Search results for "Fluorometry"

showing 10 items of 30 documents

Nicotinic drugs and postganglionic sympathetic transmission

1970

1. Isolated rabbit hearts with the sympathetic nerves attached were perfused with Tyrode solution. The noradrenaline output into the perfusate was measured fluorimetrioally. 2. When the niootinic autoinhibition produced by infusions of nicotine, DMPP, or acetylcholine (in the presence of atropine) was fully developed, the output of noradrenaline evoked by electrical stimulation of the postganglionic sympathetic nerves was not depressed. 3. Acetylcholine in the presence of atropine produced a transitory facilitation of the noradrenaline output evoked by sympathetic nerve stimulation. 4. Prolonged infusion of DMPP caused an adrenergic neurone block which was not observed after nicotine, or ac…

MaleNicotinemedicine.medical_specialtySympathetic nervous systemSympathetic Nervous SystemReceptors DrugAdrenergicStimulationIn Vitro TechniquesSynaptic TransmissionPiperazinesNicotineNorepinephrineNorepinephrineInternal medicinemedicineAnimalsFluorometryGanglia AutonomicNerve EndingsPharmacologyChemistryHeartGeneral MedicineAcetylcholineElectric StimulationPerfusionAtropineEndocrinologyNicotinic agonistmedicine.anatomical_structureDepression ChemicalFemaleRabbitsAcetylcholinemedicine.drugNaunyn-Schmiedebergs Archiv f�r Pharmakologie
researchProduct

Noradrenaline depleting and blood pressure lowering activity of threo-corbadrine

1968

Abstract Threo-corbadrine caused a long-lasting depletion of noradrenaline in the heart and in mesenteric vessels and lowered the blood pressure of normal and renal hypertensive rats. It is suggested that threo-cobadrine decreases vascular tone by acting peripherally as a substitute adrenergic transmitter.

MalePharmacologymedicine.medical_specialtyHypertension RenalChromatography PaperChemistryInjections SubcutaneousAdrenergicBlood PressureMethylationRatsVascular tonePlethysmographyNorepinephrineEndocrinologyBlood pressureEthanolaminesLevonordefrinInternal medicinemedicineAnimalsPlethysmographFluorometryBlood pressure loweringEuropean Journal of Pharmacology
researchProduct

Metabolism of reduced pyridine nucleotides in ascites cell nuclei

1964

1. The conditions are described under which the fluorescence due to reduced pyridine nucleotides can be studied separately at nuclear and cytoplasmic sites of glass-grown ascites cells, by the use of a flow chamber in the microfluorimeter ofChance andLegallais.

NiacinamideHistologyNiacinFluorescenceFluorescence spectroscopyTissue Culture Techniqueschemistry.chemical_compoundPyridinemedicineFluorometryMicroscopy InterferenceNucleotideCitratesMolecular BiologyCell NucleusPharmacologychemistry.chemical_classificationMicroscopyNicotinamideHistocytochemistryNucleotidesResearchAscitesSuccinatesCell BiologyMetabolismNADMedical Laboratory TechnologyCell nucleusGlucoseMetabolismmedicine.anatomical_structureBiochemistrychemistryCytoplasmAmobarbitalNAD+ kinaseNADPHistochemie
researchProduct

Fluorescence-based assays for screening nine cytochrome P450 (P450) activities in intact cells expressing individual human P450 enzymes.

2004

In this study we describe a battery of fluorescence assays for rapid measurement in intact cells of the activity of nine cytochromes P450 (P450s) involved in drug metabolism. The assays are based on the direct incubation of monolayers of cells expressing individual P450 enzymes with a fluorogenic substrate followed by fluorimetric quantification of the product formed and released into incubation medium. For each individual P450 activity, different fluorescence probes were examined, and the one showing the best properties (highest metabolic rates, lowest background fluorescence) was selected: 3-cyano-7-ethoxycoumarin for CYP1A2 and CYP2C19, coumarin for CYP2A6, 7-ethoxy-4-trifluoromethylcoum…

Pharmacologychemistry.chemical_classificationTime FactorsbiologyEndoplasmic reticulumPharmaceutical ScienceCytochrome P450Molecular biologyIsozymeFluorescence spectroscopyIn vitroEnzymechemistryBiochemistryCytochrome P-450 Enzyme SystemMicrosomebiology.proteinHepatocytesMicrosomes LiverHumansFluorometryDrug metabolismCells CulturedFluorescent DyesDrug metabolism and disposition: the biological fate of chemicals
researchProduct

Pyrrolo[3,4-h]quinolinones a new class of photochemotherapeutic agents

2011

Abstract Pyrrolo[3,4- h ]quinolin-2-ones were synthesized as nitrogen isosters of the angular furocoumarin angelicin, with the aim of obtaining new photochemotherapeutic agents with increased antiproliferative activity and lower undesired toxic effects. A versatile synthetic pathway was approached to allow the isolation of derivatives of the new ring system with a good substitution pattern on the pyrrole moiety. Photobiological screenings of the new compounds revealed a potent phototoxic effect and a great UVA dose dependence, reaching IC 50 values at submicromolar level. The induced cellular photocytotoxicity was related to apoptosis with the involvement of mitochondria and lysosomes, alte…

Pyrrolo[3; 4-h]quinolinones; Angelicin heteroanalogues; Photochemotherapeutic agents; PhototoxicityStereochemistryClinical BiochemistryMembrane lipid peroxidationPharmaceutical ScienceHL-60 CellsPhosphatidylserinesQuinolonesMitochondrionBiochemistryPhototoxicityJurkat CellsStructure-Activity Relationshipchemistry.chemical_compoundPhotochemotherapeutic agentsAngelicinCell Line TumorDrug DiscoveryHumansMoietyFluorometryPyrrolesPyrrolo[3Molecular BiologyPyrrolePyrrolo[34-h]quinolinoneFurocoumarinCell CycleOrganic Chemistry4-h]quinolinonesDNAPhotochemical ProcessesSettore CHIM/08 - Chimica FarmaceuticaAngelicin heteroanaloguesPhotochemotherapeutic agentPhotochemotherapychemistryApoptosisMolecular MedicineLipid PeroxidationPhototoxicityAngelicin heteroanalogueSubcellular FractionsBioorganic & Medicinal Chemistry
researchProduct

Fit-for-purpose chromatographic method for the determination of amikacin in human plasma for the dosage control of patients

2015

In this paper, a simple, rapid and sensitive method based on liquid chromatography with fluorimetric detection (HPLC-FLD) for the determination of amikacin (AMK) in human plasma is developed. Determination is performed by pre-column derivatization of AMK with ortho-phtalaldehyde (OPA) in presence of N-acetyl-L-cysteine (NAC) at pH 9.5 for 5 min at 80 °C. In our knowledge, this is the first time that NAC has been used in AMK derivatization. Derivatization conditions (pH, AMK/OPA/NAC molar ratios, temperature and reaction time) are optimized to obtain a single and stable, at room temperature, derivative. Separation of the derivative is achieved on a reversed phase LC column (Kromasil C18, 5 μ…

Quality ControlCorrelation coefficientAnalytical chemistryDerivative01 natural sciencesFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundmedicineHumansFluorometryDerivatizationAcetonitrileAmikacinChromatography High Pressure LiquidChromatographyDose-Response Relationship DrugPlasma samples010405 organic chemistry010401 analytical chemistryBacterial InfectionsAnti-Bacterial Agents0104 chemical scienceschemistryHuman plasmaAmikacinSpectrophotometry Ultravioletmedicine.drug
researchProduct

Analysis of Urine Samples Containing Cardiovascular Drugs by Micellar Liquid Chromatography with Fluorimetric Detection

1999

A simple direct injection chromatographic procedure with fluorimetric detection is successfully applied to the determination of mixtures of 4 diuretics (amiloride, bendroflumethiazide, piretanide, and triamterene) and 6 beta-blockers (acebutolol, atenolol, labetalol, metoprolol, nadolol, and propranolol), which are usually administered in combinations for the treatment of hypertension, in urine samples. The procedure makes use of C18 columns and micellar mobile phases of sodium dodecyl sulphate (SDS), propanol, and phosphate buffer at pH 3. The adequate resolution of most drugs is obtained with a chemometrics approach where the retention is modeled as a first step using the retention factor…

Quality Controlmedicine.medical_treatmentAdrenergic beta-AntagonistsMicellar electrokinetic chromatographyAnalytical ChemistryPropanolSurface-Active Agentschemistry.chemical_compoundmedicineHumansFluorometryBendroflumethiazideDiureticsAntihypertensive AgentsMicellesTriamtereneChromatographyChemistryElutionPiretanideGeneral MedicineHydrogen-Ion ConcentrationMicellar liquid chromatographyIndicators and ReagentsDiureticMathematicsChromatography Liquidmedicine.drugJournal of Chromatographic Science
researchProduct

Application of DNA techniques for identification using human dental pulp as a source of DNA

1992

Dental pulp tissue could be obtained in most cases from materials obtained under experimental conditions and from forensic casework (air accidents, burned and putrefied bodies). Teeth extracted during dental treatment (n = 30) were stored for 6 weeks and 4 years at room temperature. In addition teeth (n = 10) extracted from jaw fragments that had been stored for 15 years at room temperature, and teeth extracted post mortem from actual identification cases (n = 8) were investigated. Following extraction from dental pulp tissue the DNA concentration was measured by fluorometry. The amount of DNA obtained from the dental pulp tissue of a single tooth varied from 6 micrograms to 50 micrograms D…

Sex Determination AnalysisImmunoblottingDot blotBiologyPolymerase Chain ReactionPathology and Forensic Medicinechemistry.chemical_compoundstomatognathic systemHumansFluorometryDental PulpSouthern blotHistocompatibility TestingDna concentrationSingle toothDNA FingerprintingMolecular biologyBlotBlotting Southernstomatognathic diseaseschemistryEvaluation Studies as TopicDegraded dnaHigh molecular weight dnaDNAForensic DentistryInternational Journal of Legal Medicine
researchProduct

FIA-fluorimetric determination of thiamine.

1990

A flow injection-fluorimetric determination of thiamine is reported. The procedure is based on the oxidation of the analyte with potassium hexacyanoferrate(III) immobilized on an anionic exchange resin; the fluorescence is monitored in aqueous basic solution. Concentrations of the vitamin of 0.1-4 ppm have been determined; the relative standard deviation was 1.8%. The injection rate was 28 samples/h. The influence of other substances and the determination of the drug in a pharmaceutical formulation are also reported.

VitaminAnalyteAqueous solutionChromatographyChemistryPotassiumClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementPharmaceutical formulationFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundBasic solutionDrug DiscoveryThiamineFluorometryIndicators and ReagentsThiamineOxidation-ReductionSpectroscopyResins PlantJournal of pharmaceutical and biomedical analysis
researchProduct

Diagnostic efficacy of the fluorometric determination of enzyme activity for Pompe disease from dried blood specimens compared with lymphocytes-possi…

2009

Pompe disease is a rare, autosomal-recessive disorder which results from a defect in the lysosomal enzyme acid alpha-glucosidase (GAA). The onset of this disease is highly variable, with infantile types being the most severe. Traditionally, lymphocytes, fibroblasts or muscle biopsies were necessary for enzyme activity measurement, because these materials do not express maltase-glucoamylase (MGA) that interferes with the assay. Recently, acarbose was found to inhibit MGA activity selectively, so that dried blood became accessible for GAA assessment.To evaluate the diagnostic efficacy of GAA measurement in dried blood specimens (DBSs) in comparison with lymphocytes. If DBSs provided reliable …

medicine.medical_specialtyTime FactorsLymphocyteBiopsyNeonatal ScreeningInternal medicineBiopsyGeneticsmedicineHumansFalse Positive ReactionsFluorometryLymphocytesGenetics (clinical)Acarbosechemistry.chemical_classificationNewborn screeningmedicine.diagnostic_testbiologybusiness.industryGlycogen Storage Disease Type IIMusclesInfant NewbornReproducibility of Resultsalpha-GlucosidasesEnzyme replacement therapyFibroblastsHydrogen-Ion ConcentrationEnzyme assaymedicine.anatomical_structureEndocrinologyEnzymechemistryCarbohydrate Metabolism Disorderbiology.proteinFeasibility Studiesbusinessmedicine.drugJournal of inherited metabolic disease
researchProduct