Search results for "FRACTIONATION"

showing 10 items of 332 documents

Sample preparation methods for the determination of pesticides in foods using CE-UV/MS.

2010

Much progress has been made in pesticide analysis over the past decade, during this time hyphenated techniques involving highly efficient separation with sensitive detection have become the techniques of choice. Among these, methods based on separation with mass spectrometric detection have resulted in greater likelihood of identification and are acknowledged to be extremely useful and authoritative methods for the determination of pesticide residues but the inherent advantages of the use of CE as a separation technique are well-known and can be summarized as high separation efficiency, low analysis time, high resolution power, and low consumption of samples and reagents. Although UV is the…

ChromatographyPesticide residueChemistryClinical BiochemistryHigh resolutionElectrophoresis CapillaryLimitingPesticideChemical FractionationMicrofluidic Analytical TechniquesBiochemistryMass spectrometricFood AnalysisMass SpectrometryAnalytical ChemistryCapillary electrophoresisSample preparationSpectrophotometry UltravioletBiochemical engineeringPesticidesFood AnalysisElectrophoresis
researchProduct

Large scale fractionation of pullulan and dextran

2006

Abstract A recently developed large scale fractionation technique named continuous spin fractionation (CSF) was applied to fractionate pullulan and dextran. 450 g of pullulan with a broad molecular weight distribution were fractionated using water as solvent and acetone as precipitant. In this study, we have in five CSF runs prepared three fractions with apparent M ¯ w * values ranging from 17.6 to 413 kg mol−1. Seventy grams of dextran were fractionated with a mixed solvent of water plus methanol. Five fractionation steps resulted in four samples with M ¯ w values between 4.36 and 18.2 kg mol−1.

ChromatographyPolymers and PlasticsOrganic ChemistryPullulanFractionationSolventchemistry.chemical_compoundDextranchemistryPhysical separationMaterials ChemistryAcetoneMolar mass distributionMethanolCarbohydrate Polymers
researchProduct

Packings and stationary phases for biopolymer separations by HPLC

1987

Packings and stationary phases applied to high resolution separations of proteins, enzymes, and nucleic acids must satisfy a series of distinct criteria that are different from those usually required by HPLC of low molecular weight non-biologically active analytes. These requirements have been met through substantial improvements in classical gel media together with novel developments in silica supports, and have led to a family of products with tailor-made and reproducible properties. Supports consisting of cross-linked organic gels, and inorganic materials (mostly silicas) are now available with graduated particle sizes, pore sizes, porosities and surface areas as well as non-porous beads…

ChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryClinical BiochemistrySize-exclusion chromatographyFractionationengineering.materialBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectPhase (matter)Protein purificationengineeringBiopolymerChromatographia
researchProduct

Influence of oscillating main flow on separation efficiency in asymmetrical flow field-flow fractionation.

2021

The steadily rising interest in the investigation of interactions between nanomaterials and biological media has also led to an increasing interest in asymmetrical flow field-flow fractionation (AF-FFF). The biggest strength of AF-FFF is the possibility to alter the flow profiles to suit a specific separation problem. In this paper, the influence of an oscillating main flow on the separation efficiency of AF-FFF is investigated. Such oscillations can e.g. be caused by the main pump To investigate the influence of such flow conditions on the separation efficiency in AF-FFF systematically, different oscillation profiles were applied and their influence on the elution profile and the retention…

ChromatographyTime FactorsFourier AnalysisElutionOscillationChemistryAsymmetrical Flow Field-Flow Fractionation010401 analytical chemistryOrganic ChemistryFlow (psychology)Separation (aeronautics)General MedicineFractionationMechanicsReference Standards010402 general chemistry01 natural sciencesBiochemistryFractionation Field Flow0104 chemical sciencesAnalytical ChemistryFlow conditionsPolystyrenesRheologySeparation problemJournal of chromatography. A
researchProduct

Use of an enzyme-assisted method to improve protein extraction from olive leaves.

2013

The improvement of protein extraction from olive leaves using an enzyme-assisted protocol has been investigated. Using a cellulase enzyme (Celluclast® 1.5L), different parameters that affect the extraction process, such as the influence and amount of organic solvent, enzyme amount, pH and extraction temperature and time, were optimised. The influence of these factors was examined using the standard Bradford assay and the extracted proteins were characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The optimum extraction parameters were: 30% acetonitrile, 5% (v/v) Celluclast® 1.5L at pH 5.0 and 55°C for 15min. Under these conditions, several protein extracts…

ChromatographybiologyChemistryPlant ExtractsSodiumExtraction (chemistry)Temperaturechemistry.chemical_elementGeneral MedicineCellulaseChemical FractionationAnalytical ChemistrySolventPlant LeavesElectrophoresisCellulaseOleaProtein purificationbiology.proteinElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisBradford protein assayFood SciencePlant ProteinsFood chemistry
researchProduct

Enzymatic cleaning of inorganic ultrafiltration membranes used for whey protein fractionation

2003

Abstract The aim of this work was to study the cleaning of inorganic membranes fouled by whey protein solutions using proteolytic enzymes. Tami ® 150+4T membranes (Tami Industries, S.A., 26110 Nyons, France) of 400 kg/mol molecular weight cut-off (MWCO) and a ZrO 2 filtering layer were selected to carry out the tests and Maxatase ® XL (Genencor International, 2333 CN Leiden, The Netherlands) and P3-Ultrasil ® 62 (Henkel Iberica, S.A., 08025 Barcelona, Spain) were investigated as cleaning agents. Cleaning efficiency was observed to be a function of the operating conditions. The operating conditions studied were the pH of the cleaning solution, the enzymatic agent concentration and cleaning t…

Cleaning agentWhey proteinChromatographyChemistryUltrafiltrationProteolytic enzymesFiltration and SeparationFractionationPermeationBiochemistryHydrolysisMembraneGeneral Materials SciencePhysical and Theoretical ChemistryJournal of Membrane Science
researchProduct

Portable microwave assisted extraction: An original concept for green analytical chemistry.

2013

International audience; This paper describes a portable microwave assisted extraction apparatus (PMAE) for extraction of bioac-tive compounds especially essential oils and aromas directly in a crop or in a forest. The developed procedure, based on the concept of green analytical chemistry, is appropriate to obtain direct in-field information about the level of essential oils in natural samples and to illustrate green chemical lesson and research. The efficiency of this experiment was validated for the extraction of essential oil of rosemary directly in a crop and allows obtaining a quantitative information on the content of essential oil, which was similar to that obtained by conventional m…

Crops Agricultural[SDV]Life Sciences [q-bio]Analytical chemistrychromatographie en phase gazeusechimie verteExtraction02 engineering and technologyChemical Fractionation01 natural sciencesBiochemistryMicrowave assistedEssential oilAnalytical Chemistrylaw.inventionrosmarinus officinalislawOils Volatilehuile essentielleMicrowavesEssential oilcomposition aromatiqueChromatographyMiniaturizationPortable microwave assisted extractionChemistryPlant ExtractsGreen analytical chemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Portable microwave assisted extraction;Miniaturization;Green analytical chemistry;Extraction;Essential oilmicroondefood and beveragesGreen Chemistry TechnologyGeneral Medicineextraction d'huile021001 nanoscience & nanotechnologyRosmarinus0104 chemical sciences0210 nano-technology
researchProduct

Structure of the Cryptosporidium parvum microneme: a metabolically and osmotically labile apicomplexan organelle.

2003

From an EM study of thin sections, the rod-like microneme organelles within conventionally glutaraldehyde fixed Cryptosporidium parvum sporozoites have been shown to undergo a shape change to a more spherical structure when the sporozoites age in vitro for a period of approximately 12 to 24 h. This correlates with the shape change of intact sporozoites, from motile hence viable thin banana-shaped cells to swollen pear-shaped cells, shown by differential interference contrast light microscopy of unstained unfixed and glutaraldehyde-fixed samples, as well as by thin section EM of fixed sporozoites. From negatively stained EM specimens of unfixed and fixed sporozoites the cellular shape change…

Cryptosporidium parvumOrganellesOsmosisCryoelectron MicroscopyOocystsGeneral Physics and AstronomyCell BiologyBiologybiology.organism_classificationCell FractionationNegative stainMicrobiologyCell biologyStainingMicronemeApicomplexaCryptosporidium parvumDifferential interference contrast microscopyStructural BiologyOrganelleUltrastructureAnimalsGeneral Materials ScienceCattlesense organsMicron (Oxford, England : 1993)
researchProduct

Ultrastructure, fractionation and biochemical analysis of Cryptosporidium parvum sporozoites.

1999

Abstract Sporozoites of the apicomplexan parasite Cryptosporidium parvum were subjected to cell disruption and subcellular fractionation using a sucrose density step gradient. With this procedure, highly enriched preparations of the parasite membrane, the micronemes, dense granules and amylopectin granules were produced. No separate fraction containing rhoptries was obtained, however this organelle was found in defined fractions of the gradient, still associated with the apical tip of the sporozoites. Using negative staining, the internal structure of the micronemes was revealed by transmission electron microscopy. Micronemes and dense granules showed characteristic protein compositions by …

Cryptosporidium parvumOrganellesRhoptryProtozoan ProteinsCattle DiseasesCryptosporidiosisBiologybiology.organism_classificationCell FractionationNegative stainApicomplexaMicronemeMicroscopy ElectronInfectious DiseasesCryptosporidium parvumBiochemistryOrganelleUltrastructureCentrifugation Density GradientAnimalsParasitologyCattleElectrophoresis Polyacrylamide GelCell fractionationInternational journal for parasitology
researchProduct

Small changes in particle-size distribution dramatically delay and enhance nucleation in hard sphere colloidal suspensions.

2006

We present hard-sphere crystallization kinetics for three samples with small differences in polydispersity. We show that an increase in polydispersity of 1% is sufficient to cause dramatic changes in the crystallization kinetics: Crystallization is delayed by almost one decade in time and quantitative and qualitative changes in the crystallization scenario are observed. Surprisingly the nucleation rate density is enhanced by almost a factor of 10. We interpret these results in terms of polydispersity limited growth, where local fractionation processes lead to a delayed but faster nucleation.

Crystallization kineticsColloidMaterials scienceChemical physicslawDispersityParticle-size distributionNucleationFractionationParticle sizeCrystallizationlaw.inventionPhysical review. E, Statistical, nonlinear, and soft matter physics
researchProduct