Search results for "performance"

showing 10 items of 4457 documents

Development and validation of RP-HPLC method for the quantitative estimation of αs1-genetic variants in goat milk

2013

A high-performance liquid chromatographic (HPLC) method was developed and validated for separation and quantification of the most common genetic variants of as1-casein in goat’s milk, to evaluate the effect of as1-casein polymorphisms on casein content. Chromatography was carried out by binary gradient technique on a reversed-phase C8 Zorbax column and the detection was made at a wavelength of 214 nm. The procedure was developed using individual raw milk samples of Girgentana goats. For calibration experiments, pure genetic variants were extracted from individual milk samples of animals with known genotypes, considering that commercial standards for goat genetic variants were not available.…

ChromatographyGenotypeGoatsGenetic variantsCaseinsGenetic VariationGeneral MedicineRaw milkBiologyHigh-performance liquid chromatographyGirgentana goat breedAnalytical ChemistryGenetic variants as1-Casein HPLC Goat milkSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoMilkCaseinGenotypeAnimalsFood scienceAlleleChromatography High Pressure LiquidFood ScienceFood Chemistry
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Determination of Phenols from Automobile Exhaust by Means of High-Performance Liquid Chromatography (HPLC)

1981

Abstract The paper describes a procedure to determine ten representative phenols (phenol, m-, p-, o-cresol, 2,4-, 2,6-, 3,4-, 3,5-xylenol, 2,3,6-, 2,4,6-trimethylphenol) in engine exhaust. Sampling was performed by a conventional Grimmer device. A sample of the water condensate collected was extracted with ether. After concentration of the ether extract phenols were isolated from other interfering compounds by stepwise elution on a Lobar column packed with LiChroprep Si 60 under controlled conditions. Relative recovery of the majority of reference phenols ranged from 90-100%. Separation of phenols into individual components was performed on polar packings as well as on Reverse Phase packing…

ChromatographyHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthAnalytical chemistrySoil ScienceEtherPollutionHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)Environmental ChemistryStepwise elutionPhenolPhenolsAcetonitrileWaste Management and DisposalQuantitative analysis (chemistry)Water Science and TechnologyInternational Journal of Environmental Analytical Chemistry
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High-performance liquid chromatographic determination of Maillard compounds in store-brand and name-brand ultra-high-temperature-treated cows' milk.

2000

Furosine and furfural products of the Maillard reaction are used as specific indicators of the effect of heating treatments on milk quality. Their contents were measured in representative samples of store- and name-brand ultra-high-temperature-treated milks using RP-HPLC with UV detection. Furosine contents ranged from 40.32 to 50.67 and from 65.48 to 310.58 mg/100 g protein in name- and store-brand milks, respectively. Of the furfurals, only hydroxymethylfurfural was detected. The free hydroxymethylfurfural contents of store-brand milks ranged from 0.22 to 1.70 mg/100 g protein. Total hydroxymethylfurfural contents ranged from 0.29 to 0.41 and from 0.72 to 2.21 mg/100 g protein, for name- …

ChromatographyHot TemperatureOrganic ChemistryFood composition dataGeneral MedicineReversed-phase chromatographyFurfuralBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMaillard Reactionchemistry.chemical_compoundMaillard reactionsymbols.namesakeMilkchemistrysymbolsAnimalsCattleSpectrophotometry UltravioletUv detectionQuantitative analysis (chemistry)HydroxymethylfurfuralChromatography High Pressure LiquidJournal of chromatography. A
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An automated on-line multidimensional HPLC system for protein and peptide mapping with integrated sample preparation.

2002

A comprehensive on-line two-dimensional 2D-HPLC system with integrated sample preparation was developed for the analysis of proteins and peptides with a molecular weight below 20 kDa. The system setup provided fast separations and high resolving power and is considered to be a complementary technique to 2D gel electrophoresis in proteomics. The on-line system reproducibly resolved approximately 1000 peaks within the total analysis time of 96 min and avoided sample losses by off-line sample handling. The low-molecular-weight target analytes were separated from the matrix using novel silica-based restricted access materials (RAM) with ion exchange functionalities. The size-selective sample fr…

ChromatographyIon exchangeChemistryIon chromatographyAnalytical chemistryProteinsUltrafiltrationFibroblastsMass spectrometryChromatography Ion ExchangeHigh-performance liquid chromatographyOnline SystemsPeptide MappingAnalytical ChemistryCell LineMatrix (chemical analysis)Matrix-assisted laser desorption/ionizationTwo-dimensional chromatographySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationHumansSample preparationElectrophoresis Polyacrylamide GelChromatography High Pressure LiquidAnalytical chemistry
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Pesticides (New Generation) and Related Compounds, Analysis of

2017

Miscellaneous pesticides and related compounds comprise substances that can neither be included in the classical chemical category of pesticides nor classified by their mode of action. They are a heterogeneous group of substances, the most representative of which are macrocyclic lactones, chloronicotinyls, tetranortriterpenoids, ammonium quaternary salts, dinitroanilines, acetamides, oximes, triazoles, and pyridine-based molecules. The pesticides covered in this article have hardly changed in the last years. However, their analytical determination has undergone significant improvements. This article provides a well-defined and critical compilation of the sample treatment and clean-up proced…

ChromatographyLiquid chromatography–mass spectrometryChemistryOrganic chemistrySample preparationGas chromatographySolid phase extractionGas chromatography–mass spectrometryPesticideMass spectrometryHigh-performance liquid chromatography
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Error analysis and performance of different retention models in the transference of data from/to isocratic/gradient elution.

2003

The transferability of retention data among isocratic and gradient RPLC elution modes is studied. For this purpose, 16 beta-blockers were chromatographed under both isocratic and gradient elution with acetonitrile-water mobile phases. Taking into account the elution mode where the experimental data come from, and the mode where the retention should be predicted, the following combinations are possible: isocratic predictions from (i) isocratic or (ii) gradient experimental designs; and gradient predictions from (iii) isocratic or (iv) gradient data. Each of these possibilities was checked using three retention models that relate the logarithm of the retention factor: (a) linearly and (b) qua…

ChromatographyLogarithmChemistryElutionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)Phase (matter)Volume fractionConfidence IntervalsGradient elutionChromatography LiquidJournal of chromatography. A
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Column technology in liquid chromatography

2017

This chapter deals with the most important part of the liquid chromatography (LC) system: the column enabling the efficient and fast resolution of complex mixtures. It is divided into seven sections under the overall aspects of manufacture, operation, and evaluation of analytical columns for the user. The first three sections highlight the column design and hardware, followed by a thorough treatment of the properties of microparticulate silica adsorbents as packing material, stationary phases performed by surface functionalization, and the column filling process. Then, the implementation of the column into the LC system is discussed, leading into chromatographic column testing as a C18-bond…

ChromatographyMaterials sciencePeriod (periodic table)Resolution (mass spectrometry)010401 analytical chemistrySilica column02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesColumn (database)High-performance liquid chromatography0104 chemical sciencesHighly sensitiveAdsorptionSurface modification0210 nano-technologyPorosityColumn design
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Modelling of retention behaviour of solutes in micellar liquid chromatography

1997

In micellar liquid chromatography (MLC), the resolution for a given multi-component mixture can be optimized by changing several variables, such as the concentrations of surfactant and organic modifier, the pH and temperature. However, this advantage can only be fully exploited with the development of mathematical models that describe the retention and the separation mechanisms. Several reports have appeared recently on the possibilities of accurately predicting the solute retention in MLC. Although the retention and selectivity may strongly change with varying concentrations of surfactant, organic modifier and/or pH, the observed changes are very regular, and are well described by simple m…

ChromatographyMathematical modelResolution (mass spectrometry)ChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPulmonary surfactantMicellar liquid chromatographyIonic strengthCritical micelle concentrationSelectivityJournal of Chromatography A
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Comparison of microextraction procedures to determine pesticides in oranges by liquid chromatography-mass spectrometry.

2002

A liquid chromatographic-mass spectrometric method has been developed for the determination of bitertanol, carbendazim, fenthion, flusilazole, hexythiazox, imidacloprid, methidathion, methiocarb, pyriproxyfen and trichlorfon. Two procedures, based on stir bar sorptive extraction (SBSE) and matrix solid-phase dispersion (MSPD), have been evaluated for the extraction of these compounds in oranges. Their respective advantages and disadvantages are also discussed. The recoveries obtained by MSPD ranged from 47 to 96% and the relative standard deviations (RSDs) ranged from 1 to 15%, whereas with the SBSE method the recoveries were between 8 and 84% and the RSDs between 4 and 16%. Although, the l…

ChromatographyMethiocarbCarbendazimOrganic ChemistryEthyl acetateReproducibility of ResultsGeneral MedicineMethidathionBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometrySample preparationSolid phase extractionPesticidesChromatography LiquidCitrus sinensisJournal of chromatography. A
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Homochiral Metal-Organic Frameworks for Enantioselective Separations in Liquid Chromatography

2020

Selective separation of enantiomers is a substantial challenge for the pharmaceutical industry. Chromatography on chiral stationary phases is the standard method, but at a very high cost for industrial-scale purification due to the high cost of the chiral stationary phases. Typically, these materials are poorly robust, expensive to manufacture, and often too specific for a single desired substrate, lacking desirable versatility across different chiral analytes. Here, we disclose a porous, robust homochiral metal–organic framework (MOF), TAMOF-1, built from copper(II) and an affordable linker prepared from natural l-histidine. TAMOF-1 has shown to be able to separate a variety of model…

ChromatographyMolecular StructureChemistryIndustrial scaleEnantioselective synthesisQuímica organometàl·licaWaterStereoisomerismStereoisomerismGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryHigh-performance liquid chromatography54Catalysis0104 chemical sciencesColloid and Surface ChemistryMoleculeWater chemistryMetal-organic frameworkEnantiomerChromatography High Pressure LiquidCopperMetal-Organic Frameworks
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