Search results for "liquid chromatography"

showing 10 items of 942 documents

Automated determination of reboxetine by high-performance liquid chromatography with column-switching and ultraviolet detection.

2000

A fully automated method including column-switching and isocratic high-performance liquid chromatography (HPLC) was developed for quantitative analysis of the new antidepressant reboxetine, a noradrenaline reuptake inhibitor. After serum injection into the HPLC system and on-line sample clean-up on a silica C8 (10x4.0 mm I.D.) clean-up column with an eluent consisting of 2.5% acetonitrile in deionized water, the chromatographic separation was performed on an analytical column (Lichrospher CN; 250x4.6 mm I.D.) with an eluent of acetonitrile-aqueous potassium phosphate buffer (0.008 M, pH 6.4) (50:50). The UV detector was set at 273 or 226 nm. The limit of quantification was about 15 ng/ml at…

Detection limitQuality ControlChromatographymedicine.diagnostic_testAdrenergic Uptake InhibitorsReboxetineMorpholinesAnalytical chemistryGeneral ChemistryHigh-performance liquid chromatographychemistry.chemical_compoundAutomationReboxetineColumn chromatographychemistryPotassium phosphateTherapeutic drug monitoringSpectrophotometrymedicineHumansSpectrophotometry UltravioletQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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Determination of abamectin in citrus fruits by liquid chromatography-electrospray ionization mass spectrometry.

2000

Liquid chromatography coupled to electrospray mass spectrometry (LC-ES-MS) with positive ion detection was used to determine abamectin in oranges. MS conditions were optimized to achieve maximum sensitivity. The main ion for abamectin was [M+Na]+ at a fragmentor voltage of 180 V. Abundant structural information can be obtained at different fragmentor voltages. The detection limit for the standard solution was 12 pg injected, and good linearity and reproducibility were observed. Abamectin residues were extracted using matrix solid-phase dispersion. Orange samples were homogenized with C18 bonded silica placed onto a glass column and eluted with dichloromethane. Recoveries of the abamectin fr…

Detection limitQuality ControlElectrosprayCitrusInsecticidesChromatographyIvermectinElutionElectrospray ionizationOrganic ChemistryReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryAbamectinSolid phase extractionChromatography High Pressure LiquidJournal of chromatography. A
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Derivatization techniques for automated chromatographic analysis of amphetamine usingo-phthaldialdehyde: A comparative study

2000

The potential of different chromatographic systems for automated, on-line analysis of amphetamine in biological fluids is illustrated. The various systems integrate analyte purification and enrichment, separation, derivatization in different derivatization modes witho-phthaldialdehyde (OPA) and N-acetyl-L-cysteine (NAC), and fluorimetric detection. The reliability of the systems has been tested by analysing urine and plasma samples containing amphetamine in the 0.1–20.0 μg mL−1 range. Pre, on and post-column derivatization strategies are compared in terms of their instrumental requirements, selectivity, sensitivity, linearity and reproducibility.

Detection limitReproducibilityAnalyteChromatographyOrganic ChemistryClinical BiochemistryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineSample preparationAmphetamineDerivatizationQuantitative analysis (chemistry)medicine.drugChromatographia
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Automated determination of amisulpride by liquid chromatography with column switching and spectrophotometric detection.

2003

A fully automated chromatographic method including on-line blood serum or plasma clean-up, isocratic high-performance liquid chromatography (HPLC) and spectrophotometric detection was developed for quantitative analysis of the new antipsychotic drug amisulpride. After injection of serum or plasma onto the HPLC system and clean-up on a pre-column (10x4.0 mm I.D.) filled with Silica CN 20 micrometer (pore size 10 nm) by an eluent consisting of 8% acetonitrile in deionized water, the chromatographic separation was performed on Lichrospher CN (5 micrometer; 250x4.6 mm I.D.) by an eluent consisting of 50% acetonitrile and 50% aqueous potassium phosphate buffer (0.008 M, pH 6.4). The UV detector …

Detection limitReproducibilityChromatographyClinical BiochemistryAnalytical chemistryCell BiologyGeneral MedicineReference StandardsBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyBlood serumchemistryPotassium phosphateSpectrophotometryHumansAmisulprideSulpirideAcetonitrileQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Multimycotoxin LC-MS/MS Analysis in Tea Beverages after Dispersive Liquid-Liquid Microextraction (DLLME).

2017

The aim of the present study was to develop a multimycotoxin liquid chromatography tandem mass spectrometry (LC-MS/MS) method with a dispersive liquid-liquid microextraction procedure (DLLME) for the analysis of AFs, 3aDON, 15aDON, NIV, HT-2, T-2, ZEA, OTA, ENNs, and BEA in tea beverages and to evaluate their mycotoxin contents. The proposed method was characterized in terms of linearity, limits of detection (LODs), limits of quantification (LOQs), recoveries, repeatability (intraday precision), reproducibility (interday precision), and matrix effects to check suitability. The results show LODs in the range of 0.05-10 μg/L, LOQs in the range of 0.2-33 μg/L, and recoveries in the range of 65…

Detection limitReproducibilityChromatographyTeaChemistryLiquid Phase Microextraction010401 analytical chemistryFood Contamination04 agricultural and veterinary sciencesGeneral ChemistryRepeatabilityMycotoxinsGreen tea040401 food science01 natural sciences0104 chemical scienceschemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryLimit of DetectionTandem Mass SpectrometryLc ms msLiquid liquidGeneral Agricultural and Biological SciencesMycotoxinJournal of agricultural and food chemistry
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Thermal Lens Spectrometric Detection of Catecholamines after Oxidation to Aminochromes

1992

Abstract Experimental conditions for the spectrophotometric and thermal lens spectrometry (TLS) detection of catecholamines after oxidation to aminochromes with hexacyanoferrate (III) are optimized. At the low concentrations used in TLS, and in a 0.07 M citrate buffer, catecholamine oxidation can be performed at pH 7 and is immediate, whereas a lower pH value is required in spectrophotometry to avoid aminochrome polymerisation, the oxidation reactions being much slower. Similar TLS sensitivities are obtained for all catecholamines which facilitates HPLC evaluation. Sensitivity can be enhanced using a 50% ethanol-water medium. The linear dynamic range extends over two orders of magnitude, th…

Detection limitReproducibilityChromatographymedicine.diagnostic_testChemistryBiochemistry (medical)Clinical BiochemistryMass spectrometryBiochemistryRedoxHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionLens (optics)lawSpectrophotometryElectrochemistrymedicineUrine sampleSpectroscopyAnalytical Letters
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Determination of benzoylurea insecticides in food by pressurized liquid extraction and LC-MS

2010

A method based on pressurized liquid extraction and LC-MS/MS has been developed for determining nine benzoylureas (BUs) in fruit, vegetable, cereals, and animal products. Samples (5 g) were homogenized with diatomaceous earth and extracted in a 22 mL cell with 22 mL of ethyl acetate at 80 degrees C and 1500 psi. After solvent concentration and exchange to methanol, BUs were analyzed by LC-MS/MS using an IT mass analyzer, which achieved several transitions of precursor ions that increase selectivity providing identification. LOQs were between 0.002 and 0.01 mg/kg, which are equal or lower than maximum residue limits established by the Codex Alimentarius. Excellent linearity was achieved over…

Detection limitResidue (complex analysis)ChromatographyBenzoylureaExtraction (chemistry)Ethyl acetateFiltration and SeparationHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometrymedicineSample preparationmedicine.drugJournal of Separation Science
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Multi-class determination of antimicrobials in meat by pressurized liquid extraction and liquid chromatography–tandem mass spectrometry

2008

A multi-residue method using pressurized liquid extraction (PLE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed for determining trace levels of 31 antimicrobials, including beta-lactams, lincosamides, macrolides, quinolones, sulfonamides, tetracyclines, nitroimidazoles and trimethoprim. The extraction method required pre-homogeneization of the meat with EDTA-washed sand and subsequent one-static-cycle extraction for 10 min with 40 ml of water at 1500 psi and 70 degrees C. The effect of operation temperature, pressure, flush volume, and static cycles on PLE performance was studied. Average recoveries ranged from 75 to 99% with relative standard deviations <1…

Detection limitResidue (complex analysis)MeatChromatographyMolecular StructureSwineChemistryOrganic ChemistryReproducibility of ResultsGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnti-Bacterial AgentsAnalytical ChemistryHot water extractionTandem Mass SpectrometryLiquid chromatography–mass spectrometryAnimalsmedia_common.cataloged_instanceCattleSample preparationEuropean unionChromatography LiquidAntibacterial agentmedia_commonJournal of Chromatography A
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Determinación de residuos de paraquat en lechuga y repollo cultivados en Lepaterique mediante HPLC-DAD

2018

La determinación de residuos del herbicida paraquat en lechuga (Lactuca sativa) y repollo (Brassica oleracea) producidos en la comunidad de La Brea, Lepaterique y comercializados en la ciudad de Tegucigalpa fue llevada a cabo en los meses de octubre y noviembre de 2017, mediante la aplicación de cromatografía líquida de elevada resolución con detector de arreglo de diodos (HPLC-DAD) en menos de 6 minutos, con un mecanismo de separación de fase reversa empleando una columna superficialmente porosa C18 y una mezcla de ácido orto fosfórico al 0.1 M (pH 3,0) con acetonitrilo en proporción de 3:1 como fase móvil. El método se basa en la extracción con baño ultrasónico utilizando agua como solven…

Detection limitSolventChromatographyMaximum Residue LimitIon exchangeChemistryElutionExtraction (chemistry)Solid phase extractionHigh-performance liquid chromatographyPortal de la Ciencia
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Selective solid-phase extraction of organophosphorus pesticides and their oxon-derivatives from water samples using molecularly imprinted polymer fol…

2020

Abstract A molecularly imprinted polymer was synthesized and characterized to be used as solid-phase extraction sorbent for simultaneous chlorpyrifos and diazinon and their oxon derivatives. Several imprinted polymers were prepared and evaluated in a retention study of these analytes compared with a non-printed polymer. Several parameters affecting the extraction of imprinted polymer such as washing solvent, composition and volume of the eluting solvent and sample volume, were also investigated. Under the optimum conditions, the developed method provided satisfactory limits of detection ranging between 0.07 µg L−1 to 0.12 µg L−1 and the material showed an excellent reusability (> 50 reuses)…

Detection limitSorbentChromatographyOxonPolymersSolid Phase ExtractionOrganic ChemistryExtraction (chemistry)Molecularly imprinted polymerFresh WaterGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMolecular ImprintingSolventchemistry.chemical_compoundchemistryLimit of DetectionDiazinonSpectrophotometry UltravioletChlorpyrifosSolid phase extractionPesticidesChromatography High Pressure LiquidJournal of Chromatography A
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