Search results for "HILIC"

showing 10 items of 745 documents

CEC column behaviour of butyl and lauryl methacrylate monoliths prepared in non-aqueous media

2009

Polymeric monolithic stationary phases for capillary electrochromatography were prepared using two bulk monomers, butyl methacrylate (BMA) and lauryl methacrylate (LMA), by in situ polymerization in non-aqueous media. The effect of 1,4-butanediol/1-propanol ratio on porous properties was investigated separately for each monomer, keeping the proportion of monomers to pore-forming solvents fixed at 40:60 wt:wt. Also, mixtures of BMA and LMA at different 1,4-butanediol/1-propanol ratios were studied for tailoring the morphological features of the monolithic columns. The chromatographic performance of the different columns was evaluated by means of van Deemter plots of polycyclic aromatic hydro…

Van Deemter equationMaterials scienceNitrogenClinical Biochemistry1-PropanolMethacrylateBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary ElectrochromatographyPolycyclic Aromatic HydrocarbonsIn situ polymerizationButylene GlycolsPorosityCapillary electrochromatographyChromatographyMercuryPorosimetryMonomerchemistryChemical engineeringMicroscopy Electron ScanningSolventsMethacrylatesAdsorptionHydrophobic and Hydrophilic InteractionsPorosityLauryl methacrylateELECTROPHORESIS
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Retention pharmacokinetic and pharmacodynamic parameter relationships of antihistamine drugs using biopartitioning micellar chromatography

2001

Abstract Antihistamines are drugs which act by competitive inhibition of the H1 or H2 histamine receptors. Little has been known about their clinical pharmacokinetics and biological responses until the last few years. In this paper, we propose quantitative retention–activity relationship, QRAR, models based on the retention data of antihistamines in a biopartitioning micellar chromatography (BMC) system using a Brij35 mobile phase for describing pharmacokinetic parameters such as half-life and volume of distribution, or the pharmacodynamic parameters, therapeutic plasma levels, lethal doses and drug-receptor dissociation constant. The predictive ability of these models is statistically vali…

Volume of distributionQuantitative structure–activity relationshipChromatographyChemistrymedicine.medical_treatmentQuantitative Structure-Activity RelationshipGeneral ChemistryHigh-performance liquid chromatographyDissociation constantPharmacokineticsPharmacodynamicsLipophilicityHistamine H1 AntagonistsmedicineSpectrophotometry UltravioletAntihistamineChromatography LiquidJournal of Chromatography B: Biomedical Sciences and Applications
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Effect of Ligands on HP-Induced Unfolding and Oligomerization of β-Lactoglobulin

2020

ABSTRACTTo probe intermediate states during unfolding and oligomerization of proteins remains a major challenge. High pressure (HP) is a powerful tool for studying these problems, revealing subtle structural changes in proteins not accessible by other means of denaturation. Bovine β-lactoglobulin (BLG), the main whey protein, has a strong propensity to bind various bioactive molecules, such as retinol and resveratrol, two ligands with different affinity and binding sites. By combining in situ HP-small-angle neutron scattering (SANS) and HP-UV/visible absorption spectroscopy, we report the specific effects of these ligands on 3D conformational and local changes in BLG induced by HP. Dependin…

Whey proteinProtein Folding[SDV]Life Sciences [q-bio]BiophysicsAb initioLactoglobulins010402 general chemistryLigands01 natural sciences03 medical and health sciences0404 agricultural biotechnologyAnimalsDenaturation (biochemistry)[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyBinding site030304 developmental biology0303 health sciencesBinding SitesChemistry04 agricultural and veterinary sciencesArticlesLigand (biochemistry)040401 food science0104 chemical sciencesCovalent bondBiophysicsUnfolded protein responseProtein foldingCattleHydrophobic and Hydrophilic Interactions
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Integrating analytical resolutions in non-targeted wine metabolomics

2015

Direct injection Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS), and ultra-high performance liquid chromatography coupled to mass spectrometry (UPLC/MS) were combined for the non-targeted analysis of wine metabolites. The unrivalled resolution on mass measurement allowed by the former and the separation ability of isomeric and isobaric substances by the latter, clearly increases the scope of detectable unknown metabolites in wines. Such methodology is illustrated through the comparison of chemical spaces of a young and an older Pinot noir wine. RP and HILIC chromatography could reveal up to five isomers for a given mass, throughout the explored mass range. CHO, CHOS …

WineChromatographyResolution (mass spectrometry)ChemistryHydrophilic interaction chromatographydigestive oral and skin physiologyOrganic Chemistryfood and beveragesMass spectrometryBiochemistryHigh-performance liquid chromatographyFourier transform ion cyclotron resonanceMetabolomicsDrug DiscoveryWine chemistryTetrahedron
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Surface properties of Saccharomyces cerevisiae lees during sparkling wine ageing and their effect on flocculation

2009

Cell surface properties were determined for the first time for lees of Saccharomyces cerevisiae, and they proved to be significantly dependent on the time of sparkling wine ageing on lees. Cell surface hydrophobicity decreased from approximately 44% to 11% of affinity to hexadecane. Electron acceptor capacity (calculated as % affinity to ethyl acetate-% affinity to decane) increased from approximately -27% to 10 % and zeta potential from approximately -4 to 6mV. Mannoproteins are released from the external cell wall layer during the autolytic process, as confirmed by TOF-SIMS analysis of the cell wall chemical composition. This could explain the modifications of lees cell surface properties…

WineFlocculationChromatographySurface PropertiesFlocculationWineSaccharomyces cerevisiaeGeneral MedicineDecaneHexadecaneMicrobiologyLeeschemistry.chemical_compoundchemistryAgeingFermentationZeta potentialHydrophobic and Hydrophilic InteractionsFood ScienceWinemakingInternational Journal of Food Microbiology
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Extension of the linear solvent strength retention model including a parameter that describes the elution strength changes in liquid chromatography.

2020

Modelling the retention behaviour of solutes in liquid chromatography, based on the composition of the mobile phase is a common task in the chromatographic practice. Along the development of liquid chromatography (LC), several models have been proposed to help in understanding the retention mechanisms, and especially, allow the prediction of retention times with optimisation purposes. Particular models are used for different LC modes, such as normal phase (NPLC), reversed phase (RPLC), hydrophilic interaction (HILIC), and micellar (MLC). In this work, a general equation is proposed that includes a parameter (the elution degree, g), which characterises the way the elution strength varies wit…

Work (thermodynamics)ChromatographyElutionChemistryHydrophilic interaction chromatographyNormal phase010401 analytical chemistryOrganic ChemistryGeneral Medicine010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistrySolvent strengthModels ChemicalGeneral equationPhase (matter)SolventsGradient elutionHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of chromatography. A
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Explicit Solvation Matters: Performance of QM/MM Solvation Models in Nucleophilic Addition

2018

Nucleophilic addition onto a carbonyl moiety is strongly affected by solvent, and correctly simulating this solvent effect is often beyond the capability of single-scale quantum mechanical (QM) models. This work explores multiscale approaches for the description of the reversible and highly solvent-sensitive nucleophilic N|···C=O bond formation in an Me2N–(CH2)3–CH=O molecule. In the first stage of this work, we rigorously compare and test four recent quantum mechanical/molecular mechanical (QM/MM) explicit solvation models, employing a QM description of water molecules in spherical regions around both the oxygen and the nitrogen atom of the solute. The accuracy of the models is benchmarked…

Work (thermodynamics)Nucleophilic additionMaterials science010304 chemical physicsSolvationThermodynamics010402 general chemistry01 natural sciencesArticle0104 chemical sciencesComputer Science ApplicationsQM/MMNucleophile0103 physical sciencesMoleculePhysical and Theoretical ChemistrySolvent effectsQuantumJournal of Chemical Theory and Computation
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Testing experimental designs in liquid chromatography (I): Development and validation of a method for the comprehensive inspection of experimental de…

2020

The basis of interpretive optimisation in liquid chromatography is the prediction of resolution, from appropriate solute retention models. The reliability of the process depends critically on the quality of the experimental design. This work develops, validates and applies a general methodology aimed to evaluate the quality of any training experimental design, which will be applied in Part II to design optimisation. The methodology is based on the systematic evaluation of the uncertainties associated to the prediction of retention times in comprehensive scans of both isocratic and gradient experimental conditions. It is able to evaluate comprehensively experimental designs of arbitrary comp…

Work (thermodynamics)SulfonamidesChromatographyBasis (linear algebra)ChemistryDesign of experiments010401 analytical chemistryOrganic ChemistryProcess (computing)General Medicine010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistrySet (abstract data type)NK modelResearch DesignSolventsLack-of-fit sum of squaresHydrophobic and Hydrophilic InteractionsReliability (statistics)Chromatography LiquidJournal of chromatography. A
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Synthesis of new asymmetric xanthene dyes via catalyst-free SNAr with sulfur nucleophiles

2014

Addition of a single functional handle to the tricyclic moiety of fluorescein results in asymmetric xanthene dyes. Our synthesis of a new class of asymmetric xanthenes proceeds via an unusual SNAr with sulfur nucleophiles on electron rich aromatic xanthenes scaffolds in the absence of a metal catalyst. The resulting 3'-thioethers exhibit high photostability and are conveniently converted into reactive dyes for macromolecule labelling.

XantheneAzidesOrganic Chemistrychemistry.chemical_elementElectronsHydrogen-Ion ConcentrationSulfidesPhotochemistryBiochemistrySulfurCombinatorial chemistryCatalysisCatalysischemistry.chemical_compoundSpectrometry FluorescenceXantheneschemistryNucleophileNucleophilic aromatic substitutionMoietyPhysical and Theoretical ChemistrySulfurFluorescent DyesMacromoleculeOrganic & Biomolecular Chemistry
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ChemInform Abstract: Synthesis of New Asymmetric Xanthene Dyes via Catalyst-Free SNAr with Sulfur Nucleophiles.

2014

Addition of a single functional handle to the tricyclic moiety of fluorescein results in asymmetric xanthene dyes. Our synthesis of a new class of asymmetric xanthenes proceeds via an unusual SNAr with sulfur nucleophiles on electron rich aromatic xanthenes scaffolds in the absence of a metal catalyst. The resulting 3′-thioethers exhibit high photostability and are conveniently converted into reactive dyes for macromolecule labelling.

Xanthenechemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionLabellingMoietychemistry.chemical_elementGeneral MedicineCombinatorial chemistrySulfurCatalysisMacromoleculeChemInform
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