Search results for "Spectrophotometry"

showing 10 items of 644 documents

Exposure to increased ambient ultraviolet B radiation has negative effects on growth, condition and immune function of juvenile Atlantic salmon (Salm…

2008

Atlantic salmon (Salmo salar) parr were exposed in two outdoor experiments, ranging in duration from 52 to 137 days, to spectral treatments: (1) natural sunlight (=present ambient UVB level), (2) solar radiation supplemented with enhanced UVB radiation from lamps simulating 20% or 8% stratospheric ozone loss or (3) UVB-depleted sunlight achieved by screening with Mylar-D film. The growth, condition and immune function of the salmon were quantified after treatments. Exposure to enhanced UVB radiation retarded growth, and decreased hematocrit value and plasma protein concentration. Further, enhanced UVB radiation affected plasma immunoglobulin concentration. The results demonstrate that juven…

Ultraviolet Raysanimal diseasesSalmo salarImmunoglobulinsBiologyHematocritBiochemistryAnimal scienceImmune systemRetarded growthmedicineJuvenileAnimalsPhysical and Theoretical ChemistrySalmoskin and connective tissue diseasesGrowth DisordersSunlightintegumentary systemmedicine.diagnostic_testEcologyGeneral Medicinebiology.organism_classificationBlood proteinsUltraviolet B radiationHematocritSpectrophotometry UltravioletPhotochemistry and photobiology
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Calcium-dependent conformational changes of membrane-bound Ebola fusion peptide drive vesicle fusion

2003

AbstractThe fusogenic subdomain of the Ebola virus envelope glycoprotein is an internal sequence located ca. 20 residues downstream the N-terminus of the glycoprotein transmembrane subunit. Partitioning of the Ebola fusion peptide into membranes containing phosphatidylinositol in the absence of Ca2+ stabilizes an α-helical conformation, and gives rise to vesicle efflux but not vesicle fusion. In the presence of millimolar Ca2+ the membrane-bound peptide adopts an extended β-structure, and induces inter-vesicle mixing of lipids. The peptide conformational polymorphism may be related to the flexibility of the virus–cell intermembrane fusogenic complex.

Vesicle fusionEbola glycoproteinSpectrophotometry InfraredProtein ConformationvirusesBiophysicsPeptideBiologymedicine.disease_causePhosphatidylinositolsBiochemistryMembrane FusionProtein Structure Secondarychemistry.chemical_compoundProtein structureFusion peptideMembranes (Biologia)Structural BiologyGeneticsmedicinePhosphatidylinositolMolecular Biologychemistry.chemical_classificationEbola virusVesicleCircular DichroismLipid bilayer fusionViral fusionWaterMembranes ArtificialCell BiologyEbolavirusLipidsTransmembrane proteinPeptide FragmentsBiochemistrychemistryLiposomesBiophysicsCalciumPèptidsPeptide–lipid interactionViral Fusion Proteins
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The lineshape of the electronic spectrum of the green fluorescent protein chromophore, part I: gas phase.

2014

The vibronic spectra of the green fluorescent protein chromophore analogues p-hydroxybenzylidene-2,3-dimethylimidazolinone (HBDI) and 3,5-tert-butyl-HBDI (35Bu) are similar in the vacuum, but very different in water or ethanol. To understand this difference, we have computed the vibrationally resolved solution spectra of these chromophores, using the polarizable continuum model (PCM) to account for solvent effects on the (harmonic) potential energy surfaces (PES). In agreement with experiment, we found that the vibrational progression increases with the polarity of the solvent, but we could neither reproduce the broadening, nor the large difference between the absorption spectra of HBDI and…

Vibrational spectroscopyComputational chemistrygenetic structuresAbsorption spectroscopySpectrophotometry InfraredPopulationGreen Fluorescent ProteinsAnalytical chemistryElectronsPolarizable continuum modelMolecular physicsAbsorptionMolecular dynamicsBenzyl CompoundsVibronic spectroscopyGreen fluorescent proteinPhysical and Theoretical ChemistryeducationImidazolinesta116education.field_of_studyChemistryTemperatureChromophoreChromophoresPotential energyAtomic and Molecular Physics and OpticsQuantum TheoryThermodynamicsGasesSolvent effectsChemphyschem : a European journal of chemical physics and physical chemistry
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Determination of ascorbic acid in plasma and urine by high performance liquid chromatography with ultraviolet detection.

1999

Abstract A reliable simple reversed-phase liquid chromatographic method for the routine determination of ascorbic acid in plasma and urine with ultraviolet detection is described. This method enables the complete separation of the ascorbic acid peak from others with a recovery of above 95 % within 8 minutes. The method can be used for analysing multiple samples within a day. In addition, the storage conditions and stability of ascorbic acid in plasma and urine were investigated. Samples of plasma and urine can be stored on ice in darkness for at least 60 min without reduction of ascorbic acid concentration. Prepared samples can be stored in darkness at 4 °C for at least 120 min and in liqui…

VitaminChromatographymedicine.diagnostic_testBiochemistry (medical)Clinical BiochemistryGeneral MedicineUrineReversed-phase chromatographyAscorbic AcidLiquid nitrogenAscorbic acidHigh-performance liquid chromatographySensitivity and Specificitychemistry.chemical_compoundchemistrySpectrophotometrymedicineHumansSpectrophotometry UltravioletQuantitative analysis (chemistry)Chromatography High Pressure LiquidClinical chemistry and laboratory medicine
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Spectrophotometric determination of vitamin C using the copper(II)-nioxime-ascorbic acid system following stabilization in a propylene glycol medium

1989

Abstract A spectrophotometric method for the determination of Vitamin C is proposed. The procedure is based on formation and stabilization of the ternary complex Cu(II)-nioxime-ascorbic acid in 80% ( v v ) propylene glycol-water medium. The method has a high degree of tolerance for the determination of ascorbic acid in the presence of other active substances or excipients likely to be present along with vitamin C in pharmaceutical formulations. The suggested method has proved to be rapid and precise and has been successfully applied to different commercial pharmaceutical preparations of vitamin C. Precision, measured on the relative standard deviation, did not exceed 0.73%.

VitaminChromatographymedicine.diagnostic_testVitamin Cchemistry.chemical_elementAscorbic acidPolyvinyl alcoholCopperAnalytical ChemistryPropanediolchemistry.chemical_compoundchemistrySpectrophotometrymedicineOrganic chemistryTernary complexSpectroscopyMicrochemical Journal
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Protein dynamics: conformational disorder, vibrational coupling and anharmonicity in deoxy-hemoglobin and myoglobin.

1993

In this work we study the temperature dependence of the Soret band lineshape of deoxymyoglobin and deoxyhemoglobin, in the range 300-20 K. To fit the measured spectra we use an approach originally proposed by Champion and coworkers (Srajer et al. 1986; Srajer and Champion 1991). The band profile is modelled as a Voigt function that accounts for the coupling with low frequency vibrational modes, whereas the coupling with high frequency modes is responsible for the vibronic structure of the spectra. Moreover, owing to the position of the iron atom out of the mean heme plane, inhomogeneous broadening brings about a non-Gaussian distribution of 0-0 electronic transition frequencies. The reporte…

Voigt profileChemical PhenomenaChemistry PhysicalMyoglobinProtein ConformationProtein dynamicsAnharmonicityBiophysicsTemperatureDynamic properties Heme proteins Optical spectroscopyGeneral MedicineMolecular physicsMolecular electronic transitionSpectral linechemistry.chemical_compoundHemoglobinsNuclear magnetic resonanceMyoglobinchemistrySpectrophotometryMolecular vibrationAnimalsThermodynamicsRotational–vibrational couplingEuropean biophysics journal : EBJ
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Dynamic properties of some β-chain mutant hemoglobins

1995

The thermal behavior of the Soret band relative to the carbonmonoxy derivatives of some beta-chain mutant hemoglobins is studied in the temperature range 300-10 K and compared to that of wild-type carbonmonoxy hemoglobin. The band profile at various temperatures is modeled as a Voigt function that accounts for homogeneous broadening and for the coupling with high- and low-frequency vibrational modes, while inhomogeneous broadening is taken into account with a gaussian distribution of purely electronic transition frequencies. The various contributions to the over-all bandwidth are singled out with this analysis and their temperature dependence, in turn, gives information on structural and dy…

Voigt profileCoupling constantBase SequenceChemistryProtein dynamicsMolecular Sequence DataAnharmonicityHemoglobin AHemeBiochemistryRecombinant ProteinsMolecular electronic transitionCold TemperatureCrystallographyCarboxyhemoglobinModels ChemicalSpectrophotometryStructural BiologyMolecular vibrationMutationMutagenesis Site-DirectedHomogeneous broadeningRotational–vibrational couplingMolecular BiologyProteins: Structure, Function, and Genetics
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Structure-dynamics-function relationships in Asian elephant (Elephas maximus) myoglobin. An optical spectroscopy and flash photolysis study on functi…

1993

In this work we report the thermal behavior (10–300 K) of the Soret band lineshape of deoxy and carbonmonoxy derivatives of Asian elephant (Elephas maximus) and horse myoglobins together with their carbon monoxide recombination kinetics after flash photolysis; the results are compared to analogous data relative to sperm whale myoglobin. The Soret band profile is modeled as a Voigt function that accounts for the coupling with high and low frequency vibrational modes, while inhomogeneous broadening is taken into account with suitable distributions of purely electronic transition frequencies. This analysis makes it possible to isolate the various contributions to the overall lineshape that; in…

Voigt profilePhotolysisMyoglobinProtein ConformationPhotodissociationElephantsAnalytical chemistryElectron Spin Resonance SpectroscopyBiophysicsSoft modesMolecular electronic transitionchemistry.chemical_compoundStructure-Activity RelationshipMyoglobinchemistryCarboxyhemoglobinChemical physicsSpectrophotometryMolecular vibrationFlash photolysisAnimalsThermodynamicsHorsesSpectroscopyResearch ArticleBiophysical Journal
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Retention pharmacokinetic and pharmacodynamic parameter relationships of antihistamine drugs using biopartitioning micellar chromatography

2001

Abstract Antihistamines are drugs which act by competitive inhibition of the H1 or H2 histamine receptors. Little has been known about their clinical pharmacokinetics and biological responses until the last few years. In this paper, we propose quantitative retention–activity relationship, QRAR, models based on the retention data of antihistamines in a biopartitioning micellar chromatography (BMC) system using a Brij35 mobile phase for describing pharmacokinetic parameters such as half-life and volume of distribution, or the pharmacodynamic parameters, therapeutic plasma levels, lethal doses and drug-receptor dissociation constant. The predictive ability of these models is statistically vali…

Volume of distributionQuantitative structure–activity relationshipChromatographyChemistrymedicine.medical_treatmentQuantitative Structure-Activity RelationshipGeneral ChemistryHigh-performance liquid chromatographyDissociation constantPharmacokineticsPharmacodynamicsLipophilicityHistamine H1 AntagonistsmedicineSpectrophotometry UltravioletAntihistamineChromatography LiquidJournal of Chromatography B: Biomedical Sciences and Applications
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Determination of total and free sulphur dioxide in wine with a continuous-flow microdistillation system

1993

Abstract A continuous-flow microdistillation system for the determination of SO2 (free and total) in wine samples is described. The assembly permits the successive addition of discrete volumes of sample to the microdistillation module with the aid of a nitrogen carrier stream. The nitrogen carrier also transports the volatilized SO2, after the distillation step, to the absorption module, where the analyte reacts with a solution of 2,2′-dinitro-5,5′-dithiodibenzoic acid in phosphate buffer (pH 6) to give a yellow derivative, which is monitored spectrophotometrically at 410 nm. Free and total so2 signals are obtained by operating the microdistillation module at room temperature (ca. 20°C) and…

WineAnalyteChromatographymedicine.diagnostic_testAnalytical chemistrychemistry.chemical_elementDerivativeBiochemistryNitrogenAnalytical Chemistrylaw.inventionchemistry.chemical_compoundHydrolysischemistrylawSpectrophotometrymedicineEnvironmental ChemistryDistillationSpectroscopySulfur dioxideAnalytica Chimica Acta
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