Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: KEGG:D01931 (TiO2)
11,320 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

When surface-reactive (bioactive) coatings are applied to medical implants by means of CO2 laser processing, the bioactivity of the surface of the implant can be locally modified to match the properties of the surrounding tissues to provide a firm fixation of the implant. The aim of this study was to compare the heat treated TiO2 coatings with the laser-treated TiO2 coatings in terms of amorphous-crystalline-phase development. The coatings were characterized with thin-film X-ray diffraction (TF-XRD), atomic force microscopy (AFM) and scanning electron microscopy (SEM). The TiO2 coatings heat treated at 500 degrees C known to be bioactive in SBF (simulated body fluid) consisted mainly of anatase with some rutile-phase, suggesting a predominant effect of anatase on reactivity of coatings. However, the coatings preheat-treated at 500 degrees C with further laser treatment exhibited enhanced bioactivity while consisting mainly of rutile. These findings indicated a key role of both rutile and anatase for the reactivity of the coatings. Without preheat treatment, by laser treatment alone, the amorphous titania coatings developed into mixed anatase/rutile containing coatings. This structural organization and the increase in crystal size are thus considered to be the reasons for their bioactivity. The SBF results indicate the possibility to control bioactivity by altering laser power used through the anatase/rutile crystallinity enhancement.
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PMID:TF-XRD examination of surface-reactive TiO2 coatings produced by heat treatment and CO2 laser treatment. 1570 75

Bioactive coatings on cp-Ti and Ti-6Al-4V were prepared by a simple chemical technique. Specimens of cp-Ti and Ti-6Al-4V were initially immersed in a 5 M NaOH solution at 60 degrees C for 24 h which resulted in the formation of a porous network structure composed of Na2Ti5O11 and TiO2. The specimens were then immersed in a Ca-rich solution either at 60 degrees C or at 36.5 degrees C for 24 h. During this treatment Na+ was released and Ti-OH groups were formed. Subsequently, TiO2 dissociated from the Ti-OH group and combined with calcium ions to form calcium titanate (CaTiO3), which was embedded in a titania gel layer during the immersion period. The specimens were then immersed in r-SBF at 36.5 degrees C for 1-30 days. After immersion in r-SBF for 3 days, HAp (hydroxyapatite) spheroids began to deposit on the substrates, and within a week the surfaces were covered. The HAp spheroids were 5 microm in size with a Ca/P ratio of 1.68 which was close to bone-like apatite (1.67). The average thicknesses of HAp layer after immersion in r-SBF for 3 days, 1 week, and 2 weeks were 3.8, 5.6, and 6.4 microm, respectively. A scratch test, used to evaluate the adhesive strength of the HAp layer, showed that the HAp layer was not scraped off until the applied load reached 26 N.
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PMID:Formation of hydroxyapatite layer on bioactive Ti and Ti-6Al-4V by simple chemical technique. 1794 15

The titanium oxide films were fabricated on titanium metal by e-beam deposition technique in various oxygen partial pressures in order to investigate the effects of oxygen content in titanium oxide film on the bioactivity of titanium implant. The nano-sized titanium oxide particles were observed on the surface of specimens. Raman spectra showed that titanium oxide films deposited by e-beam evaporator had oxygen deficient TiO2 structure. The oxygen content in oxide films was calculated from the high resolution XPS spectra of Ti 2p. The densities of HA particles formed on the sample surfaces after immersion test in SBF became higher as the contents of oxygen in titanium oxide films increased. We concluded that the degree of hydroxyl group formation in SBF depended on the stoichiometry of TiO2, which enhanced the bioactivity of titanium.
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PMID:Effects of oxygen content on bioactivity of titanium oxide films fabricated on titanium by electron beam evaporation. 1804 65

Novel organic-inorganic hybrid materials were synthesized by the sol-gel method from a multicomponent solution containing titanium butoxide, 6 weight % (wt%) or 12 wt% poly(ether-imide) (PEI), water and chloroform. The structure of the interpenetrating network is realized by hydrogen bonds between the Ti-OH group (H-donator) in the sol-gel intermediate species and the carboxylic group (H-acceptor) in the repeating units of the polymer. By Fourier transform infrared (FTIR) analysis the presence of hydrogen bonds between organic-inorganic components of the hybrid materials were proved. The morphology of the hybrid materials was studied by scanning electron microscopy (SEM). The structure of a molecular level dispersion was disclosed by an atomic force microscope (AFM), pore size distribution and surface measurements. The AFM and SEM analyzes confirmed that the PEI/TiO2 samples can be considered homogenous organic/inorganic hybrid materials because in both the compositions studied the average domains were less than 400 nm in size. The bioactivity of the synthesized hybrid materials was demonstrated by the formation of a layer of hydroxyapatite on the surface of the PEI/TiO2 samples soaked in a fluid simulating the composition of human blood plasma (SBF), demonstrated by SEM and energy dispersive spectroscopy (EDS) microscopy.
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PMID:Sol-gel synthesis, characterization and bioactivity of poly(ether-imide)/TiO2 hybrid materials. 2079 96

Electrochemical depositions of HAp nanoparticles onto Ultra-fine TiO2 nanotube layer were carried out by the electrochemical reaction in mixed electrolyte of 1.6 M (NH4)H2PO4 + 0.8 M NH4F containing 0.15 and 0.25 wt% HAp. The Ca/P ratios of the HAp nanoparticles were evaluated by EDS analysis and their values were 1.53 and 1.66 respectively. The distribution quantity of Ca and P were remained at the middle region of TiO2 nanotube, but the Ti element was mainly stayed at the bottom of barrier layer from the result of line scanning diagram. Especially, adsorbed phosphate ions facilitated nucleation of nanophase calcium phosphate material inside the TiO2 nanotubu layer that resulted in vertical growth of HAp nanoparticles. These surfaces and structures were all effective for biocompatibility from the SBF tests.
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PMID:Electrodeposition of hydroxyapatite nanoparticles onto ultra-fine TiO2 nanotube layer by electrochemical reaction in mixed electrolyte. 2210 49

Nano- and micro-phase HA film formed on TiO2 nano-network surface by simple electrochemical treatment. The range of lateral pore size of the network specimen was about 10-120 nm on Ti surface by anodized in 5 M NaOH solution at 0.3 A for 10 min. Nano-network TiO2 surface were formed by this anodization step which acted as templates and anchorage for growth of the HA during subsequent pulsed electrochemical deposition process at 85 degrees C. The phase and morphologies of deposits HA were influenced by the electrolyte concentration. The nano needle-like precipitates formed under low SBF concentration were identified to be HA crystals orientated parallel to the c-axis direction. Increasing electrolyte concentration, needle-like deposits transferred to the plate-like and micro plate like precipitates in the case of high SBF concentration.
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PMID:Formation of nano-phase hydroxyapatite film on TiO2 nano-network. 2252 64

This study systematically evaluated the surface and corrosion characteristics of commercially pure titanium (grade 2) modified by plasma electrolytic oxidation (PEO) with high current density. The anodization process was carried out galvanostatically (constant current density) using a solution containing calcium glycerophosphate (0.02mol/L) and calcium acetate (0.15mol/L). The current densities applied were 400, 700, 1000 and 1200mA/cm(2) for a period of 15s. Composition, crystalline structure, morphology, roughness, wettability and "in-vitro" bioactivity test in SBF of the anodized layer were evaluated by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, profilometry and contact angle measurements. Corrosion properties were evaluated by open circuit potential, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization measurements. The results show that the TiO2 oxide layers present an increase of thickness, porosity, roughness, wettability, Ca/P ratio, and bioactivity, with the applied current density up to 1000mA/cm(2). Corrosion resistance also increases with applied current density. It is observed that for 1200mA/cm(2), there is a degradation of the oxide layer. In general, the results suggest that the anodized TiO2 layer with better properties is formed with an applied current of 1000mA/cm(2).
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PMID:Incorporation of Ca and P on anodized titanium surface: Effect of high current density. 2458 43

Most of the research work focussed on fabricating an implant material with an ideal combination of potential bioactivity on the surface and striking mechanical property of bulk in one elementary operation. Interwoven with above concept, SiO2 incorporated nanostructured titania coatings were fabricated on Ti alloy by anodization using sodium silico fluoride electrolyte (SSF). The coatings were characterized by SEM, EDS, AFM, XRD and AT-FTIR techniques. The bioactivity and biocompatibility of the anodic coatings were also investigated. The AT-FTIR, EDS and XRD studies confirm the incorporation of SiO2 into TiO2 coating was confirmed by EDS, XRD and AT-FTIR techniques. The coating formed at the optimum conditions displays a dome like structure with nano flake morphology with maximum mechanical and anticorrosion properties. AFM analysis inferred that the surface roughness of the ceramic coating is higher compared to the pure titania. The SBF test and cell adhesion results predicted that SiO2 incorporated TiO2 coating is superior in their bioactivity compared to TiO2 coating.
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PMID:Fabrication of TiO2-SiO2 bioceramic coatings on Ti alloy and its synergetic effect on biocompatibility and corrosion resistance. 2581 8

TiO2 nanotube arrays were synthesized on Ti surface by anodic oxidation. The elements of Ca and P were simultaneously incorporated during nanotubes growth in SBF electrolyte, and then Ag was introduced to nanotube arrays by cathodic deposition, which endowed the good osseointegration and antibacterial property of Ti. The bioactivity of the Ti surface was evaluated by simulated body fluid soaking test. The biocompatibility was investigated by in vitro cell culture test. And the antibacterial effect against Staphylococcus aureus was examined by the bacterial counting method. The results showed that the incorporation of Ca, P and Ag elements had no significant influence on the formation of nanotube arrays on Ti surface during electrochemical treatment. Compared to the polished or nanotubular Ti surface, TiO2 nanotube arrays incorporated with Ca, P and Ag increased the formation of bone-like apatite in simulated body fluid, enhanced cell adhesion and proliferation, and inhibited the bacterial growth. Based on these results, it can be concluded that the nanostructured Ti incorporated with Ca, P and Ag by electrochemical method has promising applications as implant material.
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PMID:Biological properties of nanostructured Ti incorporated with Ca, P and Ag by electrochemical method. 2584 11

Poly(vinyl alcohol) (PVA) is reinforced with TiO2 nanoparticles in order to enhance thermo-mechanical stabilities, surface characteristics and osteoblastic cell adhesion. PVA-TiO2 nanocomposite films with desirable mechanical, thermal and biocompatible properties are fabricated through solution casting method followed by de-hydrothermal cross-linking treatment. The composition of TiO2 nanoparticles was standardized to achieve mechanically stable nanocomposite films, based on tensile strength measurements composition of TiO2 is determined as optimal at 3wt%. PVA-TiO2 nanocomposite films were characterized by Scanning electron microscopy, Energy dispersive spectroscopy, Atomic force microscopy, Ultra violet and Fourier transform infrared spectroscopic techniques. Elemental mapping studies substantiate incorporation of TiO2 nanoparticles within the PVA matrix. Dimensional stability evaluated by soaking films in SBF for 24h insinuates the role of TiO2 in the direction of controlling degree of swelling. In-vitro bioactivity test and cell adhesion results also predict that presence of TiO2 is advantageous to enhance apatite growth and promote cell-substrate interaction. SEM studies illustrate improved surface morphology of PVA-TiO2 nanocomposite film with homogenously distributed TiO2 nanoparticles, which help to enhance thermo-mechanical behavior. TiO2 nanoparticles construct cell-adhesive hydrophilic nano-domains that act as potential cell adhesion sites and promotes osteointegration. Bio compatibility studies proved that thermally cross-linked PVA is non-toxic in relation to PVA cross-linked with glutaraldehyde. Cytotoxicity and cell adhesion of nanocomposite films evaluated through cell viability (MMT) assay and crystal violet staining revealed that PVA-3wt% TiO2nanocomposite could act as an excellent composite and hence suitable to be used in bone implant applications.
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PMID:Fabrication and characterization of poly(vinyl alcohol)-TiO2 nanocomposite films for orthopedic applications. 2737 70


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