Search results for "liquid chromatography"

showing 10 items of 942 documents

Analysis of perfluorinated compounds in sewage sludge by pressurized solvent extraction followed by liquid chromatography–mass spectrometry

2011

Perfluorinated compounds (PFCs) are widely used in everyday life and one of the main recipients of these compounds is waste water treatment plants (WWTPs). Due to the structure and physicochemical properties of PFCs, these compounds could be redistributed from influent water to sludge. This work reports a new validated protocol for the analysis of 13 perfluorinated acids, 4 perfluorosulfonates and the perfluorooctanesulfonamide. The present work has been focused to develop a sensitive and robust method for the analysis of 18 PFCs in sewage sludge, based on pressurized solvent extraction (PSE) followed by solid phase extraction (SPE) clean-up, analytes separation by liquid chromatography and…

PerfluorooctanesulfonamideSensitivity and SpecificityBiochemistryAnalytical Chemistrychemistry.chemical_compoundTandem Mass SpectrometryLiquid chromatography–mass spectrometrySolid phase extractionLeast-Squares AnalysisDetection limitFluorocarbonsChromatographySewageMethanolOrganic ChemistryReproducibility of ResultsWaterGeneral MedicineRepeatabilitychemistryEnvironmental chemistryEnvironmental PollutantsSewage treatmentIon trapSludgeChromatography LiquidJournal of Chromatography A
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Evaluation and comparison of the pore structure and related properties of particulate and monolithic silicas for liquid phase separation processes

2002

Two types of silicas, highly porous beads of 10 μm average particle diameter and particle porosity between 48 to 86 % and monolithic silicas with constant mesopore diameter of 12 nm, constant total porosity of 80 % at variable macropore diameter between 2 and 6 μm were subjected to pore structural characterisation and tests in high performance liquid chromatography (HPLC). The column permeability KF of the columns packed with highly porous beads was twice as much as for the monolithic silica columns. The differences in theoretical plate height - linear velocity curves could be explained on the basis of the pore connectivity values nT of the materials which were computed from the nitrogen so…

Permeability (earth sciences)Materials sciencechemistryMacroporeChemical engineeringAnalytical chemistrychemistry.chemical_elementSorptionTheoretical plateMesoporous materialPorosityNitrogenHigh-performance liquid chromatography
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Mycotoxin Incidence in Some Fish Products: QuEChERS Methodology and Liquid Chromatography Linear Ion Trap Tandem Mass Spectrometry Approach

2019

The inclusion of vegetal raw materials in feed for fish farming has increased the risk of mycotoxin occurrence in feed, as well as in edible tissues from fish fed with contaminated feed, due to the carry-over to muscle portions. Therefore, the objective of this study was to evaluate the occurrence of 15 mycotoxins in processed fish products, which are commonly consumed, such as smoked salmon and trout, different types of sushi, and gula substitutes. A QuEChERS method was employed to perform the mycotoxin extraction from fish samples. For mycotoxin identification and quantitation, the selected technique was the liquid chromatography-tandem mass spectrometry linear ion trap (LC-MS/MS-LIT). Sm…

Pharmaceutical ScienceTandem mass spectrometry01 natural sciencesAnalytical Chemistrysushichemistry.chemical_compoundTandem Mass SpectrometryDepsipeptidesDrug Discoverymass spectrometrybiologySolid Phase ExtractionFishesfood and beverages04 agricultural and veterinary sciencesFish products040401 food scienceSmoked salmonTroutChemistry (miscellaneous)Molecular Medicineendocrine systemanimal structuresFish farmingFood ContaminationQuechersSensitivity and SpecificityArticlelcsh:QD241-4410404 agricultural biotechnologyfoodlcsh:Organic chemistrymycotoxinsFish ProductsAnimalsHumansliquid chromatographyPhysical and Theoretical ChemistryMycotoxinMuscle SkeletalfishChromatography010401 analytical chemistryOrganic Chemistrybiology.organism_classificationsmoked salmonfood.food0104 chemical sciencesSmoked fishchemistryTrichothecenesChromatography LiquidMolecules
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Estimation of the effect of the acidosis and alkalosis on the anesthetic potency of local anesthetics by biopartitioning micellar chromatography and …

2004

Local anesthetics are hydrophobic compounds and weak bases with protonation constants ranged between 7.5 and 8.8. These drugs block reversibly nerve conduction near their site of application or injection and thus produce temporary loss of feeling or sensation in a limited area of the body. The efficacy of anesthetic blockade of local anesthetics depends on the charged/uncharged form ratio and the hydrophobicity of the compounds. In addition their toxicological effects have been reported to be highly dependent on the physiological pH. Biopartitioning micellar chromatography (BMC) and micellar electrokinetic chromatography (MEKC), that use micellar solutions as mobile phases, have proven to b…

PharmacologyAlkalosisChromatographyChemistryOrganic ChemistryQuantitative Structure-Activity RelationshipAlkalosisGeneral MedicineHydrogen-Ion Concentrationmedicine.diseaseMicellar electrokinetic chromatographyPartition coefficientPulmonary surfactantMicellar liquid chromatographyDrug DiscoveryAnestheticLipophilicityMicellar solutionsmedicineAnesthetics LocalAcidosisHydrophobic and Hydrophilic Interactionsmedicine.drugChromatography LiquidChromatography Micellar Electrokinetic CapillaryEuropean journal of medicinal chemistry
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Determination of trimethylamine-N-oxide in combination withl-carnitine andγ-butyrobetaine in human plasma by UPLC/MS/MS

2015

An ultra-high-performance liquid chromatography-mass spectrometry (UPLC/MS/MS) method was developed and validated for the quantification of trimethylamine-N-oxide (TMAO) simultaneously with TMAO-related molecules L-carnitine and γ-butyrobetaine (GBB) in human blood plasma. The separation of analytes was achieved using a Hydrophilic interaction liquid chromatography (HILIC)-type column with ammonium acetate-acetonitrile as the mobile phase. TMAO determination was validated according to valid US Food and Drug Administration guidelines. The developed method was successfully applied to plasma samples from healthy volunteers.

PharmacologyAnalyteChromatographyHydrophilic interaction chromatographyClinical BiochemistryTrimethylamine N-oxideGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryHuman plasmaDrug DiscoverymedicineAmmoniumCarnitineMolecular Biologymedicine.drugBiomedical Chromatography
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Investigation into Stereoselective Pharmacological Activity of Phenotropil

2011

Phenotropil (N-carbamoylmethyl-4-aryl-2-pyrrolidone (2-(2-oxo-4-phenyl-pyrrolidin-1-yl) acetamide; carphedon)) is clinically used in its racemic form as a nootropic drug that improves physical condition and cognition. The aim of this study was to compare the stereoselective pharmacological activity of R- and S-enantiomers of phenotropil in different behavioural tests. Racemic phenotropil and its enantiomers were tested for locomotor, antidepressant and memory-improving activity and influence on the central nervous system (CNS) using general pharmacological tests in mice. After a single administration, the amount of compound in brain tissue extracts was determined using an ultra performance …

PharmacologyBiological activityGeneral MedicinePharmacologyToxicologyHigh-performance liquid chromatographyNootropicchemistry.chemical_compoundchemistryAntidepressantStereoselectivityEnantiomerAcetamideBehavioural despair testBasic & Clinical Pharmacology & Toxicology
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Dissymmetric calix[4]arenes: Optical resolution of some conformationally fixed derivatives

1993

Various possibilities to obtain intrinsically chiral calix[4]arenes are discussed. The enantiomers of three 1,3-dietheresters and one monoether compound derived from dissymmetric calix[4]arenes with C4 symmetry were separated by HPLC using chiral stationary phases and characterized by their CD spectra. © 1993 Wiley-Liss, Inc.

PharmacologyChemistryOrganic ChemistryResolution (electron density)Analytical chemistryHigh-performance liquid chromatographyCatalysisSpectral lineSymmetry (physics)Analytical ChemistryCrystallographyDrug DiscoveryEnantiomerSpectroscopyChirality
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Retention-activity relationship studies of benzodiazepines by micellar liquid chromatography

1999

Solute partitioning into lipid bilayers of biological membranes is the basis for drug and metabolite uptake, passive transport across membranes and bioaccumulation. In order to emulate in vitro the partitioning process in the biomembranes, different approaches have been proposed. The use of micellar solutions as mobile phases in reversed-phase liquid chromatography (micellar liquid chromatography, MLC) has proven to be valid in the prediction of the biological activities of local anesthetics, catecholamines and barbiturates. In this paper we focus our attention on benzodiazepines. The retention of benzodiazepines using different concentrations of Brij35 as micellar mobile phase in modified …

PharmacologyChromatographyPassive transportChemistryMetaboliteClinical BiochemistryBiological membraneGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundMembraneMicellar liquid chromatographyPhase (matter)Drug DiscoveryMicellar solutionsLipid bilayerMolecular BiologyBiomedical Chromatography
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Automated determination of clozapine and major metabolites in serum and urine.

1997

Clozapine is an atypical neuroleptic that is increasingly used for the treatment of schizophrenia. An automated method was developed for the routine quantification of clozapine and its major metabolites, N-desmethylclozapine and clozapine N-oxide, in human serum and urine by column switching and online high-performance liquid chromatography with ultraviolet detection. The method included adsorption of clozapine and its metabolites on a cyanopropyl-coated clean-up column (10 microns; 10 mm x 4.0 mm ID), washing interfering serum constituents to waste by deionized water, and, after column switching, separation on C18 ODS Hypersil reversed-phase material (5 microns; 250 mm x 4.6 mm ID). The co…

PharmacologyChromatographymedicine.diagnostic_testChemistryElutionUrineHigh-performance liquid chromatographySensitivity and SpecificityAcetic acidchemistry.chemical_compoundTherapeutic drug monitoringmedicineSchizophreniaHumansPharmacology (medical)Quantitative analysis (chemistry)ClozapineClozapineChromatography High Pressure Liquidmedicine.drugAutomated methodAntipsychotic AgentsTherapeutic drug monitoring
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Determination of phenobarbital in plasma by micellar liquid chromatography

2000

A new liquid chromatographic procedure for the determination of phenobarbital in plasma samples is described. The proposed system uses a Spherisorb octadecyl-silane ODS-2 C(18) analytical column, a guard column of similar characteristics, and a 0.03 M CTAB-3% 1-propanol at pH 7 mobile phase. The UV detector was set at 250 nm. Butabarbital was used as internal standard. Sample preparation only required the addition to the plasma samples of a 0.1 M SDS solution at pH 3 and centrifugation before injection into the chromatographic system. The limit of detection was 0.83 microg/mL of phenobarbital in plasma samples. The coefficients of variation were lower than 7. 5%.

PharmacologyDetection limitChromatographyButabarbitalChemistryClinical BiochemistryAnalytical chemistryGeneral MedicinePlasmaBiochemistryAnalytical ChemistryMicellar liquid chromatographyPhase (matter)Drug DiscoverymedicineSample preparationCentrifugationPhenobarbitalMolecular Biologymedicine.drugBiomedical Chromatography
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