Search results for "Liquid Chromatography"

showing 10 items of 942 documents

Is multidimensional high performance liquid chromatography (HPLC) an alternative in protein analysis to 2D gel electrophoresis?

2000

The interactive modes of High Performance Liquid Chromatography (HPLC) of proteins provide a platform for the construction of a multidimensional HPLC system coupled to mass spectrometry. We present a system composed of both anion and cation exchanger columns, in the first dimension, and n-octadecyl bonded 1.5 μm nonporous silica columns in the second dimension. Both columns are operated under gradient conditions. A system suitability test with standard proteins showed that the total analysis can be performed within about 20 minutes. The fractions taken from the ion exchanger column are directly analyzed within one minute on the reversed phase column at a high flow rate. Two reversed phase c…

Chiral column chromatographychemistry.chemical_classificationChromatographyTwo-dimensional chromatographyChemistryGlobular proteinGeneral Chemical EngineeringIon chromatographyAnalytical chemistryReversed-phase chromatographyMass spectrometryChromatography columnHigh-performance liquid chromatography
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Modulation of the growth and metabolic response of cyanobacteria by the multifaceted activity of naringenin

2017

The interactions between the plant-derived bioflavonoid, naringenin, and prokaryotic microalgae representatives (cyanobacteria), were investigated with respect to its influence on the growth and metabolic response of these microorganisms. To achieve reliable results, the growth of cyanobacteria was determined based on measurements of chlorophyll content, morphological changes were assessed through microscopic observations, and the chemical response of cells was determined using liquid and gas chromatography (HPLC; GC-FID). The results show that micromolar levels of naringenin stimulated the growth of cyanobacteria. Increased growth was observed for halophilic strains at naringenin concentra…

ChlorophyllPigments0301 basic medicineCyanobacteriaNaringeninExopolysaccharidesChloroplastsMicroorganismCellGlycobiologyMarine and Aquatic Scienceslcsh:MedicineFresh WaterPlant ScienceBiochemistrychemistry.chemical_compoundElectron MicroscopyNostoclcsh:ScienceLiquid ChromatographyMicroscopyMultidisciplinarybiologyChemistryChromatographic Techniquesfood and beveragesHalophilemedicine.anatomical_structureBiochemistryFlavanonesPhysical SciencesScanning Electron MicroscopyCellular Structures and OrganellesCellular TypesResearch ArticleFreshwater EnvironmentsChromatography GasPlant Cell BiologyMaterials Science030106 microbiologyCyanobacteriaResearch and Analysis MethodsCell wallExcretion03 medical and health sciencesPolysaccharidesPlant CellsmedicineMaterials by AttributeBacteriaOrganic PigmentsEcology and Environmental Scienceslcsh:ROrganismsBiology and Life SciencesAquatic EnvironmentsCell Biologybiology.organism_classificationAnabaenaHigh Performance Liquid Chromatography030104 developmental biologyEarth Scienceslcsh:QBacteriaChromatography LiquidNostoc muscorumPLOS ONE
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Microscale synthesis of phosphatidyl-[3H]choline from 1,2-diacylglycerol. Assessment of isomerization by reversed-phase high-performance liquid chrom…

1995

The synthesis of rac-1-palmitoyl-2-oleoylglycero-3-phospho-[3H]choline of high specific activity was carried out on a microscale by making 7 mumol of rac-1-palmitoyl-2-oleoylglycerol react first with an equimolar amount of POCl3 and then of [3H]choline. After purification by thin-layer chromatography and normal-phase high-performance liquid chromatography and normal-phase high-performance liquid chromatography (HPLC), the yield of the synthesis of [3H]phosphatidylcholine (120 microCi/mumol) was 22%. rac-1-Palmitoyl-2-oleoylglycerol was purified before use by reversed-phase HPLC under conditions which were nonisomerizing and allowed the separation of 1,2- and 1,3-isomers of diacylglycerol. E…

Chromatography GasChromatographyOrganic ChemistryStereoisomerismCell BiologyReference StandardsBiochemistryHigh-performance liquid chromatographyDiglycerideschemistry.chemical_compoundchemistryPhosphatidylcholinePhosphatidylcholinesCholineChromatography Thin LayerMethanolAcetonitrileIsomerizationChromatography High Pressure LiquidCholine chlorideDiacylglycerol kinaseLipids
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Analysis of eicosapentaenoic and docosahexaenoic acid geometrical isomers formed during fish oil deodorization.

2006

International audience; Addition of long-chain polyunsaturated fatty acids (LC-PUFAs) from marine oil into food products implies preliminary refining procedures of the oil which thermal process affects the integrity of LC-PUFAs. Deodorization, the major step involving high temperatures, is a common process used for the refining of edible fats and oils. The present study evaluates the effect of deodorization temperature on the formation of LC-PUFA geometrical isomers. Chemically isomerized eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) were used as reference samples. Fish oil samples have been deodorized at 180, 220 and 250 °C for 3 h and pure EPA and DHA fatty acid methyl esters…

Chromatography GasHot TemperatureDocosahexaenoic Acids[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process Engineering030309 nutrition & dietetics01 natural sciencesBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySILVER-ION CHROMATOGRAPHY03 medical and health sciencesFish OilsIsomerismDECOSAHEXAENOIC ACID[SDV.IDA]Life Sciences [q-bio]/Food engineeringOrganic chemistry[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringChromatography High Pressure Liquidchemistry.chemical_classificationFlame IonizationFISH OIL0303 health sciencesChromatographyChemistry010401 analytical chemistryOrganic ChemistryFatty acidReproducibility of ResultsGeneral Medicine[SDV.IDA] Life Sciences [q-bio]/Food engineeringFish oilEicosapentaenoic acidTRANS FATTY ACIDS0104 chemical sciencesEicosapentaenoic Acid13. Climate actionDocosahexaenoic acidDEODORIZATIONOdorantsFatty Acids Unsaturatedlipids (amino acids peptides and proteins)Gas chromatographyChromatography Thin LayerIsomerizationCis–trans isomerismTolueneJournal of chromatography. A
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Performance of short-chain alcohols versus acetonitrile in the surfactant-mediated reversed-phase liquid chromatographic separation of β-blockers

2010

Organic solvents are traditionally added to micellar mobile phases to achieve adequate retention times and peak profiles, in a chromatographic mode which has been called micellar liquid chromatography (MLC). The organic solvent content is limited to preserve the formation of micelles. However, at increasing organic solvent contents, the transition to a situation where micelles do not exist is gradual. Also, there is no reason to neglect the potentiality of mobile phases containing only surfactant monomers instead of micelles (high submicellar chromatography, HSC). This is demonstrated here for the analysis of β-blockers. The performance of four organic solvents (methanol, ethanol, 1-propano…

Chromatography Reverse-PhaseAcetonitrilesChromatographyElutionAdrenergic beta-AntagonistsOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyMicelleAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundModels ChemicalchemistryPulmonary surfactantMicellar liquid chromatographyAlcoholsData Interpretation StatisticalMethanolAcetonitrileAlgorithmsMicellesJournal of Chromatography A
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Comparison of surfactant-mediated liquid chromatographic modes with sodium dodecyl sulphate for the analysis of basic drugs

2020

In reversed-phase liquid chromatography (RPLC), basic drugs are positively charged at the usual working pH range and interact with free anionic silanols present in conventional silica-based stationary phases. This translates into stronger retention and tailed and broadened peaks. This problem can be resolved by the addition of reagents to the mobile phase that are adsorbed on the stationary phase, avoiding the access of solutes to silanols. Among these additives, surfactants under micellar conditions have provided good silanol suppressing potency through the technique known as micellar liquid chromatography (MLC). The most common example of this is anionic sodium dodecyl sulphate (SDS). Whe…

Chromatography Reverse-PhaseAqueous solutionChromatographyChemistryGeneral Chemical Engineering010401 analytical chemistryGeneral EngineeringSodium Dodecyl Sulfate02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMicelle0104 chemical sciencesAnalytical ChemistrySurface-Active AgentsSilanolchemistry.chemical_compoundPulmonary surfactantMicellar liquid chromatographyReagentPhase (matter)Microemulsion0210 nano-technologyMicellesChromatography LiquidAnalytical Methods
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Implementation of gradients of organic solvent in micellar liquid chromatography using DryLab®: Separation of basic compounds in urine samples

2014

In micellar liquid chromatography (MLC), chromatographic peaks are more evenly distributed compared to conventional reversed-phase liquid chromatography (RPLC). This is the reason that most procedures are implemented using isocratic elution. However, gradient elution may be still useful in MLC to analyse mixtures of compounds within a wide range of polarities, decreasing the analysis time. Also, it benefits the determination of moderately to low polar compounds in physiological fluids performing direct injection: an initial micellar eluent with a low organic solvent content, or a pure micellar (without surfactant) solution, will provide better protection of the column against the proteins i…

Chromatography Reverse-PhaseChromatographyChemistryElutionChemical polarityAdrenergic beta-AntagonistsOrganic ChemistryAnalytical chemistryGeneral MedicineBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compound1-PropanolColumn chromatographyPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationSolventsHumansIndicators and ReagentsAnalytical proceduresMicellesSoftwareJournal of Chromatography A
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Review: Determination of Vitamin D in Dairy Products by High Performance Liquid Chromatography

2005

This work reviews the methods used for the determination of vitamin D in some dairy products (milk and infant formulas) by high performance liquid chromatography (HPLC). The low vitamin D contents and the presence of interfering compounds require sample treatment and purification of the extract. The advantages and drawbacks of hot and cold saponification, direct extraction and different types of extract purification are also discussed, taking into account the lack of vitamin D stability by heating, exposure to light and oxidation. With respect to chromatographic determination, the mode (normal or reverse phase), type of column (microcolumn or conventional) and detection system (UV, electro…

Chromatography010405 organic chemistryChemistryGeneral Chemical Engineering010401 analytical chemistryExtraction (chemistry)Vitamina dMass spectrometry01 natural sciencesHigh-performance liquid chromatographyIndustrial and Manufacturing Engineering0104 chemical sciencesInfant formulaBy-productVitamin D and neurologySaponificationFood ScienceFood Science and Technology International
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Eucalyptol-based green extraction of brown alga Zonaria tournefortii

2018

Abstract A green extraction method, based on the use of 1,8-cineole (eucalyptol) as biosolvent, has been developed to prepare crude extracts from the brown alga Zonaria tournefortii characterized by chemical composition, particularly dominated by phenolic compounds derived from phloroglucinol. The main advantage of the developed technique are the recovery of eucalyptol, based on multistep liquid-liquid extraction with distilled water, followed by centrifugation and elimination of the aqueous phase, and the complete recycling of biosolvent by steam distillation. A comparative study between the proposed green extract and the conventional extract, prepared by solvent maceration using the mixtu…

Chromatography010405 organic chemistryDPPH010401 analytical chemistryExtraction (chemistry)Aqueous two-phase systemPharmaceutical ScienceManagement Monitoring Policy and Law01 natural sciencesPollutionHigh-performance liquid chromatography0104 chemical scienceslaw.inventionSteam distillationchemistry.chemical_compoundEucalyptolchemistrylawMaceration (wine)Environmental ChemistryPhenolsSustainable Chemistry and Pharmacy
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Comparison of photodiode array, evaporative light scattering, and single-quadrupole mass spectrometric detection methods for the UPLC analysis of pyr…

2017

ABSTRACTIt is important to analyze pyrolysis liquids to evaluate the yield of valuable products as well as unfavorable by-products. This work focuses on choosing detectors for reversed-phase ultra high-performance liquid chromatography analysis of pyrolysis liquids. The linearity, sensitivity, precision, and recovery of photodiode array (PDA) detector, single-quadrupole mass spectrometer (MS), and evaporative light scattering (ELS) detector were compared for the quantitative determination of several typical compounds found in pyrolysis liquids. PDA and MS detectors were found to be suitable for the quantification of furans and phenol derivatives (furfural, vanillin, syringol), but sugars an…

Chromatography010405 organic chemistryLevoglucosan010401 analytical chemistryClinical BiochemistrySyringolAnalytical chemistryPharmaceutical ScienceMass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyLight scattering0104 chemical sciencesAnalytical ChemistryPhotodiodelaw.inventionchemistry.chemical_compoundchemistryChromatography detectorlawPyrolysisJournal of Liquid Chromatography & Related Technologies
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