And After ◽  
Normal Bacterial Flora

Background: Historical evidence has verified the multifaceted antiviral efficacy of polyoxometalates (PMs). Methods: We carried out a study to investigate the antimicrobial effects of each of the 5 substances comprising virus block (VB): 3 PMs that have antibacterial and antiviral activity, an antibiotic agent, and an antibacterial agent. We also investigated the effectiveness of the addition of VB to moist hand towels in a study involving 120 volunteers. The time-dependent changes in metal ion concentrations in aqueous VB solution were analyzed using inductively coupled plasma atomic emission spectroscopy. Results: The metal elements in the aqueous VB solution remained stable for 12 weeks without undergoing time-dependent changes. Discussion: Further investigations were performed to study hand hygiene using moist hand towels in daily life settings. To this end, 120 volunteers provided 240 specimens that were used to investigate the presence of antibacterial compounds on the volunteers’ hands before and after hand towel use. An aliquot of each specimen was suspended in phosphate-buffered saline and plated on agar media, and the number of colonies formed was counted. Normal bacterial flora found on the hands of the volunteers was investigated before and after the use of 4 different moist hand towels. Conclusions: The effects of VB and PMs were superior to those of commercial moist hand towels, indicating that effective data were obtained that may be useful for the practical application of the tested items.

Photocatalytic Oxidation of Alcohols Over Magnetically Recoverable Gold Supported Iron Oxide Nanoparticles

2019 ◽  
Vol 11 (12) ◽  
pp. 1731-1738 ◽  
Author(s):  
Ma Hui ◽  
Wu Juzhen ◽  
Zhao Li ◽  
Zhou Zheng ◽  
Guo Jiahu
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Photocatalytic Oxidation ◽  
Organic Dyes ◽  
Atomic Emission ◽  
One Pot ◽  
X Ray ◽  
Inductively Coupled ◽  
Oxidation Of Alcohols

A one-pot simple and efficient synthetic route for the synthesis of Au-loaded Fe2O3 nanoparticles was developed, and this material's photocatalytic activity for visible light assisted oxidation of alcohols and degradation of organic dye were studied. As-synthesized nanostructured catalyst was characterised by powder X-ray diffraction (XRD), transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), SEM-mapping, X-ray photoelectron spectroscopy (XPS), N2 adsorption–desorption isotherm (BET), and inductively coupled plasma-atomic emission spectroscopy (ICP-AES). It was observed that 5–10 nm Au-nanoparticles supported on 10–80 nm Fe2O3 shows boomerang-shaped nanoparticle. Gold loading of 1 wt% shows high conversion and selectivity towards the target product aldehyde. The synthesized nanomaterial also proved to be an excellent photocatalyst for degradation of organic dyes such as methylene blue (MB) and rhodamine B (RhB). The catalyst proved to be noteworthy as it does not loss in its catalytic activity even after five cycles of reuse.

Growth of Calcium Phosphate on Poled Piezoelectric Poly-L-lactic Acid Membrane by a Biomimetic Method

2007 ◽  
Vol 330-332 ◽  
pp. 703-706
Author(s):  
Chun Peng Huang ◽  
Dong Hua Guan ◽  
Kun Tian ◽  
Xin Min Chen ◽  
Lin Niu ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Electric Field ◽  
Photoelectron Spectroscopy ◽  
Charged Surface ◽  
X Ray ◽  
Charged Surfaces ◽  
Before And After ◽  
Dc Electric Field ◽  
Biomimetic Method

The bioactivity of poled piezoelectric PLLA membrane was investigated by studying the calcium phosphate formation in vitro using a biomimetic method. Samples (φ10mm) were poled under DC electric field of 8~l0kV/cm at 70°C for 30 min followed by cooling under the electric field. Surface chemistry of the samples before and after poling treatment was studied by X-ray photoelectron spectroscopy (XPS). Poled/unpoled samples were immersed in supersaturated calcification solution (SCS) for periods up to 24 h (36.5°C). The surface morphology and composition of the soaked samples were evaluated by using scanning electron microscope (SEM) and X-ray diffraction analysis (XRD). Poled samples showed two different charged surfaces, negatively-charged surface (N-PLLA) and positively-charged surface (P-PLLA). On the N-PLLA surfaces, SEM together with XRD showed a gradually formed calcium phosphate (Ca-P), while no obvious Ca-P on either P-PLLA or unpoled samples was observed. This study demonstrated that poled piezoelectric PLLA substrates induce substantially higher level of Ca-P formation than electrically neutral substrates and only N-PLLA, however, can improve Ca-P formation after immersion in SCS.

Antiphotocorrosive photocatalysts containing CdS nanoparticles and exfoliated TiO2 nanosheets

2010 ◽  
Vol 25 (1) ◽  
pp. 182-188 ◽  
Author(s):  
Xiaoxia Yan ◽  
Gang Liu ◽  
Lianzhou Wang ◽  
Yong Wang ◽  
Xianfang Zhu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Cds Nanoparticles ◽  
Visible Absorption ◽  
X Ray ◽  
Tio2 Nanosheets

Aimed at designing an efficient visible light active photocatalyst and suppressing the self-corrosion tendency of CdS nanoparticles, a novel composite consisting of CdS nanoparticles and exfoliated two-dimensional (2D) TiO2 nanosheets was successfully fabricated using a simple self-assembly process. The prepared samples were characterized using various techniques including x-ray diffraction, ultraviolet–visible absorption spectroscopy, x-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. It was found that the exfoliated 2D nanosheets played an important role as an ultrathin coating to suppress the photocorrosion of CdS nanoparticles, evidenced by inductively coupled plasma-atomic emission spectrometer analysis. The resultant CdS/TiO2 composites exhibited enhanced photocatalytic activity in the oxidation of Rhodamine B in water under visible light irradiation (λ > 420 nm).

scholarly journals A sol-gel synthesis, characterization and in vitro bioactivity of binary, ternary and quaternary bioglasses with high mechanical strength

2020 ◽  
Vol 10 (4) ◽  
pp. 310-318
Author(s):  
Sara Bouhazma ◽  
Imane Adouar ◽  
Sanae Chajri ◽  
Smaiel Herradi ◽  
Mohamed Khaldi ◽  
...  
Keyword(s):  
Sol Gel ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
In Vitro Tests ◽  
In Vitro Bioactivity ◽  
X Ray Diffraction ◽  
High Mechanical Strength ◽  
X Ray ◽  
Sol Gel Synthesis

Bioactive powders of the binary SiO2-CaO, ternary SiO2-CaO-P2O5 and quaternary systems SiO2-CaO-P2O5-Na2O/Mg2O were synthesized using a sol-gel route. The gels were converted into bioglasses powders by heat treatments at the temperature of 700°C. The resulting materials were characterized by X-ray diffraction (XRD), Fourier Transform Infrared spectroscopy (FTIR), Environmental Scanning Electron Microscopy (ESEM) and in vitro bioactivity in acellular Simulated Body Fluid (SBF). The in vitro tests showed that the samples had good apatite-forming ability. Glasses doped with sodium and magnesium show good results in terms of bioactivity and mechanical properties. The results showed that the quaternary glass SiO2-CaO-P2O5-Na2O containing Na is the most bioactive, only 6 hours after its immersion in SBF; a layer of hydroxycarbonated apatite (HAC) was deposited on the glass and compressive strength of up to 233.08 MPa with a porosity of 11.02%, due to the presence of the Na2Ca2Si3O9 phase. Magnesium also affects bioactivity because it has improved from binary to ternary to quaternary doped with magnesium, bioactive from 12h of contact with the SBF.

scholarly journals The Modification of Pt/Graphene Composites with Oxophilic Metal Bi (Bi2O3) and Its Dual-Functional Electro-Photo Catalytic Performance

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 465
Author(s):  
Yingli Wu ◽  
Xiuyun Duan ◽  
Zhongshui Li ◽  
Shuhong Xu ◽  
Yixin Xie ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Electric Energy ◽  
Atomic Emission ◽  
Catalytic Performance ◽  
Water Soluble ◽  
Methanol Oxidation Reaction ◽  
Solution Synthesis ◽  
X Ray ◽  
Electrocatalytic Properties

The Pt-Bi (Bi2O3)/GNs (PVP) composite was synthesized using aqueous solution synthesis and characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and Raman spectroscopy. It was found that the water-soluble polyvinyl pyrrolidone (PVP) helped to tune the particles’ morphology, resulting in a uniform distribution of Pt-Bi nanoclusters on the surface of graphene. Cyclic voltammetry, chronoamperometry and linear scanning voltammetry (LSV) were used to study the electrocatalytic properties towards a methanol oxidation reaction (MOR) and an oxygen reduction reaction (ORR). The results show that Pt-Bi (Bi2O3)/GNs (PVP) exhibits superior bifunctional electrocatalytic properties for both MOR and ORR, mainly due to the introduction of oxophilic Bi species and the better dispersion of the Pt-Bi nanoclusters. In particular, the electro-photo catalysis for both MOR and ORR occurred under simulated sunlight irradiation due to the existence of photo-responsive Bi species, which is helpful for converting solar energy into electric energy during a traditional electrocatalytic process.

scholarly journals Oxidation of 5-Hydroxymethylfurfural on Supported Ag, Au, Pd and Bimetallic Pd-Au Catalysts: Effect of the Support

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 115
Author(s):  
Dmitrii German ◽  
Ekaterina Pakrieva ◽  
Ekaterina Kolobova ◽  
Sónia A. C. Carabineiro ◽  
Marta Stucchi ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Bimetallic Catalysts ◽  
Inductively Coupled Plasma ◽  
Noble Metals ◽  
Nitrogen Adsorption ◽  
Carbon Support ◽  
Atomic Emission ◽  
Indicator Method ◽  
X Ray ◽  
Effect Of The Support

Oxidation of 5-hydroxymethylfurfural (HMF), a major feedstock derived from waste/fresh biomass, into 2,5-furandicarboxylic acid (FDCA) is an important transformation for the production of biodegradable plastics. Herein, we investigated the effect of the support (unmodified and modified titania, commercial alumina, and untreated and treated Sibunit carbon) of mono- and bimetallic catalysts based on noble metals (Ag, Au, Pd) on selective HMF oxidation with molecular oxygen to FDCA under mild and basic reaction conditions. The higher selectivity to FDCA was obtained when metals were supported on Sibunit carbon (Cp). The order of noble metal in terms of catalyst selectivity was: Ag < Au < Pd < PdAu. Finally, FDCA production on the most efficient PdAu NPs catalysts supported on Sibunit depended on the treatment applied to this carbon support in the order: PdAu/Cp < PdAu/Cp-HNO3 < PdAu/Cp-NH4OH. These bimetallic catalysts were characterized by nitrogen adsorption-desorption, inductively coupled plasma atomic emission spectroscopy, high resolution transmission electron microscopy, energy dispersive spectroscopy, X-ray diffraction, Hammet indicator method and X-ray photoelectron spectroscopy. The functionalization of Sibunit surface by HNO3 and NH4OH led to a change in the contribution of the active states of Pd and Au due to promotion effect of N-doping and, as a consequence, to higher FDCA production. HMF oxidation catalyzed by bimetallic catalysts is a structure sensitive reaction.

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