Search results for "Liquid Chromatography"

showing 10 items of 942 documents

High-performance liquid chromatography of amino acids, peptides and proteins

1990

Abstract The thermodynamic constants, associated with the interaction of three proteins with triazine dye affinity sorbents, have been derived from bath and frontal analysis experiments. In cases where mass-transfer restrictions are very high, calculation of the thermodynamic constants directly from frontal analysis experiments could not be achieved. In such cases, a portion of the adsorbate was always present in the effluent, a situation which has its effect as the split peak phenomenon. With Fractogel-based triazine dye affinity sorbents none of the test proteins applied in frontal analysis were adsorbed. A similar behaviour was observed for a Cellufine sorbent during the adsorption of hu…

SorbentChromatographyLigandChemistryDiffusionKineticsOrganic ChemistryGeneral MedicineHuman serum albuminBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundAdsorptionmedicineParticleLysozymePorositySaturation (chemistry)medicine.drugTriazineJournal of Chromatography A
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Pesticide analysis in coffee leaves using a quick, easy, cheap, effective, rugged and safe approach and liquid chromatography tandem mass spectrometr…

2017

An analytical method using a quick, easy, cheap, effective, rugged and safe (QuEChERS) procedure for multi-residue determination of 52 pesticides in coffee leaf extractshas been developed and validated according to SANTE/11945/2015 guidelines. Different sorbent combinations for dispersive solid phase extraction (d-SPE) clean-up as well as dispersive liquid-liquid microextraction (DLLME) were tested. The relative standard deviations (RSDs) for the recovery of 87-94% of pesticides added to coffee leaf extracts,was ≤20% for samples spiked at concentrations up to 50ng*g-1 depending on the clean-up procedures. However, samples spiked with a 100ng*g-1 pesticide mixture gave RSDs>20% for most pest…

SorbentCoffeaFood Contamination010402 general chemistryQuechers01 natural sciencesBiochemistryCoffeeAnalytical ChemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometrySolid phase extractionChromatographyChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Solid Phase ExtractionPesticide ResiduesGeneral MedicineOrganic coffeePesticide0104 chemical sciencesClean-upPlant LeavesAdsorptionChromatography LiquidJournal of chromatography. A
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Modified magnetic-based solvent-assisted dispersive solid-phase extraction: application to the determination of cortisol and cortisone in human saliv…

2021

A modification of magnetic-based solvent-assisted dispersive solid-phase extraction (M-SA-DSPE) has been employed for the determination of the biomarkers cortisol and cortisone in saliva samples. M-SA-DSPE is based on the dispersion of the sorbent material by using a disperser solvent like in dispersive solid phase extraction (SA-DSPE) but a magnetic sorbent is used like in magnetic dispersive solid-phase extraction (M-DSPE). Thus, the magnetic sorbent containing the target analytes is retrieved using an external magnet like in M-DSPE. Finally, the analytes are desorbed into a small volume of organic solvent for the subsequent chromatographic analysis. To this regard, a M-SA-DSPE-based meth…

SorbentHydrocortisone010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryHumansSolid phase extractionSalivaDetection limitChromatographyChemistryMagnetic Phenomena010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Solid Phase ExtractionGeneral MedicineRepeatability0104 chemical sciencesSolventCortisoneSolventsMagnetic nanoparticlesChromatography LiquidJournal of chromatography. A
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Sample preparation strategies for the determination of psychoactive substances in biological fluids

2020

This review focuses on the existing analytical procedures for the determination of new psychoactive substances (NPS) in biological fluids by chromatographic methods. Direct analysis of samples is scarcely employed and most proposed methodologies include a sample pre-treatment in order to remove matrix interferents and, in some cases, pre-concentrate extracts. Current extraction methods for NPS determination in plasma/serum, urine, and oral fluids have been widely discussed, such as liquid-liquid, solid-phase, and micro extraction approaches, highlighting the advantages and drawbacks of the proposed extraction methodologies. Regarding microextraction approaches, techniques like microextracti…

SorbentLiquid Phase MicroextractionLiquid-Liquid ExtractionClinical Chemistry Tests010402 general chemistry01 natural sciencesBiochemistrySpecimen HandlingAnalytical ChemistryMatrix (chemical analysis)Liquid chromatography–mass spectrometryBiological fluidsHumansSample preparationSolid phase extractionSalivaSolid Phase MicroextractionChromatographyPsychotropic DrugsChromatographyChemistrySolid Phase Extraction010401 analytical chemistryOrganic ChemistryExtraction (chemistry)General MedicineBody Fluids0104 chemical sciencesAnalytical proceduresJournal of Chromatography A
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Biomarkers to disclose recent intake of alcohol: potential of 5-hydroxytryptophol glucuronide testing using new direct UPLC-tandem MS and ELISA metho…

2007

Aims: This study compared two new methods for direct determination of 5-hydroxytryptophol glucuronide (GTOL) in urine, a biomarker for detection of recent alcohol consumption. Methods: Urine samples were collected from ten alcoholic patients during recovery from intoxication. A direct injection ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for measurement of the urinary GTOL to 5-hydroxyindoleacetic acid (5-HIAA) ratio, and an ELISA assay for direct measurement of GTOL, were used. Comparison was made with the urinary ethanol and ethyl glucuronide (EtG) concentrations. Results: The breath ethanol concentration on admission ranged between 1.0-3.1 g/l. Th…

Spectrometry Mass Electrospray IonizationAlcohol DrinkingUrinary systemEnzyme-Linked Immunosorbent AssayAlcoholUrineHigh-performance liquid chromatographychemistry.chemical_compoundGlucuronidesEthyl glucuronideTandem Mass SpectrometryHumansMedicineChromatography High Pressure LiquidEthanolChromatographyEthanolbusiness.industryCentral Nervous System DepressantsGeneral MedicineHydroxyindoleacetic AcidAlcoholismBreath TestschemistryBiochemistryHydroxytryptopholBiomarker (medicine)GlucuronidebusinessBiomarkersAlcohol and Alcoholism
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Mycotoxin Identification and In Silico Toxicity Assessment Prediction in Atlantic Salmon

2020

The present study aimed to identify mycotoxins in edible tissues of Atlantic salmon (Salmo salar) using liquid chromatography coupled to hybrid quadrupole time-of-flight mass spectrometry (LC-Q-TOF-MS). After using a non-targeted screening approach and a home-made spectral library, 233 mycotoxins were analyzed. Moreover, the occurrence of mycotoxins in fish filets was evaluated, and their potential toxicity was predicted by in silico methods. According to the obtained results, forty mycotoxins were identified in analyzed salmon samples, the predominant mycotoxins being enniatins (also rugulosin and 17 ophiobolins), commonly found in cereals and their by-products. Thus, mycotoxin carry-over …

Spectrometry Mass Electrospray IonizationAtlantic salmonin silico predictionIn silicoSalmo salarPharmaceutical ScienceFood ContaminationAquacultureRisk Assessment01 natural sciencesArticleOphiobolinschemistry.chemical_compound0404 agricultural biotechnologymycotoxinsDrug DiscoveryAnimalsliquid chromatographyComputer SimulationFood scienceSalmoMycotoxinlcsh:QH301-705.5Pharmacology Toxicology and Pharmaceutics (miscellaneous)Chromatography High Pressure Liquidbiology010401 analytical chemistry04 agricultural and veterinary sciencestime of flight mass spectrometrybiology.organism_classificationAnimal Feed040401 food scienceToxicokinetics0104 chemical sciencesSeafoodlcsh:Biology (General)chemistryMycotoxin identificationToxicityFish <Actinopterygii>Potential toxicityMarine Drugs
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Determination of dithiocarbamates and metabolites in plants by liquid chromatography–mass spectrometry

2004

Abstract A quantitative matrix solid-phase dispersion and liquid chromatography–atmospheric pressure chemical ionization mass spectrometry (LC–APCI–MS) method is outlined for the simultaneous analysis of dithiocarbamates (DTCs) and their degradation products in plants. Compounds analyzed are dazomet, disulfiram, thiram and the metabolites ethylenthiourea and propylenthiourea. The performance of two different sample preparation protocols, the proposed one and other based on solid-phase extraction, as well as, of both atmospheric pressure ionization sources, APCI and electrospray, were compared. The effect of several parameters on the extraction, separation and detection was studied. Dithioca…

Spectrometry Mass Electrospray IonizationChemical ionizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicinePlantsReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ThiocarbamatesLiquid chromatography–mass spectrometryFruitVegetablesIndicators and ReagentsSample preparationSolid phase extractionChromatography LiquidJournal of Chromatography A
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Identification and quantification of phosphatidylcholines containing very-long-chain polyunsaturated fatty acid in bovine and human retina using liqu…

2010

The retina is one of the vertebrate tissues with the highest content in polyunsaturated fatty acids (PUFA). A large proportion of retinal phospholipids, especially those found in photoreceptor membranes, are dipolyunsaturated molecular species. Among them, dipolyunsaturated phosphatidylcholine (PC) molecular species are known to contain very-long-chain polyunsaturated fatty acids (VLC-PUFA) from the n-3 and n-6 series having 24-36 carbon atoms (C24-C36) and four to six double bonds. Recent interest in the role played by VLC-PUFA arose from the findings that a protein called elongation of very-long-chain fatty acids 4 (ELOVL4) is involved in their biosynthesis and that mutations in the ELOVL…

Spectrometry Mass Electrospray IonizationChimie analytiquePhospholipidChromosome DisordersTandem mass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyRetinaAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundMacular Degeneration[CHIM.ANAL]Chemical Sciences/Analytical chemistryTandem Mass SpectrometryPhosphatidylcholineQUANTITATIVE ANALYSISAnimalsHumansOxazolesChromatography High Pressure Liquid030304 developmental biologychemistry.chemical_classificationPhosphatidylethanolamine0303 health sciencesVERY LONG CHAIN POLYUNSATURATED FATTY ACIDSChromatography010401 analytical chemistryOrganic ChemistryPHOSPHATIDYLCHOLINES;QUANTITATIVE ANALYSIS;LC-ESI-MS/MS;VERY LONG CHAIN POLYUNSATURATED FATTY ACIDS;RETINAGeneral MedicineLC-ESI-MS/MSeye diseases0104 chemical scienceschemistryBiochemistryDocosahexaenoic acidFatty Acids UnsaturatedPhosphatidylcholines[ CHIM.ANAL ] Chemical Sciences/Analytical chemistrylipids (amino acids peptides and proteins)CattleChromosomes Human Pair 6SphingomyelinPolyunsaturated fatty acidJournal of chromatography. A
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Routine application using single quadrupole liquid chromatography-mass spectrometry to pesticides analysis in citrus fruits.

2005

Abstract A rapid and sensitive liquid chromatography–electrospray ionization–mass spectrometry method has been developed for the routine analysis of buprofezin, bupirimate, hexaflumuron, tebufenpyrad, fluvalinate and pyriproxyfen in citrus fruits. Extracts were obtained by matrix solid-phase dispersion (MSPD) using C 18 as dispersant and dichloromethane-methanol (80:20, v/v) as eluent. Matrix effects were tested for all matrices by addition of standard to sample blank extracts (samples containing no detectable residues). Mean recoveries obtained at fortification levels between 0.01 and 5 mg kg −1 were 57–97% with relative standard deviations (RSDs) from 5 to 19%. The limits of quantificatio…

Spectrometry Mass Electrospray IonizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerMatrix (chemical analysis)Liquid chromatography–mass spectrometryFruitmedia_common.cataloged_instanceSample preparationSolid phase extractionEuropean unionPesticidesmedia_commonChromatography LiquidJournal of chromatography. A
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Comparison of four mass analyzers for determining carbosulfan and its metabolites in citrus by liquid chromatography/mass spectrometry

2006

Four liquid chromatography/mass spectrometry (LC/MS) systems, equipped with single quadrupole, triple quadrupole (QqQ), quadrupole ion trap (QIT) and quadrupole time-of-flight (QqTOF) mass analyzers, were evaluated for the analysis of carbosulfan and its main transformation products. The comparison of quantitative aspects (sensitivity, precision and accuracy) was emphasized. Results showed that the triple quadrupole instrument reaches at least 20-fold higher sensitivity (LOD from 0.04 to 0.4 microg kg(-1)) compared to the single quadrupole (4-70 microg kg(-1)), the QIT (4-25 microg kg(-1)) and the QqTOF (4-23 microg kg(-1)) instruments. Recoveries were over 70% for all the analytes, except …

Spectrometry Mass Electrospray IonizationChromatographyOrganic ChemistryAnalytical chemistryReproducibility of ResultsButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerDibutylamineCarbofuranchemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryQuadrupoleCarbosulfanCarbamatesQuadrupole ion trapChromatography High Pressure LiquidSpectroscopyCitrus sinensisRapid Communications in Mass Spectrometry
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