6533b7d9fe1ef96bd126d75c
RESEARCH PRODUCT
Hydrophobicity of ionisable compounds studied by countercurrent chromatography
Samuel Carda-brochAlain BerthodAmélie LevetMaría-josé Ruíz-angelsubject
OctanolAdrenergic beta-AntagonistsHydrophobicityAnalytical chemistryIonic bonding01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCountercurrent chromatographyPhase (matter)MoleculeDiureticsCountercurrent DistributionAqueous solutionChromatography010405 organic chemistryHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryOctanol–water partition coefficientsGeneral Medicine0104 chemical sciencesPartition coefficientPharmaceutical PreparationschemistryCountercurrent chromatographyIonisable compoundsHydrophobic and Hydrophilic Interactionsdescription
Countercurrent chromatography (CCC) is a liquid chromatography technique in which the stationary phase is also a liquid. The main chemical process involved in solute separation is partitioning between the two immiscible liquid phases: the mobile phase and the support-free liquid stationary phase. The octanol-water partition coefficients (P(o/w)) is the accepted parameter measuring the hydrophobicity of molecules. It is considered to estimate active principle partitioning over a biomembrane. It was related to the substance biological activity. CCC is able to work with an octanol stationary phase and an aqueous mobile phase. In this configuration, CCC is a useful and easy alternative to measure directly the P(o/w) of the molecules compared to other methods including the classical and tedious shake-flask method. Three ketones are used as model compounds to illustrate the CCC protocol of P(o/w) measurement. The focus of this work is put on ionisable molecules whose apparent P(o/w) is completely changed by ionization. β-Blockers, diuretics and sulfonamides are compound classes that were studied. Some of the experimentally determined P(o/w) coefficients of the molecular forms disagreed with calculated and experimental values available in the literature. The P(o/w) coefficients of the ionic forms and the acidity constants were also calculated using a theoretical model. Relationships between biological properties and hydrophobicity are also discussed.
year | journal | country | edition | language |
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2011-09-01 | Journal of Chromatography A |