Search results for "Singlet Oxygen"

showing 10 items of 62 documents

Dynamics of Singlet Oxygen Molecule Trapped in Silica Glass Studied by Luminescence Polarization Anisotropy and Density Functional Theory

2020

The support from M-ERANET project “MyND” is acknowledged. A.A., M.M-S., and L.R. were supported by the Research Council of Lithuania (Grant M-ERA.NET-1/2015). The authors thank A. Pasquarello for providing the structures of the amorphous SiO 2 matrix for our computational work and K. Kajihara (Tokyo Metropolitan University) for valuable advice in PL kinetics measurements.

Materials science02 engineering and technology010402 general chemistryCondensed Matter::Disordered Systems and Neural Networks7. Clean energy01 natural sciencesMolecular physicschemistry.chemical_compound:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryPolarization (electrochemistry)AnisotropySinglet oxygenDynamics (mechanics)021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed MatterGeneral EnergyPhotobiologychemistry13. Climate actionDensity functional theory0210 nano-technologyLuminescenceThe Journal of Physical Chemistry C
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Fe3O4@Au@mSiO2 as an enhancing nanoplatform for Rose Bengal photodynamic activity

2017

A novel nanoplatform composed of three types of materials with different functionalities, specifically core-shell Fe3O4@Au nanoparticles encapsulated near the outer surface of mesoporous silica (mSiO2) nanoparticles, has been successfully synthesised and used to enhance the efficiency of a photosensitiser, namely Rose Bengal, in singlet oxygen generation. Fe3O4 is responsible for the unusual location of the Fe3O4@Au nanoparticle, while the plasmonic shell acts as an optical antenna. In addition, the mesoporous silica matrix firmly encapsulates Rose Bengal by chemical bonding inside the pores, thus guaranteeing its photostability, and in turn making the nanosystem biocompatible. Moreover, th…

Materials scienceRose-BengalSinglet-OxygenNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciences//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundOptical antennaOn demandRose bengal//purl.org/becyt/ford/1.4 [https]General Materials ScienceSinglet oxygenOtras Ciencias QuímicasNanoplataformCiencias QuímicasMesoporous silica021001 nanoscience & nanotechnologyBiocompatible material0104 chemical scienceschemistry0210 nano-technologyCIENCIAS NATURALES Y EXACTAS
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NIR excitation of upconversion nanohybrids containing a surface grafted Bodipy induces oxygen-mediated cancer cell death

2020

We report the preparation of water-dispersible, ca. 30 nm-sized nanohybrids containing NaYF4:Er3+, Yb3+ up-conversion nanoparticles (UCNPs), capped with a polyethylene glycol (PEG) derivative and highly loaded with a singlet oxygen photosensitizer, specifically a diiodo-substituted Bodipy (IBDP). The photosensitizer, bearing a carboxylic group, was anchored to the UCNP surface and, at the same time, embedded in the PEG capping; the combined action of the UCNP surface and PEG facilitated the loading for an effective energy transfer and, additionally, avoided photosensitizer leaching from the nanohybrid (UCNP-IBDP@PEG). The effectiveness of the nanohybrids in generating singlet oxygen after n…

Materials scienceSinglet oxygentechnology industry and agricultureBiomedical Engineeringchemistry.chemical_elementNanoparticleGeneral ChemistryGeneral MedicinePolyethylene glycolPhotochemistryOxygenPhoton upconversionchemistry.chemical_compoundchemistryPEG ratioGeneral Materials SciencePhotosensitizerBODIPYJ. Mater. Chem. B
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Adducts of free-base meso-tetraarylporphyrins with trihaloacetic acids: Structure and photostability

2020

Abstract Four diverse meso-tetraarylporphyrins in the form of diprotonated adducts with trifluoro-, trichloro-, tribromoacetic acids and acetic acid were investigated in benzene solution. Despite similar structural distortion of the chromophore system due to protonation, the respective adducts demonstrated different photostability when exposed to UV irradiation. The trifluoro- and trichloroacetic adducts, and the acetic acid one, showed some common features both molecular and in the mechanism of photodegradation. However, the tribromo-derivative decayed according to a different kinetic scheme, revealing a considerable impact of the bromine atoms upon the pyrrole units of the porphyrin macro…

Meso-tetraarylporphyrinsSinglet oxygenGeneral Chemical EngineeringGeneral Physics and AstronomyFree baseProtonation02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryDFT calculations01 natural sciencesPorphyrinTrihaloacetic acids0104 chemical sciencesAdductPorphyrin protonationchemistry.chemical_compoundAcetic acidchemistry0210 nano-technologyPhotodegradationPyrroleJournal of Photochemistry and Photobiology A-Chemistry
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Copper-mediated DNA photocleavage by a tetrapyridoacridine (tpac) ligand.

2008

Abstract We have focused our interest on the tetrapyridoacridine ligand tetrapyrido[3,2- a :2′,3′- c :3′′,2″- h : 2‴,3‴- j ]acridine (tpac), as a model system for the preparation of novel copper-based artificial nucleases. The complex of copper(II)–tpac cleaves supercoiled pUC18 plasmid DNA in an oxidative manner by photoactivation with visible light, exhibiting maximum cleaving efficiency at 1:2 metal–ligand stoichiometric ratio. We propose an interaction of the copper–tpac complex with DNA through both major and minor grooves and a photocleavage mechanism via the formation of hydroxyl radicals and singlet oxygen or singlet oxygen-like species.

Models MolecularLightStereochemistryPhotochemistryRadicalClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementPhotochemistryLigandsBiochemistrychemistry.chemical_compoundPolycyclic compoundDrug DiscoveryPhotosensitizerSinglet stateMolecular Biologychemistry.chemical_classificationDeoxyribonucleasesMolecular StructureSinglet OxygenChemistrySinglet oxygenOrganic ChemistryDNACopperAcridineMolecular MedicineAcridinesDNACopperPhenanthrolinesBioorganicmedicinal chemistry letters
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Chemical and photochemical properties of chloroharmine derivatives in aqueous solutions

2015

Thermal and photochemical stability (ΦR), room temperature UV-vis absorption and fluorescence spectra, fluorescence quantum yields (ΦF) and lifetimes (τF), quantum yields of hydrogen peroxide (ΦH2O2) and singlet oxygen (ΦΔ) production, and triplet lifetimes (τT) have been obtained for the neutral and protonated forms of 6-chloroharmine, 8-chloroharmine and 6,8-dichloroharmine, in aqueous media. When it was possible, the effect of pH and oxygen concentration was evaluated. The nature of electronic transitions of protonated and neutral species of the three investigated chloroharmines was established using Time-Dependent Density Functional Theory (TD-DFT) calculations. The impact of all the fo…

PHOTOCHEMICALGeneral Physics and Astronomychemistry.chemical_elementProtonationTriplet lifetime02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesOxygenFluorescence//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCHLOROHARMINE//purl.org/becyt/ford/1.4 [https]MoleculePhysical and Theoretical ChemistryAqueous solutionSINGLET OXYGENMolecular StructureChemistrySinglet oxygenPhotochemicalSinglet oxygenOtras Ciencias QuímicasTRIPLET LIFETIMECiencias QuímicasWaterHydrogen PeroxideQuímica021001 nanoscience & nanotechnologyPhotochemical Processes0104 chemical sciencesOxygenSolutionsHarmineSpectrometry FluorescenceAtomic electron transitionChloroharmineDensity functional theoryAbsorption (chemistry)0210 nano-technologyCIENCIAS NATURALES Y EXACTAS
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Synthesis and photocytotoxic activity of [1,2,3]triazolo[4,5-h][1,6]naphthyridines and [1,3]oxazolo[5,4-h][1,6]naphthyridines

2018

Abstract [1,2,3]Triazolo[4,5-h][1,6]naphthyridines and [1,3]oxazolo[5,4-h][1,6]naphthyridines were synthesized with the aim to investigate their photocytotoxic activity. Upon irradiation, oxazolo-naphtapyridines induced light-dependent cell death at nanomolar/low micromolar concentrations (EC50 0.01–6.59 μM). The most photocytotoxic derivative showed very high selectivity and photocytotoxicity indexes (SI = 72–86, PTI>5000), along with a triplet excited state with exceptionally long lifetime (18.0 μs) and high molar absorptivity (29781 ± 180 M−1cm−1 at λmax 315 nm). The light-induced production of ROS promptly induced an unquenchable apoptotic process selectively in tumor cells, with mitoch…

Pharmaceutical ScienceApoptosisMitochondrionPhotochemiotherapy; Photosensitizing agents; Reactive oxygen species; [123]Triazolo[45-h][16]naphthyridines; [13]oxazolo[54-h][16]naphthyridines; Pharmacology; Drug Discovery; Pharmaceutical Science; Organic Chemistry01 natural sciencesMedicinal chemistry[13]oxazolo[54-h][16]naphthyridinechemistry.chemical_compoundDrug Discovery6]naphthyridineschemistry.chemical_classification0303 health sciencesTumorPhotosensitizing AgentsCell DeathSinglet OxygenSinglet oxygenPhotochemiotherapy; Photosensitizing agents; Reactive oxygen species; [1; 2; 3]Triazolo[4; 5-h][1; 6]naphthyridines; [1; 3]oxazolo[5; 4-h][1; 6]naphthyridines; Apoptosis; Cell Death; Cell Line; Tumor; Humans; Lysosomes; Mitochondria; Naphthyridines; Photochemotherapy; Photosensitizing Agents; Reactive Oxygen Species; Singlet OxygenGeneral MedicineLysosomeMitochondriaExcited stateReactive oxygen specie5-h][1HumanProgrammed cell death2NaphthyridinePhotochemiotherapy3]Triazolo[4Cell Line03 medical and health sciences4-h][1Cell Line TumorHumansNaphthyridines030304 developmental biologyPharmacologyReactive oxygen speciesPhotosensitizing agent010405 organic chemistryOrganic ChemistryApoptosi0104 chemical sciences3]oxazolo[5chemistryPhotochemotherapyCell cultureApoptosis[123]Triazolo[45-h][16]naphthyridine[1LysosomesReactive Oxygen SpeciesDerivative (chemistry)
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Recombinant water-soluble chlorophyll protein from Brassica oleracea var. Botrys binds various chlorophyll derivatives.

2003

A gene coding for water-soluble chlorophyll-binding protein (WSCP) from Brassica oleracea var. Botrys has been used to express the protein, extended by a hexahistidyl tag, in Escherichia coli. The protein has been refolded in vitro to study its pigment binding behavior. Recombinant WSCP was found to bind two chlorophylls (Chls) per tetrameric protein complex but no carotenoids in accordance with previous observations with the native protein [Satoh, H., Nakayama, K., Okada, M. (1998) J. Biol. Chem. 273, 30568-30575]. WSCP binds Chl a, Chl b, bacteriochlorophyll a, and the Zn derivative of Chl a but not pheophytin a, indicating that the central metal ion in Chl is essential for binding. WSCP …

PheophytinChlorophyllProtein FoldingDNA PlantLightTetrameric proteinPhotochemistryPigment bindingPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesProtoporphyrinsmacromolecular substancesBrassicaBiologyBiochemistrychemistry.chemical_compoundPigmentPhytolpolycyclic compoundsChlorophyll bindingChlorophyllidesSinglet OxygenCircular DichroismElectron Spin Resonance Spectroscopyfood and beveragesWaterCarotenoidsRecombinant ProteinsBiochemistrychemistrySolubilitySpectrophotometryChlorophyllvisual_artvisual_art.visual_art_mediumProtein foldingSpin LabelsOxidation-ReductionBiochemistry
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Facile synthesis of L-cysteine functionalized graphene quantum dots as a bioimaging and photosensitive agent

2021

Nowadays, a larger number of aggressive and corrosive chemical reagents as well as toxic solvents are used to achieve structural modification and cleaning of the final products. These lead to the production of residual, waste chemicals, which are often reactive, cancerogenic, and toxic to the environment. This study shows a new approach to the modification of graphene quantum dots (GQDs) using gamma irradiation where the usage of reagents was avoided. We achieved the incorporation of S and N atoms in the GQD structure by selecting an aqueous solution of L-cysteine as an irradiation medium. GQDs were exposed to gamma-irradiation at doses of 25, 50 and 200 kGy. After irradiation, the optical,…

PhotoluminescenceGeneral Chemical EngineeringQuantum yield02 engineering and technology010402 general chemistryPhotochemistrySettore FIS/07 - FISICA APPLICATA (A BENI CULTURALI AMBIENTALI BIOLOGIA E MEDICINA)01 natural sciencesArticlelaw.inventionchemistry.chemical_compoundlawGeneral Materials ScienceIrradiationbioimagingQD1-999Aqueous solutionatomic force microscopygraphene quantum dotsSinglet oxygenGraphene021001 nanoscience & nanotechnologygamma irradiation0104 chemical sciencesChemistrychemistryphotodynamic therapyQuantum dotReagentphotoluminescence0210 nano-technology
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Modification of Structural and Luminescence Properties of Graphene Quantum Dots by Gamma Irradiation and Their Application in a Photodynamic Therapy

2015

Herein, the ability of gamma irradiation to enhance the photoluminescence properties of graphene quantum dots (GQDs) was investigated. Different doses of gamma-irradiation were used on GQDs to examine the way in which their structure and optical properties can be affected. The photoluminescence quantum yield was increased six times for the GQDs irradiated with high doses compared to the nonirradiated material. Both photoluminescence lifetime and values of optical band gap were increased with the dose of applied gamma irradiation. In addition, the exploitation of the gamma-irradiated GQDs as photosensitizers was examined by monitoring the production of singlet oxygen under UV illumination. T…

PhotoluminescenceMaterials scienceLuminescenceBand gapQuantum yieldgraphene quantum dot02 engineering and technology010402 general chemistryPhotochemistryMicroscopy Atomic Force01 natural scienceslaw.inventionchemistry.chemical_compoundlawQuantum DotsSpectroscopy Fourier Transform InfraredGeneral Materials ScienceIrradiationParticle SizePhotosensitizing Agentsgraphene quantum dotsSinglet OxygenGraphenebusiness.industrySinglet oxygenElectron Spin Resonance Spectroscopy021001 nanoscience & nanotechnologygamma irradiation0104 chemical scienceschemistryPhotochemotherapyphotodynamic therapyQuantum dotGamma Raysgamma irradiation; graphene quantum dots; photodynamic therapy; photoluminescence; quantum yieldOptoelectronicsGraphiteSpectrophotometry Ultravioletphotoluminescence0210 nano-technologyLuminescencebusinessquantum yield
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