Search results for "acetonitrile"

showing 10 items of 1007 documents

1-Hexyl-3-methyl imidazolium tetrafluoroborate: an efficient column enhancer for the separation of basic drugs by reversed-phase liquid chromatograph…

2012

Abstract Ionic liquids are dual modifiers composed by a large anion and a large cation, which interact with both the hydrophobic alkyl-bonded phase and the anionic residual silanols in C18 columns. The deactivation of the silanol groups has important implications on the chromatographic analysis of basic drugs, being the improvement of peak profiles and shorter retention times the most noticeable features. However, other characteristics as selectivity or resolution are not usually considered, or are only examined for selected chromatographic conditions. In this work, the effect of the addition of the ionic liquid 1-hexyl-3-methyl imidazolium tetrafluoroborate to acetonitrile–water mixtures i…

Chromatography Reverse-PhaseChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryImidazolesGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryAnalytical ChemistryIonchemistry.chemical_compoundSilanolPharmaceutical PreparationsPhase (matter)Ionic liquidBoratesSelectivityAcetonitrileJournal of chromatography. A
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Application of point-to-point matching algorithms for background correction in on-line liquid chromatography–Fourier transform infrared spectrometry …

2009

A new background correction method for the on-line coupling of gradient liquid chromatography and Fourier transform infrared spectrometry has been developed. It is based on the use of a point-to-point matching algorithm that compares the absorption spectra of the sample data set with those of a previously recorded reference data set in order to select an appropriate reference spectrum. The spectral range used for the point-to-point comparison is selected with minimal user-interaction, thus facilitating considerably the application of the whole method. The background correction method has been successfully tested on a chromatographic separation of four nitrophenols running acetonitrile (0.08…

ChromatographyAbsorption spectroscopyChemistryReference data (financial markets)Analytical chemistryInfrared spectroscopyFourier transform spectroscopyAnalytical ChemistryNitrophenolschemistry.chemical_compoundSpectroscopy Fourier Transform InfraredBackground Correction MethodFourier transform infrared spectroscopySpectroscopyAcetonitrileAlgorithmsChromatography LiquidTalanta
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Retention mechanisms for basic drugs in the submicellar and micellar reversed-phase liquid chromatographic modes.

2008

The reversed-phase liquid chromatographic (RPLC) behavior (retention, elution strength, selectivity, efficiency, and peak asymmetry) for a group of basic drugs (beta-blockers), with mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) and acetonitrile, revealed different separation environments, depending on the concentrations of both modifiers: hydro-organic, submicellar at low surfactant concentration and high concentration of organic solvent, micellar, and submicellar at high concentration of both surfactant and organic solvent. In the surfactant-mediated modes, the anionic surfactant layer adsorbed on the stationary phase interacts strongly with the positively ch…

ChromatographyAcetonitrilesElutionSodium Dodecyl SulfateReversed-phase chromatographyMicelleAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantchemistryPharmaceutical PreparationsPhase (matter)SolventsSolubilitySodium dodecyl sulfateAcetonitrileMicellesChromatography LiquidAnalytical chemistry
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An approach to evaluate the information in chromatographic fingerprints: Application to the optimisation of the extraction and conservation condition…

2015

A new approach is reported for high-performance liquid chromatography to measure the level of information in fingerprints. For this purpose, the concept of peak prominence, which is the protruding part of each visible peak with regard to the valleys that delimit it, was used. The peaks in the fingerprints are ranked according to the areas of the peak prominences, and a threshold is established to discriminate between the significant peaks and those that are irreproducible. The approach was applied to evaluate the impact of several extraction conditions (solvent nature and composition, time and temperature of the treatment, amount of sample, and time and temperature of conservation of the ex…

ChromatographyAcetonitrilesPlants MedicinalTeaPlant ExtractsOrganic ChemistryExtraction (chemistry)Analytical chemistryGeneral MedicineReversed-phase chromatographyGreen teaBiochemistryChemistry Techniques AnalyticalAnalytical ChemistryLinear gradientSolventchemistry.chemical_compoundchemistrySolventsMedicinal herbsMethanolAcetonitrileChromatography High Pressure LiquidJournal of chromatography. A
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HYDRO-ORGANIC AND MICELLAR-ORGANIC REVERSED-PHASE LIQUID CHROMATOGRAPHIC PROCEDURES FOR THE EVALUATION OF SULPHONAMIDES IN PHARMACEUTICALS

2001

Two reversed-phase liquid chromatographic procedures were developed for the analysis of ten pharmaceutical formulations used in medicine and veterinary, which contained one of the following sulphonamides: sulphacetamide, sulphadiazine, sulphaguanidine, sulphamethazine, sulphamethizole, sulphamethoxazole, or sulphathiazole. In both chromatographic modes, the same C18 column was utilized and the mobile phase contained a low amount of acetonitrile and citric buffer at pH 3.0. In one of the procedures, the surfactant sodium dodecyl sul phate was added to the mobile phase. The presence of micelles allowed a decrease in the amount of organic solvent from 11% to 6%, and facilitated sample dissolut…

ChromatographyAqueous solutionElutionChemistryBiochemistry (medical)Clinical BiochemistryReversed-phase chromatographyBiochemistryMicelleDosage formAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantElectrochemistryAcetonitrileDissolutionSpectroscopyAnalytical Letters
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Analysis of pyridoquinoline derivatives by liquid chromatography/atmospheric pressure chemical ionization mass spectrometry

2001

A method using liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (LC/APCI-MS) has been developed for the characterization and determination of pyridoquinoline derivatives 4,6-bis(dimethylaminoethylamino)-2,8,10-trimethylpyrido[3,2-g]quinoline, 4,6-bis(dimethylaminoethoxy)-2,8,10-trimethylpyrido[3,2-g]quinoline and 4,6-bis[(dimethylaminoethyl)thio]-2,8,10-trimethylpyrido[3,2-g] quinoline, all with potential antitumor properties. LC separation was performed on a conventional C18 column using a binary mobile phase composed of acetonitrile and 50 mM aqueous ammonium formate at pH 3. The APCI mass spectra obtained showed that proton addition giving [M + H]+ was the…

ChromatographyAqueous solutionOrganic ChemistryQuinolineAnalytical chemistryAtmospheric-pressure chemical ionizationMass spectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryIonizationAmmonium formateMass spectrumAcetonitrileSpectroscopyRapid Communications in Mass Spectrometry
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Micellar versus hydro-organic reversed-phase liquid chromatography: a solvation parameter-based perspective.

2007

The performance of the solvation parameter model is examined for micellar liquid chromatography. The results are compared with those offered with hydro-organic eluents, intending to reveal the properties that influence the retention and distinguish the particular behaviour of micellar systems. The retention data of several series of non-ionisable and ionisable compounds (mainly steroids, polyaromatic hydrocarbons, phenols, sulfonamides, beta-blockers, phenethylamines, antihistamines, and diuretics) were used as probe compounds. The micellar mobile phases contained an anionic (sodium dodecyl sulphate), non-ionic (Brij-35), or cationic (cetyltrimethylamonium bromide) surfactant, with or witho…

ChromatographyChemistryOrganic ChemistrySolvationIonic bondingGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundSurface-Active AgentsMicellar liquid chromatographyBromideSolventsAcetonitrileMicellesChromatography LiquidJournal of chromatography. A
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Determination of Lobenzarit Disodium in Human Plasma by High-Performance Liquid Chromatography

1998

Abstract A reversed-phase high performance liquid chromatographic procedure was developed for determination of lobenzarit disodium in human plasma over the range 0.5−17.5 μg/mL with diphenylamine as internal standard. Plasma samples were extracted with acetonitrile and an aliquot was injected onto a Lichrospher 100 RP-18 column with ultraviolet absorbance detection at 308 nm. Composition of the mobile phase was acetonitrile-water-glacial acetic acid (50:50:0.2 v/v/v).

ChromatographyClinical BiochemistryDiphenylaminePharmaceutical ScienceReversed-phase chromatographyLobenzaritBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryAcetic acidchemistry.chemical_compoundchemistrymedicineCarboxylateAcetonitrileQuantitative analysis (chemistry)medicine.drugJournal of Liquid Chromatography & Related Technologies
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Determination of Phenols from Automobile Exhaust by Means of High-Performance Liquid Chromatography (HPLC)

1981

Abstract The paper describes a procedure to determine ten representative phenols (phenol, m-, p-, o-cresol, 2,4-, 2,6-, 3,4-, 3,5-xylenol, 2,3,6-, 2,4,6-trimethylphenol) in engine exhaust. Sampling was performed by a conventional Grimmer device. A sample of the water condensate collected was extracted with ether. After concentration of the ether extract phenols were isolated from other interfering compounds by stepwise elution on a Lobar column packed with LiChroprep Si 60 under controlled conditions. Relative recovery of the majority of reference phenols ranged from 90-100%. Separation of phenols into individual components was performed on polar packings as well as on Reverse Phase packing…

ChromatographyHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthAnalytical chemistrySoil ScienceEtherPollutionHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)Environmental ChemistryStepwise elutionPhenolPhenolsAcetonitrileWaste Management and DisposalQuantitative analysis (chemistry)Water Science and TechnologyInternational Journal of Environmental Analytical Chemistry
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Net analyte signal as a deconvolution-oriented resolution criterion in the optimisation of chromatographic techniques

2003

The performance of two multivariate calibration measurements, multivariate selectivity (SEL(s)) and scalar net analyte signal (scalar NAS), as chromatographic objective functions (COFs), was investigated. Since both assessments are straightforwardly related to the quantification of analytes in the presence of interferents, they were expected to confer new features in the optimisation of compound resolution, not present in conventional assessments. These capabilities are especially interesting in situations of low resolution, where peak deconvolution becomes an attractive alternative. For comparison purposes, chromatographic resolution (R(s)) and peak purity (p(s)) were used as reference COF…

ChromatographyMultivariate statisticsAnalyteAcetonitrilesChromatographyResolution (mass spectrometry)ChemistryMethanolOrganic ChemistryAnalytical chemistryPhase (waves)Scalar (physics)WaterMultivariate calibrationGeneral MedicineModels TheoreticalHydrocarbons AromaticBiochemistrySignalAnalytical ChemistryCalibrationMultivariate AnalysisSolventsDeconvolutionChromatography High Pressure LiquidJournal of Chromatography A
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