Search results for "Kinetics"

showing 10 items of 2224 documents

Molecular organization via ionic interactions at interfaces. 1. Monolayers and LB films of cyclic bisbipyridinium tetracations and dimyristoylphospha…

1993

ChromatographyAqueous solutionChemical structureKineticsPhospholipidIonic bondingSurfaces and InterfacesCondensed Matter PhysicsSurface pressurechemistry.chemical_compoundchemistryChemical engineeringMonolayerElectrochemistryDimyristoylphosphatidic acidGeneral Materials ScienceSpectroscopyLangmuir
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Resin adsorption as a means to enrich rare stilbenes and coumarin from pigeon pea leaves extracts

2011

Abstract In this study, resin adsorption as a means to enrich rare stilbenes cajaninstilbene acid (CSA) and longistyline C (LLC), and coumarin cajanuslactone (CL) from pigeon pea leaves was investigated. Among widely used twenty macroporous adsorption resins, NKA-9 resin presented higher adsorption capacity and desorption ratio in static tests. The adsorption kinetic model fitted better depended on types of compounds and pH values. The experimental adsorption data were better fitted to Langmuir isotherm (R2 0.921–0.991) than Freundlich isotherm (R2 0.753–0.988). In order to optimize the operating parameters for separating CSA, LLC and CL, dynamic adsorption and desorption tests were carried…

ChromatographyCajaninstilbene acidChemistryGeneral Chemical EngineeringLangmuir adsorption modelGeneral ChemistryCoumarinIndustrial and Manufacturing Engineeringsymbols.namesakechemistry.chemical_compoundAdsorptionAdsorption kineticsDesorptionsymbolsEnvironmental ChemistryFreundlich equationNuclear chemistryChemical Engineering Journal
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Validation of a high-performance chromatographic method for determination of cefotaxime in biological samples

1999

An analytical method for detecting and quantifying cefotaxime in plasma and several tissues is described. The method was developed and validated using plasma and tissues of rats. The samples were analyzed by reversed phase liquid chromatography (HPLC) with UV detection (254 nm). Calibration graphs showed a linear correlation (r > 0.999) over the concentration ranges of 0.5–200 μg/mL and 1.25–25 μg/g for plasma and tissues, respectively. The recovery of cefotaxime from plasma standards prepared at the concentrations of 25 μg/mL and 100 μg/mL was 98.5 ± 3.5% and 101.8 ± 2.2%, respectively. The recovery of cefotaxime from tissue standards of liver, fat and muscle, prepared at the concentration…

ChromatographyCefotaximePharmacokineticsChemistryCoefficient of variationBlood plasmamedicineReversed-phase chromatographyBiochemistryQuantitative analysis (chemistry)High-performance liquid chromatographyAntibacterial agentmedicine.drugFresenius' Journal of Analytical Chemistry
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Determination of major human cytochrome P450s activities in 96-well plates using liquid chromatography tandem mass spectrometry.

2007

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. Evaluation of the effect of NCEs on human CYP450 enzyme activities is a key issue in pharmaceutical development as it may explain inter-subject variability, drug-drug interactions, non-linear pharmacokinetics and toxic effects. A liquid chromatography tandem mass spectrometry (HPLC-MS/MS) method has been developed for the fast and routine analysis of major human CYP450s enzyme activities (CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4) in primary hepatocyte cell cultures. The high sensitivity and selectivity of mass …

ChromatographyChemistryDrug discoveryCYP1A2Drug Evaluation PreclinicalGeneral MedicineToxicologyTandem mass spectrometryMass spectrometrySubstrate SpecificityPharmacokineticsCytochrome P-450 Enzyme SystemLiquid chromatography–mass spectrometryTandem Mass SpectrometryDrug DesignHepatocytesHumansCYP2A6Drug metabolismCells CulturedChromatography LiquidToxicology in vitro : an international journal published in association with BIBRA
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Nonenzymatic glycation reaction of folate with reducing sugars: A case study on [6S]-5-methyltetrahydrofolate and fructose

2006

In the Maillard reaction, free amino groups react with reducing sugars to form nonenzymatic glycation products. It has recently been shown that in the presence of reducing sugars (i.e. fructose) folic acid is subjected to a non-enzymatic glycation reaction, which may represent an important pathway of folate degradation besides the established oxidative degradation pathways. In the current study, the thermal stability of [6S]-5-methyltetrahydrofolic acid ([6S]-5-CH3H4PteGlu, 0.4µM), the predominant naturally occuring folate derivate, was investigated on a qualitative and kinetic basis in the presence of different fructose concentrations (0-3M) in milliQ water (8.11ppm O2). Samples were isoth…

ChromatographyChemistryFirst-order reactionKineticsFructoseMaillard reactionsymbols.namesakechemistry.chemical_compoundReaction rate constantGlycationsymbolsOrganic chemistryThermal stabilityDestabilisation13th World Congress of Food Science & Technology
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Thermally Induced Isomerisation Kinetics of the 9c11t and 10t12c Conjugated Linoleic Acids in Triacylglycerols as Studied by FT-IR Spectrometry Aided…

2014

Published version of an article from the journal:The Open Spectroscopy Journa. Also available from the publisher:http://dx.doi.org/10.2174/1874383801004010041. Open Access Isomerisation kinetics of the 9c11t and 10t12c Conjugated Linoleic Acids (CLA) in triaclglycerols at isothermal conditions (250, 280 and 325oC) has been studied by infrared spectroscopy. Fifteen micro liter portions of the glycerides were placed in micro glass ampoules and sealed under nitrogen. Several glass tubes containing the same triacylglycerols were then subjected to thermal treatment. The glass tubes were removed at regular time intervals, cut open, and a part of the contents in each glass tube analysed by infrare…

ChromatographyChemistryKineticsOrganic chemistryVDP::Medical disciplines: 700::Basic medical dental and veterinary science disciplines: 710::Medical biochemistry: 726VDP::Mathematics and natural science: 400::Chemistry: 440::Organic chemistry: 441Gas chromatographyConjugated systemFourier transform infrared spectroscopySpectroscopyMass spectrometryIsomerizationThe Open Spectroscopy Journal
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Impact of acidic/hydrothermal treatment on pore structural and chromatographic properties of porous silicas

1991

Abstract A series of commercial silicas and a laboratory made product were subjected to acidic/hydrothermal treatment with solutions of HCI, HNO3, H2SO4 and HF. The concentration of acid and the temperature and duration of treatment were varied. The specific surface area, content of metal impurities, types and concentration of surface hydroxyl and siloxane groups and crystallinity were determined for native and treated silicas. Only changes in the structural order of the surface could be assessed by means of 19Si cross-polarization magic angle spinning NMR spectrometry and electron diffraction. The native and acid-treated silicas were surface modified to n-octyl derivatives and tested under…

ChromatographyChemistryOrganic ChemistryKineticsGeneral MedicineReversed-phase chromatographyBiochemistryAnalytical ChemistryCrystallinitychemistry.chemical_compoundElectron diffractionSiloxaneSpecific surface areaMagic angle spinningPorosityJournal of Chromatography A
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A theoretical plate model accounting for slow kinetics in chromatographic elution.

2011

The chromatographic elution has been studied from different perspectives. However, in spite of the simplicity and evident deficiencies of the plate model proposed by Martin and Synge, it has served as a basis for the characterization of columns up-to-date. This approach envisions the chromatographic column as an arbitrary number of theoretical plates, each of them consisting of identical repeating portions of mobile phase and stationary phase. Solutes partition between both phases, reaching the equilibrium. Mobile phase transference between the theoretical plates is assumed to be infinitesimally stepwise (or continuous), giving rise to the mixing of the solutions in adjacent plates. This yi…

ChromatographyComputer simulationElutionChemistryOrganic ChemistryKineticsGeneral MedicineModels TheoreticalKinetic energyBiochemistryAnalytical ChemistryVolumetric flow rateSolutionsKineticsPharmaceutical PreparationsMass transferPartition (number theory)Theoretical plateChromatography High Pressure LiquidJournal of chromatography. A
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Effects of polysorbate 80 on amiodarone intestinal absorption in the rat

1995

Abstract Amiodarone is a widely used anti-arrhythmic agent which shows physico-chemical properties that are highly suitable for diffusion across lipophilic absorbing membranes, however,.its low aqueous solubility could represent the rate-limiting step for absorption, making it erratic and variable. In a previous paper, the influence of an anionic surfactant (sodium lauryl sulphate) at variable supramicellar concentrations was studied. The absorption rate constants of amiodarone decreased as the surfactant concentration increased, and absorption was unusually fast at lower surfactant concentrations. The previously proposed equations for interpreting the relationships between the amiodarone a…

ChromatographyDiffusionPharmaceutical ScienceAmiodaronePolyvinyl alcoholIntestinal absorptionchemistry.chemical_compoundMembranePharmacokineticschemistryPulmonary surfactantmedicineAbsorption (chemistry)medicine.drugInternational Journal of Pharmaceutics
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Ion-exchange voltammetry at a surfactant-doped electrode: model of mass transfer kinetics to an anionic surface-charged electrode and its application…

2000

cited By 10; International audience; A theoretical model of mass transfer kinetics was developed for investigating the accumulation of cationic compounds at an anionic surfactant-doped screen-printed electrode. It was extended to an enzyme-generated cationic product for the indirect determination of alkaline phosphatase (AP). The model takes into account the analyte depletion, the kinetics of the ion-exchange reaction-diffusion and the kinetics of the enzymatic reaction. The relationship between the ion-exchange voltammetric anodic peak current and the enzyme incubation/accumulation time for a given concentration of AP was established and the validity of the theoretical model was verified e…

ChromatographyIon exchangeGeneral Chemical EngineeringKineticsInorganic chemistryCationic polymerizationSubstrate (chemistry)02 engineering and technologyBuffer solution010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryElectrochemical gas sensorchemistry.chemical_compoundchemistryElectrodeElectrochemistry[CHIM]Chemical Sciences0210 nano-technologyVoltammetry
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