Search results for "photosensitizer"

showing 10 items of 44 documents

Novel meso-substituted porphyrins: Synthesis, characterization and photocatalytic activity of their TiO2-based composites

2009

Abstract Two series of novel meso-substituted porphyrins, namely 5,10,15,20-tetra[4-(3-phenoxy)-propoxy]phenyl porphyrin, the structural analogue 5,10,15,20-tetra[2-(3-phenoxy)-propoxy]phenyl porphyrin and their Co(II) Cu(II) and Zn(II) complexes were synthesized. The compounds were characterized using various spectroscopic techniques and their molecular structure was proposed based on density functional theory calculations. The diverse properties of the porphyrin derivatives result from the different stereochemistry of the particular substituents at the meso site on the macrocycle and are controlled also by the coordinated metal. The 1H NMR spectrum of the free-base porphyrin showed a comp…

PorphyrinsMetalloporphyrinsProcess Chemistry and TechnologyGeneral Chemical EngineeringPhotosensitizerDFT calculationsPhotochemistryPorphyrinMetalchemistry.chemical_compoundchemistryvisual_artPhotodegradationPolymer chemistryvisual_art.visual_art_mediumProton NMRPhotocatalysisTiO2MoleculePhotosensitizerDensity functional theoryPhotodegradationporphyrinphotocatalysisDyes and Pigments
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A novel pro-apoptotic role of zinc octacarboxyphthalocyanine in melanoma me45 cancer cell's photodynamic therapy (PDT)

2018

Abstract Zn-based phthalocyanine acts as drug or photosensitizer in photodynamic therapy (PDT) for the treatment of cancer cells. The activated zinc octacarboxyphthalocyanine (ZnPcOC) reacts with oxygen, to generate reactive oxygen species for the damage of melanoma cancer cells, Me45. This in vitro study aimed at investigating the cytotoxic effects of different concentrations of ZnPcOC activated with a diode laser (λ = 685 nm) on Me45, and normal human fibroblast cells, NHDF. To perform this study 104 cells/ml were seeded in 96-well plates and allowed to attach overnight, after which cells were treated with different concentrations of ZnPcOC (10, 20 and 30 μM). After 4 h, cells were irradi…

Programmed cell deathIndolesCell Survivalmedicine.medical_treatmentPhotodynamic therapy (PDT)030303 biophysicsBiophysicsApoptosisPhotodynamic therapy02 engineering and technologyIsoindolesZinc octacarboxyphthalocyanine (ZnPcOC)PhotosensitizersCell Line03 medical and health sciencesCell Line TumorOrganometallic CompoundsmedicineHumansCytotoxic T cellRadiology Nuclear Medicine and imagingPhotosensitizerViability assayMelanoma0303 health sciencesPhotosensitizing AgentsRadiationRadiological and Ultrasound TechnologyChemistryMelanomaReactive oxygen species (ROS)UV–Vis spectraFibroblasts021001 nanoscience & nanotechnologymedicine.diseasePhotochemotherapyZinc CompoundsApoptosisCancer cellCancer researchMelanoma Me45 cancer cellsLasers SemiconductorPro-apoptotic activityReactive Oxygen Species0210 nano-technologyJournal of Photochemistry and Photobiology B-Biology
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Oxidative DNA damage and mutations induced by a polar photosensitizer, Ro19-8022.

1999

The oxidative DNA damage induced by the polar photosensitizer Ro19-8022 in the presence of light was studied and correlated with the associated mutagenicity. Both in isolated DNA and AS52 Chinese hamster ovary cells, photoexcited Ro19-8022 gave rise to a DNA damage profile that was similar to that caused by singlet oxygen: base modifications sensitive to the repair endonuclease Fpg protein, which according to high-performance liquid chromatography (HPLC) analysis were predominantly 8-hydroxyguanine (8-oxoG) residues, were generated in much higher yield than single-strand breaks, sites of base loss (AP sites) and oxidative pyrimidine modifications sensitive to endonuclease III. Fifty percent…

PyrrolidinesDNA damageMolecular Sequence DataCHO CellsBiologyToxicologymedicine.disease_causechemistry.chemical_compoundPlasmidCricetinaeGeneticsmedicineAnimalsPhotosensitizerMutation frequencyMolecular BiologyGenePhotosensitizing AgentsBase SequenceCell-Free SystemChinese hamster ovary cellOxidative StressBiochemistrychemistryDNA ViralMutationDNAOxidative stressQuinolizinesDNA DamageMutation research
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Pyrrolo[2,3-h]quinolinones: synthesis and photochemotherapic activity.

2003

A series of derivatives of the new ring system pyrrolo[2,3-h]quinoline-2-one was synthesized and evaluated as photoreagents toward cultured human tumor cells. Remarkable phototoxycity resulted for some derivatives, especially those bearing the phenyl group at the 7-position.

StereochemistryFibrosarcomaClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsQuinolonesRing (chemistry)BiochemistryChemical synthesischemistry.chemical_compoundStructure-Activity RelationshipDrug DiscoveryTumor Cells CulturedPhenyl groupHumansPhotosensitizerPyrrolesMolecular BiologyPhotosensitizing AgentsChemistryOrganic ChemistryGeneral MedicineIn vitroHuman tumorPhotochemotherapyCell cultureLactamMolecular MedicineDrug Screening Assays AntitumorBioorganicmedicinal chemistry letters
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Hypoxia-Selective Dissociation Mechanism of a Nitroimidazole Nucleoside in a DNA Environment

2019

Photodynamic therapy is a promising approach to treat a variety of superficial tumors and other diseases. One of its major limitations arises from its dependence on molecular oxygen, which decreases the efficiency of the therapy in hypoxia conditions commonly developed by solid tumors. The present contribution reveals the molecular mechanism of a modified thymine bearing a nitroimidazole substituent, a photosensitizer able to produce highly harmful interstrand cross-links in the DNA double strand after irradiation selectively in absence of oxygen. The mechanism is resolved at a fully atomistic and electronic level relying on quantum mechanics (CASPT2, coupled-cluster, DFT, and TD-DFT method…

SubstituentMolecular Dynamics Simulation010402 general chemistry01 natural scienceschemistry.chemical_compoundMolecular dynamics[CHIM]Chemical SciencesGeneral Materials SciencePhotosensitizerA-DNAPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSPhotosensitizing AgentsNitroimidazole010405 organic chemistryHydrogen bondHydrogen BondingDNA0104 chemical sciencesThyminechemistryNitroimidazolesBiophysicsNucleic Acid ConformationQuantum TheoryDNAThe Journal of Physical Chemistry Letters
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Triggering the generation of an iron(IV)-oxo compound and its reactivity toward sulfides by RuII photocatalysis

2014

The preparation of [FeIV(O)(MePy2tacn)]2+ (2, MePy2tacn = N-methyl-N,N-bis(2-picolyl)-1,4,7-triazacyclononane) by reaction of [FeII(MePy2tacn)(solvent)]2+ (1) and PhIO in CH3CN and its full characterization are described. This compound can also be prepared photochemically from its iron(II) precursor by irradiation at 447 nm in the presence of catalytic amounts of [Ru II(bpy)3]2+ as photosensitizer and a sacrificial electron acceptor (Na2S2O8). Remarkably, the rate of the reaction of the photochemically prepared compound 2 toward sulfides increases 150-fold under irradiation, and 2 is partially regenerated after the sulfide has been consumed; hence, the process can be repeated several times.…

SulfideFotocatàlisi010402 general chemistryPhotochemistry01 natural sciencesBiochemistryChemical reactionArticleCatalysisCatalysisReaccions químiquesReaction rateColloid and Surface ChemistrySofre -- CompostosChemical reactionsSulphur compoundsOrganic chemistryWATER[CHIM.COOR]Chemical Sciences/Coordination chemistryPhotosensitizerReactivity (chemistry)Photocatalysischemistry.chemical_classificationOXYGENATION REACTIONS010405 organic chemistryChemistryGeneral ChemistryElectron acceptorSTATE0104 chemical sciencesELECTRON-TRANSFER PROPERTIESC-H OXIDATIONSPIN FE(IV) COMPLEXPhotocatalysisIRON-OXO COMPLEXESLIGANDTAURINE/ALPHA-KETOGLUTARATE DIOXYGENASENONHEME OXOIRON(IV) COMPLEXES
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Release of Inflammatory Mediators (PGE2, IL-6) by Fenofibric Acid-Photosensitized Human Keratinocytes and Fibroblasts

1998

Ultraviolet-A radiation has weak effects on the release of inflammatory mediators by skin cells due to the poor overlap between UVA wavelengths and the absorption spectra of the relevant chromophores of key biomole-cules. However, this situation could be very different in the presence of a photosensitizing drug. To investigate this issue, we have irradiated human skin cells (keratinocytes and fibroblasts) in the presence of fenofibric acid (the active phototoxic metabolite of fenofibrate). The results of this research show a dual effect on the production/release of inflammatory mediators: the synthesis of the proinflammatory cytokine interleukin-6 becomes strongly inhibited at photosensitiz…

biologyMetaboliteHuman skinStimulationGeneral MedicineBiochemistryMolecular biologyProinflammatory cytokinechemistry.chemical_compoundBiochemistrychemistryIn vivobiology.proteinPhotosensitizerPhysical and Theoretical ChemistryInterleukin 6PhototoxicityPhotochemistry and Photobiology
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EFFECTS OF SENSITIZED AND UNSENSITIZED LONGWAVE U.V.-IRRADIATION ON THE SOLUTION PROPERTIES OF DNA

1971

— Two types of photoreactions occur in DNA irradiated in aqueous systems with longwave u.v.-light (Λ > 295 nm), namely, (a) thymine dimerization, and (b) single- and double-strand breakage of the sugar phosphate backbone; these two reactions are unrelated. The presence of acetophenone as a photosensitizer caused an increase in dimerization by a factor of 16, and an increase in single-strand breaks by a factor of 4. The number of thymine dimers per single-strand break is about 100 in the sensitized and 25 in the unsensitized reaction. The alteration of the radius of gyration of DNA molecules is that expected by the degradation observed. At the same time the change in hyperchromicity is very …

chemistry.chemical_classificationCarbon IsotopesAqueous solutionSugar phosphatesUltraviolet RaysHyperchromicityPyrimidine dimerDNAGeneral MedicinePhotochemistryBiochemistryThymineRadiation Effectschemistry.chemical_compoundchemistryEscherichia coliRadius of gyrationPhotosensitizerPhysical and Theoretical ChemistryThymineDNAPhotochemistry and Photobiology
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Effect of phosphatydylcholine on spectral properties and photostability of 3,3′-diethyloxadicarbocyanine iodide (DODCI) — a potent anti-tumor photose…

1998

Abstract The potential anti-tumor photosensitizer 3,3′-diethyloxadicarbocyanine iodide (DODCI) has been immobilized in dimyristoyl phosphatidylcholine (DMPC) vesicles. Binding of the dicarbocyanine to the lipid vesicles induces several changes in the electronic absorption, emission and excitation spectra of the dye. The monomeric dye molecules exist in at least two forms when immobilized in the DMPC liposomes and the non-luminescing H-aggregates of the dye show efficient excitation energy transfer to the DODCI monomers. Entrapment of the dye in the liposomes generally decreases the photostability of DODCI. While emission from singlet oxygen (1O2) has not been recorded, indirect results sugg…

chemistry.chemical_classificationLiposomeSinglet oxygenVesicleOrganic ChemistryIodidetechnology industry and agriculturePhotochemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPhosphatidylcholinelipids (amino acids peptides and proteins)PhotosensitizerAbsorption (chemistry)SpectroscopyJournal of Molecular Structure
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Water-soluble hyperbranched polyglycerol photosensitizer for enhanced photodynamic therapy

2020

Porphyrin and its derivatives as promising photosensitizers have been widely utilized in photodynamic therapy (PDT). However, the water-solubility and biocompatibility of porphyrins are the typical bottlenecks in clinical PDT processes. Herein, we successfully fabricated a new type of water-soluble, hyperbranched polyglycerol photosensitizer through one-step esterification between water-soluble hyperbranched polyglycerol (hbPG) and fluorophenylporphyrin (FP). Compared with the linear control polymer, i.e., FP covalently connected with linear polyethylene glycol (LPEG), the hyperbranched structures bearing multiple porphyrin units generated more singlet oxygen and exhibited higher cytotoxici…

chemistry.chemical_classificationPolymers and PlasticsBiocompatibilitySinglet oxygenmedicine.medical_treatmentOrganic ChemistryBioengineeringPhotodynamic therapyPolymerBiochemistryCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryCovalent bondpolycyclic compoundsmedicinePhotosensitizerCytotoxicityPolymer Chemistry
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