Search results for "Liquid Chromatography"

showing 10 items of 942 documents

Liquid chromatography and characterization of ether-functionalized imidazolium ionic liquids on mixed-mode reversed-phase/cation exchange stationary …

2010

Abstract A new series [CnOmmim]Cl of imidazolium cation-based ionic liquids (ILs), with an ether functional group on the alkyl side-chain, has been prepared. The possibility of analyzing the ionic liquids by high performance liquid chromatography (HPLC) was investigated on mixed-mode reversed/cation exchange stationary phase with the aqueous-acetonitrile mobile phase. Elution parameters, such as retention factor, selectivity and column efficiency, were studied as functions of mobile phase composition and pH. The ILs were characterized by elemental analysis, and infrared, UV and 1H, 13C NMR spectroscopy.

ChromatographyChemistryElutionGeneral Chemical EngineeringHydrophilic interaction chromatographyIon chromatographyAnalytical chemistryEtherGeneral ChemistryReversed-phase chromatographyHigh-performance liquid chromatographychemistry.chemical_compoundPhase (matter)Ionic liquidComptes Rendus Chimie
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Univariate method for background correction in liquid chromatography–Fourier transform infrared spectrometry

2007

An univariate method is proposed for background correction in on-line gradient liquid chromatography-Fourier transform infrared (LC-FTIR) spectrometry using acetonitrile:water as mobile phase components. The method is based on the calculation of the ratio of absorbances (AR) at two characteristic wavenumbers for each spectrum. This parameter is subsequently used to locate the most appropriated eluent spectrum within a reference spectra matrix (RSM) to be subtracted from each spectrum included in the sample chromatogram. To correct minor changes in eluent spectra intensity during the elution of analytes, a correction factor (Kf), defined as the ratio of the absorbance of the sample and the s…

ChromatographyChemistryElutionOrganic ChemistryAnalytical chemistryInfrared spectroscopyGeneral MedicineReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ChemometricsAbsorbanceDiuronSpectroscopy Fourier Transform InfraredAtrazineFourier transform infrared spectroscopyChromatography LiquidJournal of Chromatography A
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Extraction of clenbuterol from calf urine using a molecularly imprinted polymer followed by quantitation by high-performance liquid chromatography wi…

2002

A method for the extraction of clenbuterol from calf urine samples using a molecularly imprinted polymer (MIP) has been developed. The aim was that the final extracts from the MIP should allow quantitation of clenbuterol down to 0.5 ng/mL urine using HPLC with UV detection. The MIP was produced using brombuterol as a template and the selectivity of the MIP, for clenbuterol, was tested against a non-imprinted polymer (produced without template) and was found to be high. After loading of 5 mL diluted centrifuged urine, selective binding was established in acetonitrile-acetic acid (98:2). For further elution of interferences, 0.5 M ammonium acetate buffer pH 5 and 70% acetonitrile in water was…

ChromatographyChemistryElutionOrganic ChemistryExtraction (chemistry)Molecularly imprinted polymerReproducibility of ResultsGeneral MedicineReversed-phase chromatographyReference StandardsSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryClenbuterolmedicineAnimalsCattleClenbuterolSpectrophotometry UltravioletSample preparationSolid phase extractionAdrenergic alpha-AgonistsChromatography High Pressure Liquidmedicine.drugJournal of Chromatography A
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Liquid chromatographic procedure for the evaluation of β-blockers in pharmaceuticals using hybrid micellar mobile phases

1997

Abstract A reversed-phase chromatographic procedure with a micellar eluent is proposed for the determination of several β-blockers (acebutolol, atenolol, carteolol, celiprolol, labetalol, metoprolol, nadolol, oxprenolol, propranolol, and timolol) in pharmaceutical formulations (tablets, capsules, and ophthalamic solutions). A study is shown on the chromatographic behaviour of these drugs with mobile phases containing sodium dodecyl sulphate (0.075–0.15 M ) and propanol (0–15%, v/v), at different pH values (3–7). The excellent correlation between log of the octanol-water partition coefficient and log of capacity factor, for the ten drugs in mobile phases of SDS and propanol, suggested that t…

ChromatographyChemistryElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyCapacity factorDosage formAnalytical ChemistryPartition coefficientPropanolchemistry.chemical_compoundOxprenololmedicinemedicine.drugJournal of Chromatography A
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Solid-Phase Extraction Techniques for Assay of Diuretics in Human Urine Samples

1991

Abstract Solid-phase extraction techniques were evaluated for the treatment of urine samples in the analysis of diuretics before injection into an HP-Hypersyl ODS-C18 column. Six different reversed-phase extraction columns were tested, and the results obtained are compared with those obtained in a classical liquid-liquid extraction with ethyl acetate. The solid-phase extraction procedures are the best overall choice for all the diuretics tested, due to their versatility, the minor time-consuming, and the good recovery percentages obtained. C18 and C8 packings give the highest recoveries for a majority of the diuretics studied. However, CH or PH columns, due to their greater selectivity, can…

ChromatographyChemistryElutionmedicine.medical_treatmentExtraction (chemistry)Ethyl acetateHigh-performance liquid chromatographyMatrix (chemical analysis)chemistry.chemical_compoundmedicineMolecular MedicineSolid phase extractionDiureticThiazidemedicine.drugJournal of Liquid Chromatography
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Determination of tetracyclines in multi-specie animal tissues by pressurized liquid extraction and liquid chromatography–tandem mass spectrometry

2009

Abstract A specific, sensitive and robust pressurized liquid extraction (PLE) and liquid chromatography tandem mass spectrometry (LC–MS/MS) method for determining tetracycline, chlortetracycline, oxytetracycline and doxycycline in bovine, swine, poultry and lamb muscle tissues is presented. PLE was performed using an ASE ® 200 from Dionex and water as extractant, followed by solid-phase extraction (SPE) using an Oasis HLB cartridge. The method was validated for beef, chicken, pork and lamb meat in compliance with the requirements set by Commission Decision, 2002/657/EC [Commission Decision 2002/657/EC (2002). Implementing Council Directive 96/23/EC concerning the performance of analytical m…

ChromatographyChemistryExtraction (chemistry)General MedicineOxytetracyclineMass spectrometryAnalytical ChemistryLiquid chromatography–mass spectrometrymedicinemedia_common.cataloged_instanceSample preparationSolid phase extractionEuropean unionQuantitative analysis (chemistry)Food Sciencemedicine.drugmedia_commonFood Chemistry
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A new derivatization procedure for the determination of cephalexin with 1,2-naphthoquinone 4-sulphonate in pharmaceutical and urine samples using sol…

1998

Abstract The present report shows how to derivatize cephalexin with 1,2-naphthoquinone-4-sulphonate (NQS) into solid-phase extraction cartridges (C18) using UV–visible detection. Optimum conditions for this new procedure are: hydrogen carbonate/carbonate buffer pH=10.5, 5 min reaction time at 25°C and NQS concentration of 7.1×10−3 mol l−1. The accuracy and the precision of the method were tested. The procedure was used to measure cephalexin in pharmaceutical and urine samples. The results obtained were contrasted with those reported by UV-spectrophotometric and HPLC methods for pharmaceutical samples and with HPLC method for urine samples. The H-point standard additions method was used to m…

ChromatographyChemistryExtraction (chemistry)NQSBiochemistryHigh-performance liquid chromatographyDosage formAnalytical Chemistrychemistry.chemical_compoundStandard additionEnvironmental ChemistrySolid phase extractionDerivatizationSpectroscopyAntibacterial agentAnalytica Chimica Acta
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Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

1999

A rapid, sensitive and reproducible high-performance liquid chromatographic assay for busulfan in human plasma was developed. After extraction of plasma samples with acetonitrile and methylene chloride, busulfan and the internal standard [1,5-bis(methanesulfonyloxy)pentane] were derivatized with 8-mercaptoquinoline to yield fluorescent compounds which were detected with a fluorescence detector equipped with filters of 360 nm (excitation) and 425 nm (emission). Calibration graphs showed a linear correlation (r>0.9990) over the concentration range of 20-2000 ng/ml. The recovery of busulfan from plasma standards was 70+/-5%. The detection and quantification limits for busulfan in plasma sample…

ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral ChemistryReference StandardsHigh-performance liquid chromatographyFluorescenceSensitivity and SpecificityFluorescence spectroscopyPentanechemistry.chemical_compoundSpectrometry FluorescenceCalibrationmedicineHumansDerivatizationQuantitative analysis (chemistry)Antineoplastic Agents AlkylatingBusulfanBusulfanChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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New Alternative in the Methodology of Extraction and Dyeing with Active Molecules Derived from Vegetal Sources

2016

Abstract The general objective of this study refers to the identification of a sustainable and physical methodology of extraction of active compounds, envisaging the preservation of the high purity active natural dye molecule from nut shell (juglone), even under the conditions of an extraction performed in a mixt solvent medium (water-ethanol). The second major objective of the study consists of the application of these above mentioned dyes onto natural and synthetic substrates, thus making a correlation between their colour attributes and the fibrous composition of the substrates they are applied on. The motivation of this research was given by the identification of an improved extraction …

ChromatographyChemistryExtraction (chemistry)green walnut shellsjugloneInfrared spectroscopy04 agricultural and veterinary sciences040401 food scienceHigh-performance liquid chromatographySolventchemistry.chemical_compound0404 agricultural biotechnologyFT-RAMAN.FT-IR spectroscopyGeneral Earth and Planetary SciencesOrganic chemistryMoleculeUS extractioncoloristic attributeDyeingNatural dyeJugloneGeneral Environmental ScienceProcedia Technology
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Simultaneous isolation of xanthomegnin, viomellein, rubrosulphin, viopurpurin, and brevianamide A by preparative HPLC.

1984

A method for the isolation of xanthomegnin, viomellein, rubrosulphin, viopurpurin, and brevianamide A from Penicillium viridicatum (DSM 2447) is described. After extraction, HPLC was performed with a preparative silicagel column, eluted with toluene / ethyl acetate / formic acid (27/9/1, v/v/v) and dichloromethane / acetic acid (9/1, v/v). The toxins were detected with a UV-monitor. It was possible to isolate them in an absolutely pure state. The described method is operationally simple and very efficient.

ChromatographyChemistryFormic acidExtraction (chemistry)Ethyl acetateToxicologyMicrobiologyTolueneHigh-performance liquid chromatographychemistry.chemical_compoundAcetic acidPenicillium viridicatumBiotechnologyDichloromethaneMycotoxin research
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