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)

The possible carcinogenic or fibrogenic effects of intratracheal instillation of a polycyclic hydrocarbon, benzo(a) pyrene (B(a)P), alone or in combination with several dusts - titanium dioxide (TiO2), aluminum oxide (Al2O3), carbon (C), and ferric oxide (Fe3O3) - were investigated in hamsters. When administered alone, the dusts induced interstitial cell proliferation, bronchial epithelial alterations and a few granulomatous changes in the pulmonary system, but no tumors. B(a)P alone induced only two tracheal papillomas. However, combined treatment with B(a)P and the dusts caused a number of tumors, dependent upon the dust used. B(a)P plus TiO2 in a small particle size (below 0.5mu) induced papillomas, squamous cell carcinomas and a few adenomas and adenocarcinomas of the larynx, trachea and lungs. These were morpholoigcally similar to neoplasms found after B(a)P and Fe2O3 treatment. B(a)P, combined with C or Al2O3, induced mainly laryngeal and tracheal papillomas. B(a)P- and C-treated hamsters also showed a few lung adenocarcinomas.
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PMID:Carcinogenicity of Benzo(a)pyrene and dusts in the hamster lung (instilled intratracheally with titanium oxide, aluminum oxide, carbon and ferric oxide). 98 Mar 65

The ability of different mineral fibres to induce morphological transformation of Syrian hamster embryo cells has been studied. Increased transformation frequencies were obtained in the presence of chrysotile, crocidolite, amosite, anthophyllite and the glass fibres (GF) 100, while no significant increase in transformation frequency was observed with GF 110 and TiO2. Chrysotile was the most potent of the fibres tested. GF 100 was more potent than crocidolite, amosite and anthophyllite. By comparing transformation frequency and toxicity, it could be concluded that induction of transformation is not caused by unspecific cytotoxic effects. In contrast to some earlier studies, no synergistic effect was observed between benzo[a]pyrene (BaP) and asbestos fibres. Adsorption of BaP to crocidolite fibres had no effect on the transformation frequency. Moreover, crocidolite was not able to promote the transformation of cells pre-exposed to BaP. Electron microscopy studies showed that the fibres were rapidly phagocytosed. Blebs were often formed on the cell surface and were most pronounced after crocidolite exposure. The blebs did not seem to be associated with the areas of physical interaction between the cells and the fibres, but were distributed throughout the cell surface.
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PMID:Morphological transformation of Syrian hamster embryo cells induced by mineral fibres and the alleged enhancement of benzo[a]pyrene. 283 6

The photocatalytic oxidation of pyrene preadsorbed on TiO2 is examined in aqueous suspension under UV irradiation. Chemical oxygen demand measurements, UV-VIS spectrophotometer, infrared spectrometer and GC-MS analytical techniques were used to monitor the formed intermediates. During the oxidation processes, the ring-open reaction, hydroxylation and ketolysis occurred to produce some intermediate products (4-oxapyrene-5-one, 1,6- or 1,8-pyrenediones, 4,5-phenanthrenedialdehyde, cyclopenta[def]phenanthrene). Some factors affecting the photodegradation rate were also studied. The results were different from other studies: The pH of the dispersion, ratio of Py/TiO2:water had little effect on the photooxidation rate of pyrene catalyzed by TiO2, while the surface coverage, addition of Fe3+ affected it greatly.
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PMID:Photocatalytic reactions of pyrene at TiO2/water interfaces. 1265 36

Small particles of TiO2 have been synthesized on porous silica. XRD and spectral measurements place the sizes of the particles at about 50 A. With these small particles the band gap of the semiconductor material is markedly blue shifted with respect to bulk TiO2. This enables the direct excitation of co-adsorbed arenes on the TiO2-SiO2 material. Direct excitation of TiO2 leads to Ti3+, by photoinduced extraction from the SiO2. Direct excitation of pyrene on the material leads to a shortened fluorescence lifetime and lower quantum yield. Meanwhile, the yield of pyrene cation radical increases compared to that on pure SiO2. The production of Ti3+ on the pyrene samples, by direct excitation of the TiO2, leads to a shortened pyrene fluorescence lifetime and decreased quantum yield, the quantum yield decreasing to zero at high enough Ti3+. Removal of Ti3+ by O2 causes the original properties of the pyrene fluorescence to return.
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PMID:Photoinduced electron transfer at solid surfaces: the TiO2-SiO2 system. 1460 57

Phenylenethynylene (PE) rigid linkers (para and meta) were used to anchor pyrene to the surface of TiO2 (anatase) and ZrO2 nanoparticle thin films through the two COOH groups of an isophthalic acid (Ipa) unit. Four chromophore-linker models were studied in solution and bound. Two are novel meta-pyrene-PE linker systems: dimethyl 5-(3-(1-pyrenylethynyl)phenylethynyl)-isophthalate, carrying one pyrene, and dimethyl 5-(bis-3,5-(1-pyrenylethynyl)phenylethynyl)-isophthalate, carrying two. These were compared with para rigid-rods dimethyl 5-(1-pyrenylethynyl)isophthalate and dimethyl 5-(4-(1-pyrenylethynyl)phenylethynyl)-isophthalate, each carrying one pyrene but varying in length. The length of the PE linkers and the para or meta substitution influence the photophysical properties of the compounds. The extinction coefficient increased, and the long wavelength absorbance of the pyrene chromophore was shifted to the red with increasing conjugation. Compared to unsubstituted pyrene, the pyrene-linker systems were characterized by short fluorescence lifetimes (tau approximately 2 ns in tetrahydrofuran solutions), but quantum yields were close to unity. ZINDO/S CI calculations attribute this effect to a switching in the order of the two lowest-lying singlet states of pyrene. High surface coverages, approximately 10(-8) mol/cm2, and carboxylate binding modes on nanostructured TiO2 films were obtained in all cases. The appearance of a pyrene excimer emission on ZrO2, an insulator, indicates that the pyrene-linker system is closely packed (Py-Py < 4 A) on the surface. The fluorescence emission on TiO2 was completely quenched, consistent with quantitative and rapid electron injection into the semiconductor indicating that the pyrene excimer acts as a sensitizer. Photoelectrochemical studies in regenerative solar cells with I3-/I- as the redox mediator indicated near-quantitative conversion of absorbed photons into an electrical current.
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PMID:Pyrene-terminated phenylenethynylene rigid linkers anchored to metal oxide nanoparticles. 1689 19

The rates of photodegradation and photocatalysis of benzo[a]pyrene (BaP) on soil surfaces under UV light have been studied. Different parameters such as temperature, soil particle sizes, and soil depth responsible for photodegradation, catalyst loads and wavelength of UV irradiation blamed for photocatalysis have been monitored. The results obtained indicated that BaP photodegradation follows pseudo-first-order kinetics. BaP photodegradation was the fastest at 30 degrees C . The rates of BaP photodegradation at different soil particle size followed the order: less than 1 mm>less than 0.45 mm>less than 0.25 mm. When the soil depth increased from 1 mm to 4 mm, the half-life increased from 13.23 d to 17.73 d. The additions of TiO2 or Fe2O3 accelerated the photodegradation of BaP, and the photocatalysis of BaP follows pseudo-first-order kinetics. Changes in catalyst loads of TiO2 (0.5%, 1%, 2%, and 3% (wt)) or Fe2O3 (2%, 5%, 7%, and 10% (wt)) did not significantly affect the degradation rates. Both BaP photocatalysis in the presence of TiO2 and Fe2O3 were the fastest at 254 nm UV irradiation.
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PMID:Photochemical behavior of benzo[a]pyrene on soil surfaces under UV light irradiation. 1729 70

To improve the knowledge of the underlying mechanisms of action involved in air pollution Particulate Matter (PM)-induced toxicity in human lungs, with a particular interest of the crucial role played by coated-organic chemicals, we were interested in the metabolic activation of Polycyclic Aromatic Hydrocarbons (PAH)-coated onto air pollution PM, and, thereafter, the formation of PAH-DNA adducts in a human lung epithelial cell model (A549 cell line). Cells were exposed to Dunkerque city's PM(2.5) at its Lethal Concentrations at 10% and 50% (i.e. LC(10)=23.72 microg/mL or 6.33 microg/cm2, and LC(50)=118.60 microg/mL or 31.63 microg/cm2), and the study of Cytochrome P450 (CYP) 1A1 gene expression (i.e. RT-PCR) and protein activity (i.e. EROD activity), and the formation of PAH-DNA adducts (i.e. 32P-postlabeling), were investigated after 24, 48, and/or 72 h. PAH, PolyChlorinated Dibenzo-p-Dioxins and -Furans (PCDD/F), Dioxin-Like PolyChlorinated Biphenyls (DLPCB), and PolyChlorinated Biphenyls (PCB)-coated onto collected PM were determined (i.e. GC/MS and HRGC/HRMS, respectively), Negative (i.e. TiO2 or desorbed PM, dPM; EqLC10=19.42 microg/mL or 5.18 microg/cm2, and EqLC50=97.13 microg/mL or 25.90 microg/cm2), and positive (i.e. benzo(a)pyrene; 1 microM) controls were included in the experimental design. Statistically significant increases of CYP1A1 gene expression and protein activity were observed in A549 cells, 24, 48 and 72 h after their exposure to dPM, suggesting thereby that the employed outgassing method was not efficient enough to remove total PAH. Both the CYP1A1 gene expression and EROD activity were highly induced 24, 48 and 72 h after cell exposure to PM. However, only very low levels of PAH-DNA adducts, also not reliably quantifiable, were reported 72 h after cell exposure to dPM, and, particularly, PM. The relatively low levels of PAH together with the presence of PCDD/F, DLPCB, and PCB-coated onto Dunkerque City's PM 2.5 could notably contribute to explain the borderline detection of PAH-DNA adducts in dPM and/or PM-exposed A549 cells. Hence, remaining very low doses of PAH in dPM or relatively low doses of PAH-coated onto PM were involved in enzymatic induction, a key feature in PAH-toxicity, but failed to show a clear genotoxicity in this in vitro study. We also concluded that, in the human lung epithelial cell model we used, and in the experimental conditions we chose, bulky-DNA adduct formation was apparently not a major factor involved in the Dunkerque City's PM 2.5-induced toxicity.
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PMID:Genotoxic potential of Polycyclic Aromatic Hydrocarbons-coated onto airborne Particulate Matter (PM 2.5) in human lung epithelial A549 cells. 1855 80

Sensitization and binding of a large footprint pyrene chromophore to planar (sapphire) and colloidal metal oxide films (TiO2 and ZrO2) is investigated. The model compound combines a 1-pyrenyl-ethynylenephenylene unit with a new adamantane-tripodal linker that binds to the surface. The linker design, combining a large footprint (approximately 2 nm2) of the tripodal linker with the meta position of the COOH anchoring groups, was suggested from atomistic models, and it aims to provide improved spacing control. The pyrene chromophore unit provides a probe of sensitizer-sensitizer interactions through its propensity to form excimers, unless neighboring pyrene units are sufficiently spaced (>or=3.5 A). Absorption and fluorescence studies, and a comparison with a pyrene-rigid rod model compound, suggest that the new tripodal anchor group allows spacing control on planar surfaces. On colloidal films, the linker provides spacing control at low surface coverage but sensitizer-sensitizer interactions are still observed on colloidal films at high surface coverage. Implications for the functionalization of metal oxide films in hybrid molecule-metal oxide semiconductor material systems are discussed.
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PMID:Large footprint pyrene chromophores anchored to planar and colloidal metal oxide thin films. 1971 22

Pyrene chromophores carrying different rigid rod spacer groups (ethynylene, ethynylene-phenylene-ethynylene, and ethynylene-bicyclo[2.2.2]octylene-ethynylene) and bound to TiO2 nanostructured materials via an isophthalic acid (Ipa) anchor group have been investigated using quantum chemical calculations in order to elucidate structural and electronic properties of dye-sensitized semiconductor structures capable of long-range photoinduced interfacial electron transfer. The calculations are used to study firstly the effect of the anchor and spacer groups on the electronic properties of the pyrene-dyes, secondly the binding of isophthalic acid to nanostructured TiO2, and thirdly the interfacial electronic interactions for dye-sensitized nanostructured TiO2 relevant to dye-sensitized solar cell applications. Together, these calculations provide theoretical insights into the effect of incorporating rigid rod anchor-cum-spacer group motifs in sensitizers for e.g. solar cell applications. In particular, the calculations help to rationalize the strong influence of the rods on the photophysical properties of the sensitizers in terms of electronic interactions between the individual chromophore, spacer, and anchor segments, as well as to provide information about interfacial electronic interactions of interest for the capabilities of the rods to act as efficient mediators of photoinduced interfacial charge separation.
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PMID:Calculations of interfacial interactions in pyrene-Ipa rod sensitized nanostructured TiO2. 1990 29

An analytical method based on TiO2 nanotubes solid-phase extraction (SPE) combined with gas chromatography (GC) was established for the analysis of seven polycyclic aromatic hydrocarbons (PAHs): acenaphtylene, acenaphthene, anthracene, fluorene, phenanthrene, fluoranthene and pyrene. Factors affecting the extraction efficiency including the eluent type and its volume, adsorbent amount, sample volume, sample pH and sample flow rate were optimized. The characteristic data of analytical performance were determined to investigate the sensitivity and precision of the method. Under the optimized extraction conditions, the method showed good linearity in the range of 0.01-0.8 microg/mL, repeatability of the extraction (RSD were between 6.7% and 13.5%, n = 5) and satisfactory detection limits (0.017-0.059 ng/mL). The developed method was successfully applied to the analysis of surface water (tap, river and dam) samples. The recoveries of PAHs spiked in environmental water samples ranged from 90% to 100%. All the results indicated the potential application of titanate nanotubes as solid-phase extraction adsorbents to pre-treat water samples.
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PMID:TiO2 nanotubes as solid-phase extraction adsorbent for the determination of polycyclic aromatic hydrocarbons in environmental water samples. 2179 61


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