0000000000594133

AUTHOR

M. Catalá-icardo

showing 2 related works from this author

Determination of Amino Acids by Micellar High-Performance Liquid Chromatography and Pre-column Derivatization withO-Phthalaldehyde and N-Acetyl-L-cys…

1995

Abstract Micellar liquid chromatography of proteic primary amino acids with pre-column derivatization with o-phthalaldehyde (OPA) and N-acetyl-L-cysteine was studied, using mobile phases containing a short-chain alcohol. The modification of pH gave a large variation of the retention as a result of the protonation of the carboxylate group of amino acids. Maximum resolution and adequate retentions were achieved with a 0.05 M sodium dodecyl sulphate/3% propanol mobile phase at pH 3. The reproducibility was lower than 1.0% at a 1 × 10−4 M concentration level and between 0.6 and 2.2% for 1 × 10−6 M. The determination of glycine, lysine, methionine and threonine in pharmaceutical formulations gav…

chemistry.chemical_classificationPropanolO-Phthalaldehydechemistry.chemical_compoundChromatographychemistryMicellar liquid chromatographyMolecular MedicineProtonationCarboxylateDerivatizationHigh-performance liquid chromatographyAmino acidJournal of Liquid Chromatography
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Correlation between hydrophobicity of amino acids and retention data in reversed-phase liquid chromatography with micellar eluents

1995

Hydrophobic character is usually expressed in terms of the partition coefficient in 1-octanol-water (log PO/W). However, measurement of this coefficient is often problematic. Retention in micellar liquid chromatography is mainly due to hydrophobic interactions and can also be used as an index of hydrophobicity. A hydrophobicity scale was established with retention data foro-phthalaldehyde (OPA)-N-acetyl-L-cysteine (NAC) amino acid derivatives, using the glycine derivative as reference. Since the OPA-NAC derivatives only differ in the nature of R1 in the amino acid (R1CH(COOH)NH2), in the absence of electrostatic interactions the hydrophobic character of the substituent was responsible for r…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryClinical BiochemistrySubstituentReversed-phase chromatographyBiochemistryAnalytical ChemistryAmino acidPartition coefficientHydrophobic effectchemistry.chemical_compoundMicellar liquid chromatographyGlycineHydrophobicity scalesChromatographia
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