Search results for "Photochemical Processes"

showing 10 items of 50 documents

Photogenotoxicity of folic acid.

2013

Folic acid (FA), also named vitamin B9, is an essential cofactor for the synthesis of DNA bases and other biomolecules after bioactivation by dihydrofolate reductase (DHFR). FA is photoreactive and has been shown to generate DNA modifications when irradiated with UVA (360 nm) in the presence of DNA under cell-free conditions. To investigate the relevance of this reaction for cells and tissues, we irradiated three different cell lines (KB nasopharyngeal carcinoma cells, HaCaT keratinocytes, and a melanoma cell line) in the presence of FA and quantified cytotoxicity and DNA damage generation. The results indicate that FA is phototoxic and photogenotoxic by two different mechanisms. First, ext…

DNA damageCell SurvivalAntineoplastic AgentsBiochemistrychemistry.chemical_compoundFolic AcidPhysiology (medical)Cell Line TumorDihydrofolate reductaseHumansCell ProliferationbiologyDNA synthesisChemistrySuperoxide DismutaseCatalasePhotochemical ProcessesNuclear DNAHaCaTTetrahydrofolate DehydrogenaseMethotrexateBiochemistryDNA glycosylaseCell culturebiology.proteinFolic Acid AntagonistsDrug Screening Assays AntitumorDNADNA DamageFree radical biologymedicine
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DNA binding, nuclease activity, DNA photocleavage and cytotoxic properties of Cu(II) complexes of N-substituted sulfonamides.

2013

Abstract Ternary copper(II) complexes [Cu(NST)2(phen)] (1) and [Cu(NST)2(NH3)2]·H2O (2) [HNST = N-(4,5-dimethylthiazol-2-yl)naphthalene-1-sulfonamide] were prepared and characterized by physico-chemical techniques. Both 1 and 2 were structurally characterized by X-ray crystallography. The crystal structures show the presence of a distorted square planar CuN4 geometry in which the deprotonated sulfonamide, acting as monodentate ligand, binds to the metal ion through the thiazole N atom. Both complexes present intermolecular π–π stacking interactions between phenanthroline rings (compound 1) and between naphthalene rings (compound 2). The interaction of the complexes with CT DNA was studied b…

DenticityStereochemistryCell SurvivalUltraviolet RaysPhenanthrolineRadicalStackingAscorbic AcidNaphthalenesBiochemistryFluorescence spectroscopyInorganic Chemistrychemistry.chemical_compoundInhibitory Concentration 50Coordination ComplexesCell Line TumorAnimalsHumansDNA CleavageThiazoleNucleaseSulfonamidesBinding SitesbiologyCytotoxinsHydroxyl RadicalDNAHydrogen PeroxidePhotochemical ProcessesKineticschemistrybiology.proteinCattleDNACopperPhenanthrolinesJournal of inorganic biochemistry
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Keggin heteropolyacid H3PW12O40 supported on different oxides for catalytic and catalytic photo-assisted propene hydration

2013

Catalytic and catalytic photo-assisted hydration of propene to form 2-propanol in gas–solid regime at atmospheric pressure and 85 1C were carried out by using a heteropolyacid (POM) supported on different oxides. Binary materials were prepared by impregnation of H3PW12O40 on different commercial and home prepared supports (TiO2, SiO2, WO3, ZrO2, ZnO, Al2O3). Some of the composites were active both for catalytic and catalytic photo-assisted reactions. The Keggin type POM was completely and partially degraded, when supported on ZnO and Al2O3, respectively, and these binary solids always resulted as inactive for both catalytic and catalytic photo-assisted reactions. The supported Keggin POM sp…

DiffractionDiffuse reflectance infrared fourier transformAtmospheric pressureSurface PropertiesScanning electron microscopeWaterGeneral Physics and AstronomyOxidesAlkenesPhotochemical ProcessesPhotochemistryCatalysisTungstenCatalysisPropenechemistry.chemical_compoundchemistryPressureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesense organsIrradiationKeggin heteropolyacid catalytic propene hydration photo-assisted propene hydrationParticle SizePhysical and Theoretical ChemistryFourier transform infrared spectroscopyPhysical Chemistry Chemical Physics
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Features and application of coupled cold plasma and photocatalysis processes for decontamination of water

2020

Dielectric barrier discharge plasma and photocatalysis have been proposed as tools for decontamination of process water, especially in food industry. The present investigation aims to redefine and identify the features of coupling the two technologies in terms of degradation efficiency of a model compound. Results show that, when the process is carried out in plasma activated water in the presence of irradiated TiO2, the efficiency of the integrated process is lower than the sum of the two processes acting separately. It is proposed that afterglow species, e.g. hydrogen peroxide and/or peroxynitrites could be activated by UVA light irradiation producing hydroxyl radicals in the liquid phase…

Environmental EngineeringMaterials sciencePlasma GasesUltraviolet RaysHealth Toxicology and MutagenesisRadical0208 environmental biotechnology2UVA light02 engineering and technologyDielectric barrier discharge010501 environmental sciencesDielectric barrier discharge plasma01 natural sciencesCatalysisWater Purificationchemistry.chemical_compoundphotocatalysiTiOWater decontaminationEnvironmental ChemistryIrradiationFood-Processing IndustryHydrogen peroxide0105 earth and related environmental sciencesTitaniumHydroxyl RadicalPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryHuman decontaminationPlasmaEquipment DesignHydrogen PeroxidePhotochemical ProcessesPollution020801 environmental engineeringMethylene BluechemistryChemical engineeringProcess intensificationPhotocatalysisDegradation (geology)Water Pollutants Chemical
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A survey of photocatalytic materials for environmental remediation

2012

Abstract Heterogeneous photocatalysis is an advanced oxidation process which has been the subject of a huge amount of studies related to air cleaning and water purification. All these processes have been carried out mainly by using TiO 2 -based materials as the photocatalysts and ca. 75% of the articles published in the last 3 years is related to them. This review illustrates the efforts in the search of alternative photocatalysts that are not based on TiO 2 , with some exceptions concerning particularly innovative modifications as nanoassembled TiO 2 or TiO 2 composites with active carbon, graphite and fullerene. Papers reporting preparation, characterization and testing of binary, ternary…

Environmental EngineeringMaterials scienceUltraviolet RaysEnvironmental remediationHealth Toxicology and MutagenesisPortable water purificationNanotechnologyCatalysisEnvironmental ChemistryGraphiteWaste Management and DisposalEnvironmental Restoration and RemediationTitaniumNanotubes CarbonAdvanced oxidation processOxidesMineralization (soil science)Photochemical ProcessesPollutionNanostructuresCharacterization (materials science)Environmental chemistryHeterogeneous photocatalysis photocatalysts not based on TiO2PhotocatalysisEnvironmental PollutantsWater treatmentSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Iodide-Photocatalyzed Reduction of Carbon Dioxide to Formic Acid with Thiols and Hydrogen Sulfide.

2016

The photolysis of iodide anions promotes the reaction of carbon dioxide with hydrogen sulfide or thiols to quantitatively yield formic acid and sulfur or disulfides. The reaction proceeds in acetonitrile and aqueous solutions, at atmospheric pressure and room temperature by irradiation using a low-pressure mercury lamp. This transition-metal-free photocatalytic process for CO2 capture coupled with H2 S removal may have been relevant as a prebiotic carbon dioxide fixation.

FormatesFormic acidGeneral Chemical EngineeringHydrogen sulfideInorganic chemistryIodidechemistry.chemical_element010402 general chemistryIodine01 natural sciencesCatalysisCatalysisReaccions químiqueschemistry.chemical_compoundEnvironmental ChemistryGeneral Materials ScienceHydrogen SulfideSulfhydryl Compoundschemistry.chemical_classification010405 organic chemistryCarbon fixationCarbon DioxideIodidesPhotochemical ProcessesSulfur0104 chemical sciencesGeneral EnergychemistryCarbon dioxideQuímica orgànicaOxidation-ReductionChemSusChem
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Substrate templating guides the photoinduced reaction of C60on calcite

2014

cited By 7; International audience; A substrate-guided photochemical reaction of C60 fullerenes on calcite, a bulk insulator, investigated by non-contact atomic force microscopy is presented. The success of the covalent linkage is evident from a shortening of the intermolecular distances, which is clearly expressed by the disappearance of the moiré pattern. Furthermore, UV/Vis spectroscopy and mass spectrometry measurements carried out on thick films demonstrate the ability of our setup for initiating the photoinduced reaction. The irradiation of C60 results in well-oriented covalently linked domains. The orientation of these domains is dictated by the lattice dimensions of the underlying c…

Fullerenescanning probe microscopysurface chemistry02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesChemical reaction530CatalysisCalcium CarbonateScanning probe microscopychemistry.chemical_compoundSpectroscopyCalcite[PHYS]Physics [physics]Spectrum AnalysisIntermolecular forcefullerenesGeneral Chemistrycovalent networksself-assemblyPhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographychemistryChemical physicsCovalent bondSelf-assembly0210 nano-technology
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Study of the Mode and Efficiency of DNA Binding in the Damage Induced by Photoactivated Water Soluble Porphyrins

2013

We have investigated the DNA binding interactions and in vitro photoactivated DNA damage induced by a neutral water soluble porphyrin derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrin (TTHPP) and its zinc derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrinato zinc(II) (Zn-TTHPP) upon visible light irradiation through various spectroscopic techniques and employing repair endonucleases. These porphyrin derivatives exhibited high affinity toward DNA through groove binding interactions as evidenced through the UV-vis absorption, emission, circular dichroism spectral and viscosity changes. Interestingly, the free base porphyrin derivative, TTHPP generated efficient sing…

HematoporphyrinCircular dichroismPorphyrinsSinglet oxygenDNA damageCircular DichroismSpectrum AnalysisWaterDNAGeneral MedicinePhotochemical ProcessesPhotochemistryBiochemistryPorphyrinchemistry.chemical_compoundchemistryDNA glycosylasePhotosensitizerPhysical and Theoretical ChemistryDNADNA DamagePhotochemistry and Photobiology
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Photochemical electrocyclisation of 3-vinylindoles to pyrido[2,3-a]-, pyrido[4,3-a]- and thieno[2,3-a]-carbazoles: Design, synthesis, DNA binding and…

2009

In the context of the design and synthesis of DNA ligands, some new hetarene annelated carbazoles were synthesized. As lead structure the intercalating tetracyclic systems pyrido[2,3-a]- and pyrido[4,3-a]-carbazoles and in one case a thieno[2,3-a]-carbazole were taken into account. A dialkyl amino amidic chain was introduced to the planar chromophoric system with the intent to generate minor groove binding properties. The cytotoxicity of some compounds was examined by the NCI antitumor screening. Furthermore, biophysical as well as biochemical studies were performed in order to get some information about the DNA-binding properties and inhibition of DNA related functional enzymes of this new…

IndolesCell SurvivalStereochemistryCarbazolesFluorescence spectrometryAntineoplastic AgentsStereoisomerismContext (language use)Nucleic Acid DenaturationChemical synthesisFluorescenceStructure-Activity RelationshipCell Line TumorDrug DiscoveryAnimalsHumansTopoisomerase II InhibitorsTransition TemperatureStructure–activity relationshipBinding siteCell ProliferationPharmacologyBinding SitesbiologyChemistryCircular DichroismTopoisomeraseCell CycleOrganic ChemistryStereoisomerismDNAGeneral MedicinePhotochemical ProcessesDNA Minor Groove BindingCyclizationDrug Designbiology.proteinCattleSpectrophotometry UltravioletTopoisomerase I InhibitorsEuropean Journal of Medicinal Chemistry
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Fluorescence emission and enhanced photochemical stability of Zn(II)-5-triethyl ammonium methyl salicylidene ortho-phenylendiiminate interacting with…

2010

Abstract The photophysical and photochemical properties of the cationic Zn II complex of 5-triethyl ammonium methyl salicylidene ortho-phenylendiimine (ZnL 2+ ) interacting with native DNA were investigated by steady state and time-resolved fluorescence spectroscopies. Experimental results indicate that, in the presence of DNA, ZnL 2+ is efficiently protected from a photochemical process, which occurs when it is in the free state dispersed in aqueous solution. The analysis of the absorption and emission spectra of ZnL 2+ , both stored in the dark and after exposure to tungsten lamp light for 24 h, corroborated by quantum chemical calculations, allowed us to point out that ZnL 2+ undergoes a…

Intercalation (chemistry)Context (language use)PhotochemistryBiochemistryFluorescence spectroscopyFluorescenceInorganic ChemistrySchiff baseIntercalationOrganometallic CompoundsMoleculeFluorescence spectroscopyPhotooxidationSettore CHIM/02 - Chimica FisicaAqueous solutionChemistrySpectrum AnalysisDNAPhotochemical ProcessesFluorescenceIntercalating AgentsSolventZincSettore CHIM/03 - Chimica Generale E InorganicaSolventsSteady state (chemistry)Oxidation-ReductionJournal of inorganic biochemistry
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