Search results for "Chemical analysis."

showing 10 items of 308 documents

Biodegradable tablets having a matrix of low molecular weight poly-L-lactic acid and poly-D,L-lactic acid.

1990

Biodegradable Homo- and Copolymers of lactic and glycolic acids have been used for manufacture of microparticles and matrix implants1,5). To ensure sufficient hydrolytic matrix stability lactic acids of high and medium degree of polymerization have been used. The manufacture of poly lactic acid tablets with an average molecular weight of 25000 and 6000 was reported recently, after finishing the following study2). Bioabbaubare Gerusttabletten aus niedermolekularer poly-L-Milchsaure und poly-D,L-Milchsaure

Poly l lactic acidChemistryPolymersMatrix stabilityPolyestersPharmaceutical ScienceStereoisomerismDegree of polymerizationLactic acidMatrix (chemical analysis)Molecular WeightHydrolysischemistry.chemical_compoundDrug DiscoveryCopolymerLactatesMolar mass distributionOrganic chemistryLactic AcidBiotransformationTabletsArchiv der Pharmazie
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Highly selective and sensitive chromo-fluorogenic detection of the Tetryl explosive using functional silica nanoparticles

2011

Silica nanoparticles containing polyamines and thiol groups have been used as probes for the selective detection of Tetryl. © 2011 The Royal Society of Chemistry.

PolyamineINGENIERIA DE LA CONSTRUCCIONUnclassified drugNanoparticlePhotochemistryColorimetry (chemical method)Nitrobenzenechemistry.chemical_compoundNanoparticleQUIMICA ORGANICAChemical structureSilicon dioxidePolyaminesMaterials ChemistryChemical analysischemistry.chemical_classificationAniline CompoundsChemistryMetals and Alloysrespiratory systemTetrylSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsThiolColorimetryDyeExplosive materialSilicon dioxideChemical structureArticleCatalysisThiol groupBinding site246 trinitrophenylmethylnitramineExplosive AgentsExplosiveReaction analysisQUIMICA ANALITICASulfhydryl CompoundsNitrobenzenesSensorFluorescent DyesFluorescent dyeQUIMICA INORGANICAGeneral ChemistrySilane derivativeCombinatorial chemistryChromogenic substrateCeramics and CompositesNanoparticlesChemical Communications
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Aroma behaviour during steam cooking within a potato starch-based model matrix.

2012

To help understand the organoleptic qualities of steam cooked foods, the kinetics of aroma release during cooking in a potato starch based model matrix was studied. Behaviour of components having a major impact in potato flavour were studied using solid phase micro extraction-gas chromatography (SPME-GC). Evolution of microstructure of potato starch model-matrix during steam cooking process was analyzed using environmental scanning electron microscopy (ESEM). Both aroma compounds that are naturally present in starch matrix and those that were added were analyzed. Both the aroma compounds naturally presented and those added had different behaviour depending on their physico-chemical properti…

Polymers and PlasticsbiologyChemistryStarchOrganic ChemistryFlavourOrganolepticfood and beveragesStarchbiology.organism_classificationMatrix (chemical analysis)chemistry.chemical_compoundStarch gelatinizationSteamOdorantsMaterials Chemistrypotato starch; steam cooking; aroma compounds; aromatization; mMicrostructural changesMicroscopy Electron ScanningOrganic chemistryFood scienceCookingEnvironmental scanning electron microscopePotato starchAromaSolanum tuberosumCarbohydrate polymers
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New background correction approach based on polynomial regressions for on-line liquid chromatography-Fourier transform infrared spectrometry.

2008

Abstract In the present study a new approach for the chemometric background correction in on-line gradient LC–FTIR is introduced. For this purpose, the spectral changes of the elution mixture during gradient elution were analyzed applying 2D correlation spectroscopy. The fundamentals of the new background correction algorithm, based on polynomial fits calculated from a reference spectra matrix (Polyfit-RSM method) are explained. The Polyfit-RSM approach was applied on blank gradient runs as well as on LC–FTIR data obtained from the injection of a soft drink sample using acetonitrile:water as eluent. Results found were critically assessed and compared to those obtained by two previous backgr…

PolynomialAnalyteChromatographyAcetonitrilesElutionChemistryOrganic ChemistryWaterGeneral MedicineBiochemistryNoise (electronics)Spectral lineAnalytical ChemistryMatrix (chemical analysis)BeveragesLine (geometry)Spectroscopy Fourier Transform InfraredRange (statistics)Regression AnalysisLeast-Squares AnalysisAlgorithmsChromatography High Pressure LiquidJournal of chromatography. A
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Protein Thermal Denaturation and Matrix Glass Transition in Different Protein−Trehalose−Water Systems

2011

Biopreservation by saccharides is a widely studied issue due to its scientific and technological importance; in particular, ternary amorphous protein-saccharide-water systems are extensively exploited to model the characteristics of the in vivo biopreservation process. We present here a differential scanning calorimetry (DSC) study on amorphous trehalose-water systems with embedded different proteins (myoglobin, lysozyme, BSA, hemoglobin), which differ for charge, surface, and volume properties. In our study, the protein/trehalose molar ratio is kept constant at 1/40, while the water/sugar molar ratio is varied between 2 and 300; results are compared with those obtained for binary trehalose…

Protein DenaturationdenaturationMolecular Dynamics SimulationPhase TransitionDSCMatrix (chemical analysis)Hemoglobinschemistry.chemical_compoundDifferential scanning calorimetryMaterials ChemistryAnimalsglass transitionPhysical and Theoretical ChemistrytrehaloseSettore CHIM/02 - Chimica FisicaChromatographyCalorimetry Differential ScanningMyoglobinTemperatureProteinsWaterSerum Albumin BovineTrehaloseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Surfaces Coatings and FilmsAmorphous solidchemistryChemical engineeringMyoglobinconfinementCattleMuramidaseLysozymeTernary operationGlass transitionThe Journal of Physical Chemistry B
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Metaproteomic analysis of atmospheric aerosol samples.

2016

Metaproteomic analysis of air particulate matter provides information about the abundance and properties of bioaerosols in the atmosphere and their influence on climate and public health. We developed and applied efficient methods for the extraction and analysis of proteins from glass fiber filter samples of total, coarse, and fine particulate matter. Size exclusion chromatography was applied to remove matrix components, and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was applied for protein fractionation according to molecular size, followed by in-gel digestion and LC-MS/MS analysis of peptides using a hybrid Quadrupole-Orbitrap MS. Maxquant software and the Swiss-…

Proteomics010504 meteorology & atmospheric sciencesSize-exclusion chromatographyIndoor bioaerosolFractionation010501 environmental sciences01 natural sciencesBiochemistryAnalytical ChemistryMatrix (chemical analysis)Fungal ProteinsBacterial ProteinsMetaproteomicsTandem Mass SpectrometryDatabases ProteinChromatography High Pressure Liquid0105 earth and related environmental sciencesPlant ProteinsAerosolsFungal proteinAir PollutantsChromatographyMass spectrometryChemistryAtmosphereProteinsParticulatesAllergensAtmospheric aerosolsAerosolEnvironmental chemistryBioanalytical methodsParticleElectrophoresis Polyacrylamide GelParticulate MatterHPLCResearch PaperAnalytical and bioanalytical chemistry
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Analysis of mycotoxins in barley using ultra high liquid chromatography high resolution mass spectrometry: comparison of efficiency and efficacy of d…

2012

The effectiveness of four extraction methods (modified QuEChERS, matrix solid-phase dispersion (MSPD), solid-liquid extraction (SLE) and solid-phase extraction (SPE) clean-up) were evaluated for simultaneous determination of 32 mycotoxins produced by the genus Fusarium, Claviceps, Aspergillus, Penicillium and Alternaria in barley by ultra high pressure liquid chromatography coupled to ultra-high resolution mass spectrometry (UHPLC-Orbitrap(®) MS). The efficiency and efficacy of extraction methods were evaluated and compared in number of extracted mycotoxins and obtained recoveries. From the one point of view, QuEChERS procedure was fast and easy, as well as it was able to successfully extra…

QuEChERSTime FactorsFood ContaminationChemical FractionationMass spectrometryOrbitrapQuechersMass SpectrometryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundlawMSPDSolid phase extractionMycotoxinChromatography High Pressure LiquidChromatographybiologyChemistryExtraction (chemistry)Reproducibility of ResultsHordeumSolid-liquid extractionClean-upMycotoxinsbiology.organism_classificationOrbitrapPenicilliumTalanta
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Control of matrix interferences by the multiple linear regression model in the determination of arsenic, antimony and tin in lead pellets by inductiv…

2002

A multiple linear regression technique was used to evaluate the matrix interferences in the determination of hydride-forming elements in lead shotgun pellets by inductively coupled plasma atomic emission spectrometry. The determination of arsenic, antimony, and tin in SRM C2416 (Bullet Lead) by ICP-AES failed to obtain the certified concentrations at the 95% level of confidence using the t-test. However, it proved possible, by using the multiple linear regression technique, to correct the concentrations of all three elements to a statistically acceptable level. This method of correction is based on the multiple regression line obtained from the analysis of 19 synthetic mixtures of matrix el…

RadiochemistryAnalytical chemistrychemistry.chemical_elementequipment and suppliesCopperAnalytical ChemistryBismuthMatrix (chemical analysis)chemistryAntimonyLinear regressionInductively coupled plasmaTinSpectroscopyArsenicJ. Anal. At. Spectrom.
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Electrochemical characterization of mangrove sediments: A proposal of new proxies for organic matter oxidation

2019

Abstract The voltammetric response of microparticulate deposits resulting from solvent evaporation of ethanolic extracts of mangrove sediments in contact with aqueous acetate buffer is hereby described. Dated sediment cores sampled from the Peruvian mangrove system (“Manglares de Tumbes” National Sanctuary) presented voltammetric responses dominated by oxidative signals of organic components that exhibit significant variations depending on the depth. Voltammetric data allowed for the definition of electrochemical indexes representative of the electrochemically oxidable organic matter fraction. These electrochemical indexes were fEAOM (for the total amount of organic matter being electrochem…

Redox state010501 environmental sciences010502 geochemistry & geophysicsElectrochemistryMangrove sediments01 natural sciencesevaporationPeruElectrochemistryChemical analysisInfrared spectroscopyorganic matterchemistry.chemical_classificationAqueous solutionChemistryBiogeochemistryPollutionOrganic matter oxidationEnvironmental chemistryOrganic matter degradationsMangroveoxidationInfrared spectroscopyredox conditionssolventSedimentsVoltammetric responseGeochemistry and PetrologyOrganic compoundsOrganic matter fractionEnvironmental ChemistryOrganic matter14. Life underwaterSpectroscopyOxidation proxies0105 earth and related environmental sciencesparticulate mattermangrove//purl.org/pe-repo/ocde/ford#1.05.00 [https]SedimentBiological materials15. Life on landcoastal sedimentElectrochemical characterizationssediment coreSolvent evaporationVoltammetryethanolacetateaqueous solutionReactive oxygen species
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An effective negative pressure cavitation-microwave assisted extraction for determination of phenolic compounds in P. calliantha H. Andr.

2013

A novel negative pressure and microwave assisted extraction technique (NMAE) was first proposed and applied for extraction of phenolic compounds from pyrola. [C₄MIM]BF₄ aqueous solution was selected as extraction solvent. Optimal extraction conditions were microwave power 700 W, negative pressure -0.07 MPa, temperature 40 °C, liquid-solid ratio 20 : 1, ionic liquid (IL) concentration 0.5 M, extraction time 15 min. The predominance of NMAE was investigated by comparing with microwave-assisted extraction (MAE) and negative pressure cavitation extraction (NPCE) using a first-order kinetics equation. The C∞ values of the target compounds by NMAE were from 0.406 to 5.977 mg g⁻¹ higher than these…

ReproducibilityAqueous solutionChromatographyPlant ExtractsLiquid-Liquid ExtractionExtraction (chemistry)Analytical chemistryRepeatabilityBiochemistryAnalytical ChemistrySolventMatrix (chemical analysis)chemistry.chemical_compoundPhenolschemistryIonic liquidPressureElectrochemistryEnvironmental ChemistrySample preparationMicrowavesPyrolaChromatography High Pressure LiquidSpectroscopyThe Analyst
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