Search results for "Spectroscopy"

showing 10 items of 10293 documents

FIA-Chemiluminescence Determination of Acridine Yellow

2003

Abstract The direct determination of yellow acridine is performed by a FIA assembly on the basis of the oxidation of the acridine. The acridine solution is injected into a pure water stream. This solution merges with the oxidant solution (KMnO4 in sulfuric acid medium) and the resulting chemiluminescence allows the method to be applied over the range 0.01–100 mg L−1 of acridine with a correlation coefficient of 0.9997. The relative standard deviation (%) is 1.6 and the sample throughput 60 h−1. The influence of foreign substances is also tested. The new method is applied to the determination of yellow acridine in waste waters.

ChromatographyStereochemistryBiochemistry (medical)Clinical BiochemistryRelative standard deviationSulfuric acidWater streamBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistryAcridine yellowlawAcridineElectrochemistryQuantitative analysis (chemistry)SpectroscopyChemiluminescenceAnalytical Letters
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Simultaneous dissolution profiles of two drugs in pharmaceutical formulations by an FIA manifold

2002

Abstract This article deals with the simultaneous determination of dissolution profiles of two drugs with overlapped spectra, present in the same pharmaceutical formulation. The official procedure for the dissolution profile is adapted to the continuous-flow methodology; the dissolution vessel is connected to an FIA manifold, in which the sample aliquots from the dissolution vessel are treated in order to adjust to the suitable pH and dilution degree to be monitored. The resulting solution is injected into the carrier stream, an acetic acid–acetate buffer at pH 4.3 and forced to the flow-cell of the spectrophotometer. The simultaneous determination of both profiles is based on the first der…

ChromatographySulfamethoxazoleChemistryClinical BiochemistryPharmaceutical SciencePharmaceutical formulationTrimethoprimDosage formAnalytical Chemistrylaw.inventionDilutionAnti-Infective AgentsSolubilitylawFlow Injection AnalysisDrug DiscoveryManifold (fluid mechanics)Quantitative analysis (chemistry)DissolutionSpectroscopyAnalysis methodJournal of Pharmaceutical and Biomedical Analysis
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Taxane analysis by high performance liquid chromatography-Nuclear magnetic resonance spectroscopy ofTaxus species

1998

High performance liquid chromatography–nuclear magnetic resonance spectroscopic analyses of taxane diterpenoids from three Taxus species were carried out employing a stopped-flow technique. Several taxanes have been identified from 500 mg leaf samples without prior isolation. © 1998 John Wiley & Sons, Ltd.

ChromatographyTaxanebiologyChemistryTaxus speciesTaxus × mediaPlant ScienceGeneral MedicineNuclear magnetic resonance spectroscopybiology.organism_classificationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryComplementary and alternative medicineDrug DiscoveryMagnetic resonance spectroscopicTaxus canadensisMolecular MedicineTaxaceaeFood SciencePhytochemical Analysis
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Radioactively labelled epoxides. Part III. Tritium labelled steroid 16α, 17α-epoxides

1980

Tritium labelled (17-3H) 16α, 17α-epoxy-androst-4-en-3-one and 16α, 17α-epoxy-estra-1,3,5(10)-trien-3-ol have been prepared on a large scale (200-300 mg amounts) with efficient (i.e. activity of product exactly predictable) introduction of label. The preparative method is very inexpensive, since the tritium derives from tritiated water, the steroid starting materials are readily available, and high yields are obtained in all steps.

ChromatographyTritiated waterChemistrymedicine.medical_treatmentOrganic ChemistryRadiochemistryBiochemistryAnalytical ChemistrySteroidPart iiichemistry.chemical_compoundDrug DiscoverymedicineRadiology Nuclear Medicine and imagingTritiumSpectroscopyJournal of Labelled Compounds and Radiopharmaceuticals
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Peptides analysis in blood plasma using on-line system of supported liquid membrane and high-performance liquid chromatography

2005

The potential of using supported liquid membrane (SLM) technique, combined with reversed-phase high-performance liquid chromatography (RP-HPLC) has been investigated for the determination of peptides in human blood plasma. The peptides studied were (DL)Leu(DL)Phe, MetLeuPhe, GlyLeuTyr and ValGluProlleProTyr. The carrier (Aliquat 336) was incorporated in membrane phase in order to facilitate the transport of investigated peptides. After extraction, the analyte-enriched acceptor phase was directly injected into an HPLC system for analysis. With SLM, high selectivity and efficiency were achieved for extraction of peptides in aqueous solutions. Lower extraction efficiency was obtained in plasma…

Chromatographyaliquat 336Extraction (chemistry)Analytical chemistryUltrafiltrationReversed-phase chromatographyAliquat 336BiochemistryHigh-performance liquid chromatographyAnalytical ChemistryStandard curvechemistry.chemical_compoundMembranechemistrypeptidesEnvironmental ChemistrySample preparationsupported liquid membraneHPLCSpectroscopyblood plasmaAnalytica Chimica Acta
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Supported liquid membrane extraction of aromatic aminophosphonates

2001

Abstract A fast and efficient supported liquid membrane (SLM) extraction system for the series of substituted aromatic aminophosphonates was elaborated. The mass transfer of solute was examined in terms of operator (pH and ionic strength of water phase, composition of membrane phase and the concentration of analyte) dependent parameters. Additionally, the influence of the aminophosphonates structure on the extraction efficiency was examined. From the results it can be concluded that the most effective conditions of membrane process are 10% (w/w) carrier concentration (Aliquat 336) in the liquid membrane, high pH of donor phase (pH=11) and moderate salt concentration (0.4 M NaCl) in the acce…

ChromatographyaminophosphonatesChemistryExtraction (chemistry)Inorganic chemistryAliquat 336BiochemistryAcceptorAnalytical ChemistryMembrane technologychemistry.chemical_compoundMembraneIonic strengthPhase (matter)Mass transferextractionEnvironmental Chemistrysupported liquid membraneSpectroscopyAnalytica Chimica Acta
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Quantitative retention- and migration-toxicity relationships of phenoxy acid herbicides in micellar liquid chromatography and micellar electrokinetic…

2001

Abstract The need to obtain a tool for estimation of toxicity parameters for chemicals supports, the postulation of predictive models as an alternative to conventional classical assays. The use of micellar solutions of Brij35 as mobile phases in reversed phase liquid chromatography has proven to be valid in predicting some biological activities of different kinds of drugs. In this paper, the correlations between retention of phenoxy acids using different concentrations of Brij35 as micellar mobile phase in micellar liquid chromatography (MLC) and migration in micellar electrokinetic chromatography (MEKC) with several toxicity parameters are studied. Adequate correlations retention- and migr…

ChromatographybiologyChemistrymacromolecular substancesReversed-phase chromatographybiology.organism_classificationBiochemistryDaphniaMicellar electrokinetic chromatographyAnalytical ChemistryAquatic toxicologyMicellar liquid chromatographyMicellar solutionsEnvironmental ChemistryOrganic chemistryQuantitative analysis (chemistry)Chronic toxicitySpectroscopyAnalytica Chimica Acta
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Lignans from Torreya jackii identified by stopped-flow high-performance liquid chromatography–nuclear magnetic resonance spectroscopy

1999

Abstract Coupled reversed-phase HPLC–NMR spectroscopy has been applied to the rapid detection and identification of plant metabolites of Torreya jackii , a species of Taxaceae. Analysis consisted of gradient HPLC elution and directly coupled 1 H NMR (500 MHz) spectroscopic detection in a stopped-flow mode. Seven lignans were detected and their structures were elucidated, based on their HPLC– 1 H NMR spectra and MS data. The structures were confirmed by isolation of the single components followed by conventional NMR measurements.

ChromatographybiologyElutionChemistryOrganic ChemistryAnalytical chemistryGeneral MedicineNuclear magnetic resonance spectroscopybiology.organism_classificationMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryTorreya jackiiProton NMRTaxaceaeSpectroscopyJournal of Chromatography A
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An atmospheric pressure chemical ionization-ion-trap mass spectrometer for the on-line analysis of volatile compounds in foods: a tool for linking ar…

2014

An atmospheric pressure chemical ionization ion-trap mass spectrometer was set up for the on-line analysis of aroma compounds. This instrument, which has been successfully employed for some years in several in vitro and in vivo flavour release studies, is described for the first time in detail. The ion source was fashioned from polyether ether ketone and operated at ambient pressure and temperature making use of a discharge corona pin facing coaxially the capillary ion entrance of the ion-trap mass spectrometer. Linear dynamic ranges (LDR), limits of detection (LOD) and other analytical characteristics have been re-evaluated. LDRs and LODs have been found fully compatible with the concentra…

ChromatographybiologyFlavourAnalytical chemistryEthyl hexanoateAtmospheric-pressure chemical ionizationbiology.organism_classificationMass spectrometryIon sourcechemistry.chemical_compoundchemistryIon trapSpectroscopyAromaAmbient pressureJournal of Mass Spectrometry
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Enantioseparation of phenotiazines by affinity electrokinetic chromatography using human serum albumin as chiral selector

2007

Nowadays, there is a special interest within the pharmaceutical laboratories to develop single enantiomer formulations and consequently a need for analytical methods to determine the enantiomeric purity of drugs. The present paper deals with the enantiomeric separation of promethazine and trimeprazine enantiomers by affinity electrokinetic chromatography (AEKC)-partial filling technique using human serum albumin (HSA) as chiral selector. A multivariate optimization of the most critical experimental variables in enantioresolution, running pH, HSA concentration and plug length, is carried out to obtain enantioresolution of promethazine and trimeprazine. The estimated maximum and optimum resol…

ChromatographybiologyResolution (mass spectrometry)TrimeprazineSerum albuminHuman serum albuminBiochemistryAnalytical ChemistryPromethazinechemistry.chemical_compoundAffinity chromatographychemistryPhenothiazinebiology.proteinmedicineEnvironmental ChemistryEnantiomerSpectroscopymedicine.drugAnalytica Chimica Acta
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