Search results for " Ultraviolet"

showing 10 items of 337 documents

Chromatographic separation of chlorthalidone enantiomers using β-cyclodextrins as chiral additives

2000

Different beta-cyclodextrins have been tested as chiral additives in the mobile phase for the chromatographic analysis of chlorthalidone enantiomers in a C18 LiChrospher (125 x 4 mm I.D.) column. The effect on enantioresolution of different parameters was studied: composition of the mobile phase (percentage of organic solvent, type of buffer and pH), mobile phase flow-rate, and type and concentration of beta-cyclodextrin. A 25:75 mixture of methanol and 0.1 M phosphate buffer, pH 4, containing 2% triethylamine (v/v), and 12.5 mM beta-cyclodextrin, at a flow-rate of 0.8 ml/min, was found to be the best option for the resolution of chlorthalidone enantiomers. Under such conditions, linear cal…

Beta-Cyclodextrinschemistry.chemical_compoundSpectrophotometrymedicineHumansDiureticsTriethylaminechemistry.chemical_classificationDetection limitCyclodextrinsChromatographyCyclodextrinmedicine.diagnostic_testbeta-CyclodextrinsChlorthalidoneStereoisomerismGeneral ChemistrySolutionschemistrySolventsIndicators and ReagentsSpectrophotometry UltravioletChlorthalidoneMethanolEnantiomermedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
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Sedimentation properties of chitosomal chitin synthetase from the wild-type strain and the 'slime' variant of Neurospora crassa.

1989

Marked differences in the pattern of sedimentation of cellular structures were observed after isopycnic centrifugation of crude cell-free preparations from the Neurospora crassa wall-less 'slime' variant and mycelial wild-type strain. Kinetic studies of particle sedimentation showed that the various types of subcellular components, as revealed by turbidity, UV absorption, polypeptide patterns, and chitin synthetase activity determinations, sediment independently of one another. An important feature was the finding that chitin synthetase from 'slime' peaked at a median specific gravity of 1.1201 +/- 0.0036, whereas that from wild-type strain sedimented at a higher buoyant density (specific g…

BiophysicsCentrifugation IsopycnicBiochemistryNeurospora crassaCell wallchemistry.chemical_compoundChitinCentrifugation Density GradientMolecular BiologyPolyacrylamide gel electrophoresisSpecific GravityDifferential centrifugationChitin SynthaseOrganellesbiologyStrain (chemistry)Neurospora crassafungiCrassaGenetic VariationSedimentationbiology.organism_classificationcarbohydrates (lipids)Molecular WeightKineticsMicroscopy ElectronNeurosporaBiochemistrychemistryGlucosyltransferasesElectrophoresis Polyacrylamide GelSpectrophotometry UltravioletBiochimica et biophysica acta
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In-vitro test system for the evaluation of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) inhibitors based on a single HPLC run with UV detect…

2001

Objective and Design: The aim of this study was to develop a new, whole-cell test system which is easy to handle and requires a standard equipment for the parallel screening of COX-1 and COX-2 inhibitors.¶Materials: Bovine aortic endothelial cells (BAECs).¶Treatment and methods: Unstimulated bovine aortic coronary endothelial cells (BAECs) were used as a source of COX-1 and BAECs pretreated with ASA (100 μM) and activated with phorbol myristate acetate (PMA) were used as a source of COX-2. The time- and concentration-dependent induction of COX-2 expression in the BAECs was evaluated by a kinetic profile (HPLC analysis) and detected by Western-Blot analysis using polyclonal antibodies agains…

Blotting WesternImmunologyDrug Evaluation PreclinicalAorta ThoracicIn Vitro TechniquesHigh-performance liquid chromatographyLipoxygenaseDiclofenacmedicineAnimalsCyclooxygenase InhibitorsLipoxygenase InhibitorsIC50Chromatography High Pressure LiquidPharmacologyCyclooxygenase 2 InhibitorsbiologyChemistryMolecular biologyIsoenzymesKineticsMeloxicamBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesPolyclonal antibodiesCyclooxygenase 1biology.proteinTetradecanoylphorbol AcetateAceclofenacCattleSpectrophotometry UltravioletEndothelium VascularCyclooxygenasemedicine.drugInflammation Research
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UV-PHOTOMETRY WITH THE 1.2 M SCHMIDT TELESCOPE IN BALDONE

2016

TheUniversityofLatvia's Institute of astronomy possesses a collection of 22 thousand photographic plates taken by the1.2 mSchmidt telescope located at the Baldone observatory. Among others, there are 767 astronegatives in this collection obtained in 314 sky areas using the Johnson U-filter. The field of view of each negative covers 19 square degrees. The plate scale is 72”/mm. The digitizing of the UV-collection has started in June 2016 with EPSON EXPRESSION 10000XL flatbed scanner. The general aim of the digitizing is to obtain UV-magnitudes and positions of all objects registered on the plates. Up to date near a half of the UV-collection is digitized. 24 digitized MEGA program plates of t…

Brightnesslcsh:Astronomymedia_common.quotation_subjectAstronomyField of viewSchmidt cameralaw.inventionPhotometry (optics)Telescopelcsh:QB1-991Starsdigital image processing; ultraviolet; star cataloguesSkylawObservatoryGeologymedia_commonOdessa Astronomical Publications
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Combination of ozonation and photocatalysis for purification of aqueous effluents containing formic acid as probe pollutant and bromide ion

2014

The treatment by advanced oxidation processes (AOPs) of waters contaminated by organic pollutants and containing also innocuous bromide ions may generate bromate ions as a co-product. In the present work heterogeneous photocatalysis and ozonation have individually been applied and in combination (integrated process) to degrade the organic compounds in water containing also bromide anions. The results show that: i) the sole photocatalysis does not produce bromate ions and in the case of its presence, it is able to reduce bromate to innocuous bromide ions; ii) the integration of photocatalysis and ozonation synergistically enhances the oxidation capabilities; and iii) in the integrated proces…

BromidesTime FactorsEnvironmental EngineeringFormatesTime FactorAdvanced oxidation processes; Bromate; Ozonation; Photocatalysis; Photocatalytic ozonation; Water purification; Bromates; Bromides; Catalysis; Formates; Ions; Kinetics; Oxidation-Reduction; Ozone; Time Factors; Water Pollutants Chemical; Ultraviolet Rays; Waste Disposal Fluid; Water Purification; Water Science and Technology; Waste Management and Disposal; Pollution; Ecological ModelingUltraviolet RaysFormic acidInorganic chemistryPortable water purificationWaste Disposal FluidCatalysisCatalysiCatalysischemistry.chemical_compoundOzonePhotocatalysiBromideOzonationIonWaste Management and DisposalBromateWater Science and TechnologyCivil and Structural EngineeringIonsKineticPhotocatalytic ozonationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionWater purificationBromatesEcological ModelingFormateBromatePollutionKineticschemistryUltraviolet RayBromidePhotocatalysisOxidation-ReductionWater Pollutants ChemicalAdvanced oxidation processeWaste disposalWater Research
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Laser-induced plasma spectroscopy in near vacuum ultraviolet using ordinary spectrograph and ICCD

2002

An experimental setup to measure laser-induced plasma emission spectra with an ordinary Czerny-Turner spectrograph and intensified charge-coupled device in the near vacuum ultraviolet down to 130 nm is described. Spectra of bromine, chlorine and iodine were recorded to demonstrate the performance of the setup.

BromineMaterials sciencebusiness.industrychemistry.chemical_elementAstrophysics::Cosmology and Extragalactic AstrophysicsPlasmaLaserSpectral linelaw.inventionVacuum ultravioletOpticschemistrylawLaser-induced breakdown spectroscopyEmission spectrumbusinessSpectrographAstrophysics::Galaxy AstrophysicsLaser Induced Plasma Spectroscopy and Applications
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Comparison of the performance of butanol and pentanol as modifiers in the micellar chromatographic determination of some phenethylamines

2000

Abstract A procedure was developed for the determination of several phenethylamines (amphetamine, arterenol, ephedrine, phenylephrine, phenylpropanolamine, mephentermine, methoxyphenamine, pseudoephedrine and tyramine), using micellar mobile phases of sodium dodecyl sulfate (SDS), a C18 column and UV detection. The drugs were eluted at short retention times with conventional acetonitrile–water or methanol–water mobile phases. In contrast, in the micellar system, they were strongly retained due to association with the surfactant adsorbed on the stationary phase, and needed the addition of butanol or pentanol to be eluted from the column. These modifiers allowed a simple way of controlling th…

ButanolsPhenethylaminesSensitivity and SpecificityBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundPentanolsPhenethylaminesmedicineEphedrineChromatography High Pressure LiquidMicellesChromatographyMethoxyphenamineElutionButanolOrganic ChemistryReproducibility of ResultsGeneral MedicinePseudoephedrinePharmaceutical PreparationschemistryIndicators and ReagentsSpectrophotometry UltravioletPhenylpropanolaminemedicine.drugJournal of Chromatography A
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Sulfated Lupane Triterpene Derivatives and a Flavone C-Glycoside from Gypsophila repens

2007

A new sulfated lupane triterpene, Gypsophilin (1), and its glucosyl ester, Gypsophilinoside (2) were isolated from the roots of Gypsophila repens whereas a new flavone C-glycoside (3) was obtained from the aerial parts. Their structures were established as (3beta)-3-O-(sulfo)lup-20(29)-en-23,28-dioic acid (1), (3beta)-3-O-(sulfo)lup-20(29)-en-23,28-dioic acid -28-O-beta-D-glucopyranosyl ester (2) and luteolin-7-O-alpha-L-arabinopyranosyl-6-C-beta-glucopyranoside (3) by spectroscopic methods such as 1D and 2D NMR, HR-ESI-MS and FAB-MS.

C glycosidesSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopySpectrophotometry InfraredStereochemistrySaponinCaryophyllaceaeCaryophyllaceaeSpectrometry Mass Fast Atom BombardmentSulfuric Acid EstersPlant RootsTerpeneSulfationTriterpeneDrug DiscoveryGlycosidesGypsophilinosidechemistry.chemical_classificationbiologyPlant ExtractsChemistryHydrolysisGypsophila repensGeneral ChemistryGeneral MedicineSaponinsbiology.organism_classificationTriterpenesSpectrophotometry UltravioletTwo-dimensional nuclear magnetic resonance spectroscopyGypsophilinChemical and Pharmaceutical Bulletin
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Photoreduction of carbon dioxide to formic acid in aqueous suspension: a comparison between phthalocyanine/TiO2 and porphyrin/TiO2 catalysed processes

2014

Composite materials prepared by loading polycrystalline TiO2 powders with lipophilic highly branched Cu(II)- and metal-free phthalocyanines or porphyrins, which have been used in the past as photocatalysts for photodegradative processes, have been successfully tested for the efficient photoreduction of carbon dioxide in aqueous suspension affording significant amounts of formic acid. The results indicated that the presence of the sensitizers is beneficial for the photoactivity, confirming the important role of Cu(II) co-ordinated in the middle of the macrocycles. A comparison between Cu(II) phthalocyanines and Cu(II) porphyrins indicated that the Cu(II)- phthalocyanine sensitizer was more e…

CO<sub>2</sub>IndolesPorphyrinsFormatesFormic acidPharmaceutical Sciencechemistry.chemical_elementIsoindolesphthalocyaninesPhotochemistryCatalysisArticleGas Chromatography-Mass SpectrometryAnalytical ChemistryCatalysisCatalysilcsh:QD241-441Porphyrinchemistry.chemical_compoundPhotochemical Processelcsh:Organic chemistryDrug Discoveryphoto-reductionTiO2Physical and Theoretical ChemistryTitaniumOrganic ChemistryWaterphthalocyanines/porphyrinsCarbon DioxideHydrogen-Ion ConcentrationPhotochemical ProcessesFormateAqueous suspensionPorphyrinheterogeneous photocatalysischemistryChemistry (miscellaneous)IndoleCarbon dioxidePhthalocyanineMolecular MedicineCO2Spectrophotometry UltravioletCrystalliteTiO<sub>2</sub>Oxidation-ReductionTitanium
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Electrodeless HF-lamps as UV and VUV light sources

2002

The paper is devoted to problems of employment of high- frequency electrodeless lamps as ultra violet (UV) and vacuum ultra violet (VUV) light sources. Some aspects of lamp preparation technology for UV and VUV are considered. The technology, developed in our laboratory, allows to prepare HFEL-s filled with wide spread of chemical elements. Our experience shows that most important filling elements for UV and VUV spectral regions are Zn, Cd, Hg, Se, As, Sn and Pb, Sb, Bi, Tl, Te, I, H, Hg-Cd, Hg-Zn, Se-Te. The requirements for generators are discussed. Some important spectral characteristics of lamp examples are presented.

Cadmiumbusiness.industryAnalytical chemistrychemistry.chemical_elementUltra violetZincHafniumMercury (element)Vacuum ultravioletchemistryOptoelectronicsbusinessTelluriumSeleniumSPIE Proceedings
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