Search results for "Partition coefficient"

showing 10 items of 146 documents

The solubilization site of 5,10,15,20-tetrakis-(2,6-dichlorophenyl)-porphyrin-Mn(III) in DPPC vesicles: A spectrophotometric and tensiometric study

2006

Abstract The solubilization site of 5,10,15,20-tetrakis-(2,6-dichlorophenyl)-porphyrin-Mn(III) (MnTDPPC) in l -α-dipalmitoylphosphatidyl choline (DPPC) vesicles was determined in a systematic UV–vis spectrophotometric study. Measurements of the MnTDPPC absorbance have been conducted at constant temperatures (in the interval 30 °C ≤ T ≤ 48 °C) and varying concentrations of phospholipid. In the entire temperature range, the absorption due to MnTDCCP was found to increase with increasing DPPC concentration, until it reaches a plateau value. The data have been analyzed using a pseudo-phase model yielding the binding constant of MnTDCPP to vesicular aggregates. No significant temperature depende…

ChromatographyChemistryVesicletechnology industry and agricultureAqueous two-phase systemAnalytical chemistryPorphyrinBinding constantHydrophobic effectPartition coefficientAbsorbancechemistry.chemical_compoundColloid and Surface ChemistryAbsorption (chemistry)Colloids and Surfaces A: Physicochemical and Engineering Aspects
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Micellar liquid chromatography: suitable technique for screening analysis.

2002

The screening capability of micellar liquid chromatography (MLC) is discussed using the reported chromatographic data of several sets of compounds (amino acids, beta-blockers, diuretics, phenethylamines, phenols, polynuclear aromatic hydrocarbons, steroids and sulfonamides) and new results (sulfonamides and steroids). The chromatographic data are treated with an interpretive optimisation resolution procedure to obtain the best separation conditions. Usually, the pH and the concentration of surfactant (sodium dodecyl sulfate, SDS, or cetyltrimethylammonium bromide) for the optimal mobile phase were 2.5-3 and0.12 M, respectively. The nature and concentration of organic solvent depended on the…

ChromatographyElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolPartition coefficientchemistry.chemical_compoundColumn chromatographychemistryPharmaceutical PreparationsMicellar liquid chromatographySodium dodecyl sulfateChromatography LiquidJournal of chromatography. A
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Fractal Dimension of Transdermal-Delivery Drug Models: 4-Alkylanilines

2008

Abstract The pathways that exist in porous membranes used to deliver drugs form fractal percolating paths. For a homologous series of 4-alkylanilines, the fractal dimension D is calculated as a model for transdermal-delivery drugs. Program TOPO is used for the calculation of the solvent-accessible surface AS, which is denoted by the centre of a probe, which is allowed to roll on the outside while maintaining contact with the bare molecular surface S. AS depends on the probe radius R. For 4-alkylanilines, the quadrupole moment Θ is doubled. The hydrophobic contribution to AS is doubled while its hydrophilic part remains constant. D increases 11%. Geometric descriptor and topological index re…

ChromatographyMolar concentrationChemistryStereochemistryClinical BiochemistryPharmaceutical ScienceThermodynamicsRadiusBiochemistryFractal dimensionAnalytical ChemistryPartition coefficientHomologous serieschemistry.chemical_compoundFractalTopological indexAbsorption (chemistry)Journal of Liquid Chromatography & Related Technologies
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Universal model for the calculation of all organic solvent–water partition coefficients

1998

Abstract We present the basis for building a universal organic solvation model to calculate solubility in any organic solvent and in water, as well as the organic solvent–water partition coefficient ( P ). Log P values are of the same order of magnitude as reference calculations but for a few cases which are discussed. Normalized log P contributions are sensitive to the rest of the atoms. When comparing porphin with phthalocyanine, the latter results in an amphipathic molecule. For C 70 , the contribution of a–e carbons to log P correlates with the distances from the nearest pentagon. The method has been also applied to benzobisthiazole oligomers and phenyl alcohols.

ChromatographyOrganic ChemistrySolvationThermodynamicsGeneral MedicineBiochemistryAnalytical ChemistryGibbs free energyPartition coefficientsymbols.namesakechemistry.chemical_compoundchemistrysymbolsPhthalocyanineMoleculeOrganic chemistrySolubilityOrder of magnitudePorphinJournal of Chromatography A
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Quantitation of hydrophobicity in micellar liquid chromatography

1999

Abstract Micellar liquid chromatography (MLC) is shown to be a promising technique for measuring the hydrophobicity of solutes. The presence of micelles has a profound effect on the chromatographic characteristics of reversed-phase columns. The linear relationships between the logarithm, log k , of the retention factor and such diverse properties as the number of carbon atoms in homologous series, octanol–water partition coefficients and solvatochromic parameters, which are observed in conventional reversed-phase liquid chromatography (RPLC), are not usually valid in MLC. For series of compounds exhibiting a wide range of hydrophobicity, k itself is linearly related to these properties. The…

ChromatographySolvatochromismAnalytical chemistryReversed-phase chromatographyMicelleMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectHomologous serieschemistry.chemical_compoundchemistryMicellar liquid chromatographySpectroscopyTrAC Trends in Analytical Chemistry
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Effect of the temperature on the release of aroma compounds and on the rheological behaviour of model dairy custard

2008

The influence of temperature was pointed out on the release of aroma compounds from a model dairy dessert and on its rheological behaviour. The recipe chosen for inter-laboratory studies within the programme of COST Action 921 was tested. The custards were flavoured with three aroma compounds belonging to strawberry note. The partition coefficients of three compounds (ethyl butyrate, ethyl hexanoate, cis-3-hexenol) were determined at three temperatures (12 °C: tasting temperature of refrigerated dairy products, 20 °C: room temperature, and 37 °C: mouth temperature). Two textures of the custards were obtained using kappa- and iota-carrageenan. Penetrometry tests characterized the rheological…

ChromatographybiologyEthyl hexanoateGeneral Medicinebiology.organism_classificationAnalytical ChemistryPartition coefficientchemistry.chemical_compoundchemistryRheologyEthyl butyrateCost actionFood scienceAromaFood ScienceFood Chemistry
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Permeability and toxicological profile estimation of organochlorine compounds by biopartitioning micellar chromatography

2008

This paper points out the usefulness of biopartitioning micellar chromatography (BMC) as a high-throughput primary screening tool providing key information about the oral absorption, skin permeability (Kp), brain–blood distribution coefficient (BB) and ecotoxicological parameters such as median lethal concentration (LC50) and bioconcentration factors of 15 organochloride compounds. The retention data of compounds in BMC conditions were interpolated in previously developed quantitative–retention activity relationships by our research group. Results show that the compounds studied readily cross the intestinal barrier (oral absorption >ercnt;) and the blood–brain barrier (log BB >p;0.4). In ad…

Clinical BiochemistryBioconcentrationAbsorption (skin)Models BiologicalBiochemistryPermeabilityAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHydrocarbons ChlorinatedAnimalsHumansDicofolPesticidesMolecular BiologySkinPharmacologyChromatographyChromatographyGeneral MedicineHexachlorobenzeneOrganochlorideBioavailabilityPartition coefficientchemistryBlood-Brain BarrierChlorobenzeneEnvironmental chemistrySoftwareBiomedical Chromatography
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Ethyl Hexanoate Transfer Modeling in Carrageenan Matrices for Determination of Diffusion and Partition Properties.

2007

 ; Aroma compound properties in food matrices, such as volatility and diffusivity, have to be determined to understand the effect of composition and structure on aroma release and perception. This work illustrates the use of mass transfer modeling to identify diffusion and partition properties of ethyl hexanoate in water and in carrageenan matrices with various degrees of structure. The comparison of results obtained with a diffusive model to those obtained with a convective model highlights the importance of considering the appropriate transfer mechanism. Modeling of the preliminary experimental steps ensures correct estimation of the conditions for the main aroma release step. The obtaine…

ConvectionChemical PhenomenaAnalytical chemistryThermodynamicsCarrageenanThermal diffusivity01 natural sciencesPhase TransitionVOLATILE COMPOUNDDiffusionchemistry.chemical_compound0404 agricultural biotechnologyMODELINGAROMA RELEASE[SDV.IDA]Life Sciences [q-bio]/Food engineeringPartition (number theory)Aroma compoundPARTITION COEFFICIENTCaproatesAromabiologyChemistry Physical010401 analytical chemistry[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringEthyl hexanoate04 agricultural and veterinary sciencesGeneral ChemistryMASS TRANSFERbiology.organism_classificationDIFFUSION COEFFICIENT040401 food science0104 chemical sciencesCarrageenanKineticschemistryCONVECTIONOdorantsThermodynamicsVolatilizationGeneral Agricultural and Biological SciencesVolatility (chemistry)
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Potential of biopartitioning micellar chromatography as an in vitro technique for predicting drug penetration across the blood–brain barrier

2004

The blood-brain barrier (BBB) is considered to be the main barrier to drug transport into the central nervous system (CNS). The BBB restricts the passive diffusion of many drugs from blood to brain. The ease with which any particular drug diffuses across the BBB is determined largely by the molecular features of drugs, and it is therefore possible to predict the BBB permeability of a drug from its molecular structure. Biopartitioning micellar chromatography (BMC), a mode of micellar liquid chromatography that uses micellar mobile phases of Brij35 in adequate experimental conditions, can be useful in mimicking the drug partitioning process into biological systems. Retention in BMC depends on…

DrugChromatographyChemistrymedia_common.quotation_subjectClinical BiochemistryCell BiologyGeneral MedicinePenetration (firestop)In Vitro TechniquesModels TheoreticalBlood–brain barrierDrug penetrationBiochemistryIn vitroAnalytical ChemistryPartition coefficientmedicine.anatomical_structureBlood-Brain BarrierMicellar liquid chromatographymedicineRegression AnalysisChromatography Liquidmedia_commonDrug transportJournal of Chromatography B
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Fluoride Complexation of Element 104, Rutherfordium

2004

Fluoride complexation of element 104, rutherfordium (Rf), produced in the 248Cm(18O,5n)261Rf reaction has been studied by anion-exchange chromatography on an atom-at-a-time scale. The anion-exchange chromatographic behavior of Rf was investigated in 1.9-13.9 M hydrofluoric acid together with those of the group-4 elements Zr and Hf produced in the 18O-induced reactions on Ge and Gd targets, respectively. It was found that the adsorption behavior of Rf on anion-exchange resin is quite different from those of Zr and Hf, suggesting the influence of relativistic effects on the fluoride complexation of Rf.

DubniumIon chromatographyInorganic chemistryAnalytical chemistrychemistry.chemical_elementGeneral ChemistryBiochemistryCatalysisPartition coefficientchemistry.chemical_compoundColloid and Surface ChemistryAdsorptionHydrofluoric acidchemistryRutherfordiumFluorideJournal of the American Chemical Society
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