Search results for "Tandem"

showing 10 items of 560 documents

Statistical Approach for Biomarker Discovery Using Label-Free LC-MS Data: An Overview

2016

The identification of new diagnostic, prognostic, or theranostics biomarkers is one of the main aims of clinical research. Technologies like mass spectrometry (MS) focus on the discovery of proteins as biomarkers and are commonly being used for this purpose. Mass spectrometry consists in the separation by gas of charged molecules, based on their mass-over-charge. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) first involves a separation by liquid chromatography (LC) followed by mass spectrometry in the MS and MS/MS modes.

ChromatographyLiquid chromatography–mass spectrometryChemistryBiomarker discoveryTandem mass spectrometryMass spectrometryWarping functionLabel free
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Recent trends in liquid chromatography-tandem mass spectrometry to determine pesticides and their metabolites in food

2007

Abstract The applications of liquid chromatography-mass spectrometry (LC-MS) have exploded in innumerable analytical fields, including pesticide-residue determination. There is no doubt that LC-MS is currently competing with gas chromatography (GC)-MS for the status of ‘reference’ analytical technique to determine pesticide residues and that its ever-increasing application is bound to the evolution of modern instruments and their growing performance qualities. We highlight the large number and variety of pesticides that can be readily determined using such instruments, the respective merits of the different mass analyzers, and the improvements brought about by tandem MS (MS 2 ). We also dis…

ChromatographyPesticide residueChemistryLiquid chromatography–mass spectrometryAnalytical techniqueGas chromatographyPesticideTandem mass spectrometryMass spectrometrySpectroscopyScreening proceduresAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Capabilities of different liquid chromatography tandem mass spectrometry systems in determining pesticide residues in food

2007

Abstract Three different liquid chromatography–mass spectrometry (LC–MS) instruments equipped with triple quadrupole (QqQ), quadrupole ion trap (QIT) and quadrupole-time-of-flight (QqTOF), suitable to carry out tandem mass spectrometry, were examined to determine pesticide residues in food. Twelve pesticides (acrinathrin, bupirimate, buprofezin, cyproconazole, λ-cyhalothrin, fluvalinate, hexaflumuron, kresoxim-methyl, propanil, pyrifenox, pyriproxyfen and tebufenpyrad) and six matrices (oranges, strawberries, cherries, peaches, apricots and pears) were taken as model. The comparison was focused on two aspects: the quantitative, covering sensitivity, precision and accuracy as well as the qua…

ChromatographyPesticide residueChemistryOrganic ChemistryBupirimateGeneral MedicineTandem mass spectrometryMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryTriple quadrupole mass spectrometerLiquid chromatography–mass spectrometryIon trapJournal of Chromatography A
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The Role of the Liquid Chromatography-Mass Spectrometry in Pesticide Residue Determination in Food

2008

The use of liquid chromatography (LC) in pesticide residue determination was usually limited to groups of compounds or single compounds for which no suitable gas chromatographic (GC) conditions were available. However, recent developments have significantly enlarged the LC scope in this field of analysis. One of the most important advances was the on-line coupling of efficient LC separation with mass spectrometry detectors (LC-MS and LC-MS/MS) that makes this technique an excellent method for the determination of pesticides and their transformation products in complex matrices such as food. This review considers the application of LC-MS/MS in this field. Emphasis is placed on the tandem MS …

ChromatographyPesticide residueLiquid chromatography–mass spectrometryChemistryAnalytical chemistryThermosprayDirect electron ionization liquid chromatography–mass spectrometry interfacePesticideTandem mass spectrometryMass spectrometrySample preparation in mass spectrometryAnalytical ChemistryCritical Reviews in Analytical Chemistry
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Target analysis of primary aromatic amines combined with a comprehensive screening of migrating substances in kitchen utensils by liquid chromatograp…

2015

An analytical strategy including both the quantitative target analysis of 8 regulated primary aromatic amines (PAAs), as well as a comprehensive post-run target screening of 77 migrating substances, was developed for nylon utensils, using liquid chromatography-orbitrap-high resolution mass spectrometry (LC-HRMS) operating in full scan mode. The accurate mass data were acquired with a resolving power of 50,000 FWHM (scan speed, 2 Hz), and by alternating two acquisition events, ESI+ with and without fragmentation. The target method was validated after statistical optimization of the main ionization and fragmentation parameters. The quantitative method presented appropriate performance to be u…

ChromatographyPrimary (chemistry)Food contactChemistryRelative standard deviationAnalytical chemistryTarget analysisFood ContaminationOrbitrapCooking and Eating UtensilsAnalytical Chemistrylaw.inventionMassNylonsKitchen utensilslawTandem Mass SpectrometryAnalytical strategyHumansAminesOrganic ChemicalsChromatography LiquidTalanta
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Multiresidue analysis of pesticides in honey by quechers and gas chromatography mass spectrometry in tandem

2011

ChromatographyTandemChemistryGeneral MedicineGas chromatography–mass spectrometryPesticideToxicologyQuechersToxicology Letters
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Genetic data of 10 X-STRs in a Spanish population sample

2007

In this work, we present population genetic data of 10 X-chromosome STRs (DXS8378, DXS9898, DXS8377, HPRTB, GATA172D05, DXS7423, DXS6809, DXS7132, DXS101 and DXS6789) obtained from sample of 145 unrelated female individuals belonging to Valencia (Spain), a region located in the east of the Iberian Peninsula. All the markers studied present high genetic diversities, similar to those previously reported in other European population samples. No deviations from Hardy-Weinberg equilibrium were observed, with the exception of DXS101 locus. Allele frequencies and parameters of forensic interest for each X-STR were calculated. High mean exclusion chance and power of discrimination values were obtai…

Chromosomes Human Xeducation.field_of_studyPopulationPopulation geneticsGenetic dataLocus (genetics)BiologyDNA FingerprintingPolymerase Chain ReactionhumanitiesPathology and Forensic MedicineSpanish populationExact testGenetics PopulationGene FrequencySpainTandem Repeat SequencesEvolutionary biologyHumansMicrosatelliteFemaleeducationLawAllele frequencyDemographyForensic Science International
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How copper ions and membrane environment influence the structure of the human and chicken tandem repeats domain?

2019

Abstract Prion proteins (PrPs) from different species have the enormous ability to anchor copper ions. The N-terminal domain of human prion protein (hPrP) contains four tandem repeats of the –PHGGGWGQ– octapeptide sequence. This octarepeat domain can bind up to four Cu2+ ions. Similarly to hPrP, chicken prion protein (chPrP) is able to interact with Cu2+ through the tandem hexapeptide -HNPGYP- region (residues 53–94). In this work, we focused on the human octapeptide repeat (human Octa4, hPrP60–91) (Ac-PHGGGWGQPHGGGWGQPHGGGWGQPHGGGWGQ-NH2) and chicken hexapeptide repeat (chicken Hexa4, chPrP54–77) (Ac-HNPGYPHNPGYPHNPGYPHNPGYP-NH2) prion protein fragments. Due to the fact that PrP is a membr…

Circular dichroism010402 general chemistry01 natural sciencesBiochemistryMicelleInorganic Chemistrychemistry.chemical_compoundMembrane LipidsTandem repeatPeptide bondAnimalsHumansAmino Acid SequenceSodium dodecyl sulfateLipid bilayerMembrane mimicking environmentMicelleschemistry.chemical_classification010405 organic chemistryChemistryCopper ionsSodium Dodecyl SulfateHistidine residues0104 chemical sciencesPrion proteinsMembraneTandem Repeat SequencesBiophysicsPotentiometryThermodynamicsGlycoproteinChickensCopper
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Separation, isolation and stereochemical assignment of imazalil enantiomers and their quantitation in an in vitro toxicity test

2016

A simple method for the separation of the enantiomers of the fungicide imazalil was developed. Racemic imazalil was separated into its enantiomers with an enantiomeric purity of 99% using HPLC-UV with an enantioselective column (permethylated cyclodextrin) operated in reversed phase mode (water with 0.2% trimethylamine and 0.08% acetic acid and methanol). The absolute configuration of the separated enantiomers was assigned and unequivocally confirmed by optical rotation as well as by vibrational circular dichroism (VCD) and electronic circular dichroism (ECD) combined with ab-initio calculations. The same enantioselective column was also used to develop an HPLC-MS/MS method for the quantifi…

Circular dichroismOptical RotationTrimethylamineIn Vitro Techniques010501 environmental sciencesTandem mass spectrometryVibration01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundTandem Mass SpectrometryToxicity TestsImazalil Enantiomers HPLC-UV Isolation Vibrational circular dichroism HPLC–MS/MSHumansChromatography High Pressure Liquid0105 earth and related environmental scienceschemistry.chemical_classificationChromatographyCyclodextrin010405 organic chemistryCircular DichroismOrganic ChemistryImidazolesAbsolute configurationEnantioselective synthesisStereoisomerismGeneral MedicineFungicides Industrial0104 chemical scienceschemistryVibrational circular dichroismSteroidsEnantiomerJournal of Chromatography A
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Strategies to In Vitro Assessment of Major Human CYP Enzyme Activities by Using Liquid Chromatography Tandem Mass Spectrometry

2008

At the early stage of drug discovery, thousands of new chemical entities (NCEs) may be screened before a single candidate can be identified for development. Determining the role of CYP enzymes in the metabolism of a compound and evaluating the effect of NCEs on human CYP activities are key issues in pharmaceutical development as they may explain inter-subject variability, drug-drug interactions, non-linear pharmacokinetics and toxic effects. Reliable methods for determining enzyme activities are needed to characterize an individual CYP enzyme and to obtain a tool for the evaluation of its role in drug metabolism in humans. Different liquid chromatography tandem mass spectrometry methodologi…

Clinical BiochemistryDrug Evaluation PreclinicalIn Vitro TechniquesTandem mass spectrometrySubstrate SpecificityCytochrome P-450 Enzyme SystemPharmacokineticsTandem Mass SpectrometryIn vivoLiquid chromatography–mass spectrometryCytochrome P-450 Enzyme InhibitorsHumansPharmacokineticsEnzyme inducerChromatography High Pressure LiquidCytochrome P-450 Enzyme InhibitorsPharmacologyChromatographybiologyDrug discoveryChemistryPharmaceutical PreparationsBiochemistryEnzyme InductionHepatocytesMicrosomes Liverbiology.proteinDrug metabolismCurrent Drug Metabolism
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