Search results for "liquid [scintillation counter]"

showing 10 items of 1764 documents

Isocratic and gradient elution in micellar liquid chromatography with Brij-35

2015

Polyoxyethylene(23)lauryl ether (known as Brij-35) is a nonionic surfactant, which has been considered as an alternative to the extensively used in micellar liquid chromatography anionic surfactant sodium lauryl (dodecyl) sulfate, for the analysis of drugs and other types of compounds. Brij-35 is the most suitable nonionic surfactant for micellar liquid chromatography, owing to its commercial availability, low cost, low toxicity, high cloud temperature, and low background absorbance. However, it has had minor use. In this work, we gather and discuss some results obtained in our laboratory with several β-blockers, sulfonamides, and flavonoids, concerning the use of Brij-35 as mobile phase mo…

Absorbancechemistry.chemical_compoundChromatographyAqueous solutionPulmonary surfactantchemistryMicellar liquid chromatographyPhase (matter)Filtration and SeparationEtherAcetonitrileMicellar electrokinetic chromatographyAnalytical ChemistryJournal of Separation Science
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Micellar liquid chromatography for prediction of drug transport.

2000

Abstract The vast majority of well absorbed drugs are transported passively across the cell membranes. Physicochemical descriptors of drug molecules that are believed to influence transcellular transport are routinely used to predict drug absorption by means of complex mathematical models. In this paper, a new in vitro method, based on the retention data in micellar liquid chromatography (MLC), is validated for the prediction of passive drug absorption. The retention of a heterogeneous drugs set in MLC using Brij 35 as surfactant in the mobile phase is compared with the retention data reported in literature obtained in red cell membrane lipid liposomes, human red cell membranes vesicles (ve…

Absorption (pharmacology)LiposomeChromatographyChemistryVesicleOrganic ChemistryCell MembraneAdministration OralGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMembranePulmonary surfactantMicellar liquid chromatographyParacellular transportHumansPharmacokineticsSpectrophotometry UltravioletMicellesChromatography LiquidJournal of chromatography. A
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Fluorimetric determination of amphetamine in urine by flow injection with on-line liquid–liquid extraction

2001

Abstract Determination of amphetamine in urine was performed by batch and flow injection methodologies. The suitable experimental conditions for fluorimetric measurements were established. The liquid–liquid extraction was carried out at pH 13 using diethyl ether as extracting reagent. The measurement conditions were 260 nm and 277 nm for excitation and emission wavelengths, respectively. The method requires standard addition calibration and Youden blank correction. The influence of the main metabolites of amphetamine and metamphetamine were studied. The accuracy and precision of the proposed method was tested and the method is adapted to the flow injection procedure with on-line extraction.

Accuracy and precisionChromatographyInjection ProcedureExtraction (chemistry)Fluorescence spectrometryAnalytical chemistryAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid–liquid extractionReagentStandard additionDiethyl etherSpectroscopyMicrochemical Journal
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Quantitative evaluation of the phenolic profile in fruits of six avocado (Persea americana) cultivars by ultra-high-performance liquid chromatography…

2016

The phenolic profiles of six varieties of avocado (Persea americana) grown in Sicily were investigated. The ultra-high-performance liquid chromatography-heated electrospray-mass spectrometry method was developed to determine qualitative and quantitative changes in fruits at two different ripening stage. Nineteen individual phenolic compounds were detected in avocado pulp extracts. Gallic acid, sinapinic acid, vanillin, p-coumaric acid, and gentisic acid were present only in ripe fruits. On the contrary, epicatechin decreased with fruit ripening, whereas protocatechuic acid, 4-hydroxybenzoic acid, chlorogenic acid, and benzoic acid were relatively stable or exhibited erratic changes with fru…

Accurate mass; Fruit ripening; High-resolution mass spectrometry; LDA; Persea americana; Phenolic compounds; Ultra-high-performance liquid chromatography; Food SciencePerseaHigh-resolution mass spectrometrySettore CHIM/10 - Chimica Degli AlimentiLDAPhenolic compoundSinapinic acid01 natural sciencesProtocatechuic acidchemistry.chemical_compound0404 agricultural biotechnologyChlorogenic acidBotanySettore CHIM/01 - Chimica AnaliticaGallic acidFood scienceGentisic acidAccurate mabiologyVanillin010401 analytical chemistryfood and beveragesRipening04 agricultural and veterinary sciencesbiology.organism_classificationFruit ripening040401 food scienceSettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreechemistryPersea americanaUltra-high-performance liquid chromatographyPhenolic compounds; Persea americana; Accurate mass; Ultra-high-performance liquid chromatography; High-resolution mass spectrometry; LDA; Fruit ripeningFood Science
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Isocratic high-performance liquid chromatographic determination of tryptophan in infant formulas.

1996

The application to infant formulas of a method for tryptophan determination by isocratic HPLC with UV detection at 254 nm, after derivatization with phenyl isothiocyanate, was studied. Protein was hydrolysed by barium hydroxide at 120 degrees C for 8 h, followed by derivatization with phenyl isothiocyanate, HPLC and UV detection at 254 nm. The optimum chromatographic conditions (pH, ionic strength of elution solvent and eluent ratio) were established. The analytical parameters (linearity, precision, accuracy of derivatization and limits of detection and quantification) were determined. The values obtained demonstrated that the method is useful for determining the tryptophan content of infan…

AcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryBarium hydroxidechemistry.chemical_compoundColumn chromatographyIsothiocyanatesHumansDerivatizationChromatography High Pressure LiquidAcetic AcidDetection limitChromatographyPhenyl isothiocyanateElutionOrganic ChemistryOsmolar ConcentrationTryptophanInfant NewbornTryptophanInfantGeneral MedicineHydrogen-Ion ConcentrationchemistrySolventsInfant FoodThiocyanatesJournal of chromatography. A
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Liquid−Liquid Equilibria for the System 1-Methyl Propyl Ethanoate (1) + Acetic Acid (2) + Water (3) at (283.15 and 323.15) K

2009

Liquid−liquid equilibrium (LLE) data for the system 1-methyl propyl ethanoate + acetic acid + water were measured at temperatures of (283.15 and 323.15) K. The temperature influence on the LLE data is very small in the temperature range studied. The NRTL and UNIQUAC models were used to correlate the data for both ternary systems. The interaction parameters obtained from both models successfully correlated the equilibrium compositions.

Acetic acidchemistry.chemical_compoundUNIQUACChromatographychemistryGeneral Chemical EngineeringNon-random two-liquid modelAnalytical chemistryLiquid liquidGeneral ChemistryAtmospheric temperature rangeTernary operationJournal of Chemical & Engineering Data
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Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
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Comparative study of solvation parameter models accounting the effects of mobile phase composition in reversed-phase liquid chromatography

2007

Solvation parameter models relate linearly compound properties with five fundamental solute descriptors (excess molar refraction, dipolarity/polarizability, effective hydrogen-bond acidity and basicity, and McGowan volume). These models are widely used, due to the availability of protocols to obtain the descriptors, good performance, and general applicability. Several approaches to predict retention in reversed-phase liquid chromatography (RPLC) as a function of these descriptors and mobile phase composition are compared, assaying the performance with a set of 146 organic compounds of diverse nature, eluted with acetonitrile and methanol. The approaches are classified in two groups: those t…

AcetonitrilesChromatographyChemistryElutionMethanolOrganic ChemistryAnalytical chemistrySolvationGeneral MedicineReversed-phase chromatographyModels TheoreticalBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySolventchemistry.chemical_compoundPolarizabilityPhase (matter)SolventsAcetonitrileChromatography LiquidJournal of Chromatography A
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Use of the modified quick easy cheap effective rugged and safe sample preparation approach for the simultaneous analysis of type A- and B-trichothece…

2010

A suitable extraction and purification method for the simultaneous liquid chromatography-mass spectrometry (LC-MS) determination of five mycotoxins, three type A, diacetoxyscirpenol (DAS), T-2 toxin (T-2) and HT-2 toxin (HT-2), and two type B-trichothecenes, deoxynivalenol (DON) and nivalenol (NIV), has been optimised using a modified "Quick Easy Cheap Effective Rugged and Safe" (QuEChERS) method. Different solvents were studied in the extraction procedure to obtain better recoveries, which ranged from 86 to 108%, using a 85/15 (v/v) mixture of methanol/acetonitrile. The values obtained for recovery, repeatability and reproducibility of the optimized method are in agreement with Commission …

AcetonitrilesChromatographyChemistryMethanolFlourOrganic ChemistryExtraction (chemistry)Wheat flourAnalytic Sample Preparation MethodsGeneral MedicineRepeatabilityQuechersBiochemistryMass SpectrometryDiacetoxyscirpenolAnalytical Chemistrychemistry.chemical_compoundVomitoxinLiquid chromatography–mass spectrometrySolventsSample preparationTrichothecenesTriticumChromatography LiquidJournal of Chromatography A
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Multi-mycotoxin analysis in wheat semolina using an acetonitrile-based extraction procedure and gas chromatography–tandem mass spectrometry

2012

A new analytical method for the rapid and simultaneous determination of ten mycotoxins including patulin, zearalenone and eight trichothecenes (nivalenol, fusarenon-X, diacetoxyscirpenol, 3-acetyl-deoxynivalenol, neosolaniol, deoxynivalenol, T-2 and HT-2) in wheat semolina has been developed and optimized. Sample extraction and purification were performed with a modified QuEChERS-based (acronym of Quick, Easy, Cheap, Effective, Rugged and Safe) procedure and determined by gas chromatography (GC) coupled to triple quadrupole instrument (QqQ). This is the first paper on the application of GC-QqQ-MS/MS to analysis of mycotoxins. Careful optimization of the gas chromatography-tandem mass spectr…

AcetonitrilesChromatographyGas Chromatography/Tandem Mass SpectrometryCalibration curveFlourLiquid-Liquid ExtractionOrganic ChemistryAnalytical chemistryReproducibility of ResultsGeneral MedicineHydrogen-Ion ConcentrationMycotoxinsQuechersSensitivity and SpecificityBiochemistryGas Chromatography-Mass SpectrometryDiacetoxyscirpenolAnalytical ChemistryTriple quadrupole mass spectrometerPatulinchemistry.chemical_compoundchemistryTandem Mass SpectrometryGas chromatographyGas chromatography–mass spectrometryJournal of Chromatography A
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