Search results for "Indicators and Reagent"

showing 10 items of 145 documents

Fast enantiomeric separation of uniconazole and diniconazole by electrokinetic chromatography using an anionic cyclodextrin: application to the deter…

2000

The enantiomeric resolution of the fungicides uniconazole and diniconazole was performed using electrokinetic chromatography with cyclodextrins as pseudostationary phase (CD-EKC). A systematic evaluation of several chiral selectors was made. The anionic derivative carboxymethylated-gamma-cyclodextrin (CM-gamma-CD) was found to be the most appropriate for the enantioseparation of fungicides among all cyclodextrins tested. The influence of some experimental conditions such as nature and buffer pH, chiral selector concentration, and temperature on the enantiomeric separation of the compounds studied was also investigated. The use of a 50 mM phosphate buffer (pH 6.5) containing 5 mM CM-gamma-CD…

CienciaAnalyteResolution (mass spectrometry)Electrokinetic chromatographyScienceClinical BiochemistryUniconazoleChemistry analytic and technicalDerivativeBiochemistryAnalytical ChemistryElectrokinetic phenomenaPhase (matter)CIENCIAchemistry.chemical_classificationCyclodextrinsChromatographyCyclodextrinElectrophoresis CapillaryStereoisomerismQuímica analítica e industrialSCIENCETriazolesDiniconazoleFungicides IndustrialUniconazolechemistryIndicators and ReagentsEnantiomer
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Comparison of several methods used for the determination of cephalosporins. Analysis of cephalexin in pharmaceutical samples

2002

The precision of UV absorbance of intact and acid degraded cephalosporins, ninhydrin, high performance liquid chromatography and iodometric methods used for analysis of cefoxitin, cefotaxime, cephazolin and cephalexin were compared. To obtain the calibration graphs the analytical signal used were: absorbance, first derivative absorbance, second derivative absorbance and H-point Standard Additions Method by using absorbance values at two selected wavelengths as analytical signal. These methods and calibration graphs were also used for the determination of cephalexin in pharmaceutical samples.

Clinical BiochemistryPharmaceutical ScienceCapsulesHigh-performance liquid chromatographyAnalytical ChemistryAbsorbancechemistry.chemical_compoundIodometrySpectrophotometryDrug Discoverypolycyclic compoundsmedicineChromatography High Pressure LiquidSpectroscopyAntibacterial agentSecond derivativeCephalexinChromatographymedicine.diagnostic_testChemistrydigestive oral and skin physiologyTitrimetryNinhydrinCephalosporinsSolutionsStandard additionNinhydrinIndicators and ReagentsSpectrophotometry UltravioletJournal of Pharmaceutical and Biomedical Analysis
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Furosemide assay in pharmaceuticals by Micellar liquid chromatography: study of the stability of the drug.

2000

A simplified high-performance liquid chromatographic procedure is described for the determination of furosemide (4-chloro-N-furfuryl-5-sulphamoylanthranillic acid), which makes use of UV detection, a C18, reversed-phase column, and micellar mobile phases of sodium dodecyl sulphate (SDS) and 1-propanol at pH 3 buffered with phosphate system. The most adequate experimental conditions to handle furosemide solutions in the analytical laboratory are studied. The mixture of furosemide and its degradation products which are formed upon light exposition was resolved with a mobile phase of 0.04 M SDS-2% propanol. Separation of furosemide from its common impurities and the hydrolytic product, 4-chlor…

Clinical BiochemistryPharmaceutical ScienceDosage formMicellar electrokinetic chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundDrug StabilityFurosemideDrug DiscoverymedicineSodium dodecyl sulfateDiureticsSpectroscopyChromatography High Pressure LiquidMicellesChromatographyPhotolysisElutionHydrolysisFurosemideSodium Dodecyl SulfateHydrogen-Ion ConcentrationSolutionschemistryMicellar liquid chromatographyCalibrationIndicators and ReagentsSpectrophotometry UltravioletQuantitative analysis (chemistry)medicine.drugTabletsJournal of pharmaceutical and biomedical analysis
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Polydimethylsiloxane composites containing 1,2-naphtoquinone 4-sulphonate as unique dispositive for estimation of casein in effluents from dairy indu…

2015

A unique dispositive to determine casein which is the most abundant protein in dairy sewages has been proposed. In this sensing technology, the derivatization reagent 1,2-naphtoquininone 4-sulphonate (NQS) is embedded into a polydimethylsiloxane-tetraethylortosilicate-SiO2 nanoparticles composite (PDMS-TEOS-SiO2NPs). When the composite is immersed into the samples, casein is extracted from the solution and derivatized inside the PDMS matrix after 10 min at 100°C. The sensing support changes its color from yellow to orange depending on the casein concentration. Quantitative analysis can be carried out by measuring the absorbance with a reflection probe or by image-processing tool (GIMP). Thi…

Composite numberNQSNanoparticleWastewaterBiochemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundCaseinEnvironmental ChemistryAnimalsDimethylpolysiloxanesDerivatizationSpectroscopyChromatographyPolydimethylsiloxaneCaseinsSilicon DioxideDairyingchemistryReagentColorimetryIndicators and ReagentsSpectrophotometry UltravioletSulfonic AcidsNaphthoquinonesAnalytica chimica acta
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Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells

2005

AbstractCadherin 23 is required for normal development of the sensory hair bundle, and recent evidence suggests it is a component of the tip links, filamentous structures thought to gate the hair cells' mechano-electrical transducer channels. Antibodies against unique peptide epitopes were used to study the properties of cadherin 23 and its spatio-temporal expression patterns in developing cochlear hair cells. In the rat, intra- and extracellular domain epitopes are readily detected in the developing hair bundle between E18 and P5, and become progressively restricted to the distal tip of the hair bundle. From P13 onwards, these epitopes are no longer detected in hair bundles, but immunoreac…

CytoplasmTime FactorsStereocilia (inner ear)EpitopesMice0302 clinical medicineCDH23Inner earMicroscopy ImmunoelectronEgtazic AcidCells Cultured0303 health sciencesintegumentary systemReverse Transcriptase Polymerase Chain ReactionGene Expression Regulation DevelopmentalAnatomyCadherinsHair bundleImmunohistochemistryCochleaCell biologymedicine.anatomical_structureEctodomainHair cellHair cellTransduction (physiology)Signal TransductionMechano-electrical transductionDevelopmentBiologyStereocilia03 medical and health sciencesLanthanumCadherin 23Hair Cells Auditoryotorhinolaryngologic diseasesmedicineAnimalsMolecular BiologyTip link030304 developmental biologyModels GeneticCadherinSubtilisinCell BiologyProtein Structure TertiaryRatsMicroscopy ElectronMicroscopy FluorescenceEar InnerIndicators and Reagentssense organsTip linkLateral linksUsher type 1 syndrome030217 neurology & neurosurgeryPCDH15Developmental BiologyDevelopmental Biology
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Micellar electrokinetic chromatography with bile salts for predicting ecotoxicity of aromatic compounds.

2004

The retention factors of several aromatic compounds were obtained by micellar electrokinetic chromatography (MEKC) using cholate, taurocholate, deoxycholate and deoxytaurocholate as micellar systems. The possibility of using these retention factors to describe and predict several ecotoxicological activities of different aromatic compounds was evaluated. Adequate correlations retention–ecotoxicity (log LC50 in fish and daphnia, log EC50 in green algae and daphnia, chronic values in fish and green algae, bioconcentration factor, and soil sorption coefficient) were obtained for the micellar systems studied. The predictive ability of the models obtained for these micellar systems was compared. …

Daphnia magnaPolycyclic aromatic hydrocarbonBioconcentrationmacromolecular substancesBiochemistryDaphniaMicellar electrokinetic chromatographyAnalytical ChemistryBile Acids and SaltsAnimalsPolycyclic CompoundsChromatography Micellar Electrokinetic Capillarychemistry.chemical_classificationChromatographybiologyOrganic ChemistryFishesGeneral MedicineReference Standardsbiology.organism_classificationHydrocarbonchemistryDaphniaEnvironmental chemistryGreen algaeIndicators and ReagentsEcotoxicityWater Pollutants ChemicalJournal of chromatography. A
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Liquid Chromatographic Analysis of Amphetamine and Related Compounds in Urine Using Solid-Phase Extraction and 3,5-Dinitrobenzoyl Chloride for Deriva…

1997

A chromatographic method for the analysis of amphetamine and related compounds in urine using 3,5-dinitrobenzoyl chloride (3,5-DNB) as a labeling reagent is presented. This assay is based on the employment of solid-phase extraction (SPE) cartridges for sample cleanup and derivatization. Experimental conditions are optimized for the simultaneous derivatization of ephedrine, norephedrine, pseudoephedrine, beta-phenylethylamine, amphetamine, methamphetamine, and 3-phenylpropylamine. The derivatives formed are separated in a LiChrospher 1000 RP18 (125 x 4-mm i.d., 5-microns film thickness) analytical column using a water-acetonitrile gradient elution and detected at 254 nm. Derivatization in C1…

Detection limitAnalyteChromatographyAmphetaminesGeneral MedicinePseudoephedrineHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNitrobenzoatesReagentmedicineIndicators and ReagentsSolid phase extractionEphedrineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatographic Science
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High-performance liquid chromatographic determination of spironolactone and its major metabolite canrenone in urine using ultraviolet detection and c…

1994

A rapid and simple column liquid chromatographic method involving a column-switching system for the determination of spironolactone and its main metabolite canrenone in urine is described. Purification and concentration was performed using an Hypersil ODS-C18, 30 microns (20 x 2.1 mm I.D.) pre-column. The most polar urinary compounds were removed by washing the pre-column with water, and the analytes were subsequently switched to a LiChrospher RP C18, 5 microns (125 x 4 mm I.D.) analytical column and separated by means of an acetonitrile-water mobile-phase. Under the proposed conditions, the extraction efficiency was approximately 100% over the 0.5-10.0 micrograms/ml concentration range. Th…

Detection limitAnalyteChromatographyChemistryMetaboliteExtraction (chemistry)General ChemistryUrineSpironolactoneHigh-performance liquid chromatographychemistry.chemical_compoundCanrenonemedicineHumansIndicators and ReagentsSpectrophotometry UltravioletCanrenoneQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical applications
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Solid-Phase Microextraction Liquid Chromatography/Tandem Mass Spectrometry To Determine Postharvest Fungicides in Fruits

2003

A method to determine five postharvest fungicides (dichloran, flutriafol, o-phenylphenol, prochloraz, tolclofos methyl) in fruits (cherries, lemons, oranges, peaches) has been developed using solid-phase microextraction (SPME) coupled to liquid chromatography (LC) with photodiode array (DAD), mass spectrometry (MS), or tandem mass spectrometry (MS/MS) with ion trap detection. Extraction involved sample homogenization with an acetone/water solution (5:1), filtration, and acetone evaporation prior to fiber extraction. The pesticides were isolated with a fused-silica fiber coated with 50-microm Carbowax/template resin. The effects of pH, ion strength, sample volume, and extraction time were in…

Detection limitChromatographyChemistryPesticide ResiduesReference StandardsSolid-phase microextractionMass spectrometryTandem mass spectrometryMass SpectrometryFungicides IndustrialAnalytical ChemistryLiquid chromatography–mass spectrometryFruitDesorptionCalibrationIndicators and ReagentsSpectrophotometry UltravioletSample preparationIon trapChromatography LiquidAnalytical Chemistry
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