Publications by authors named "Marie Lecoeur-Lorin"

The enantioseparation of fenamiphos and its two main metabolites (fenamiphos sulfoxide and fenamiphos sulfone) were simultaneously achieved by CE by using a dual CD system. A mixture of 25 mM carboxymethyl-beta-CD and 10 mM hydroxypropyl-alpha-CD was added to the acetic acid/ammonia (ionic strength=50 mM, pH 5) buffer and was suitable for the baseline resolution of all stereoisomers of analytes. A further addition of 5% methanol to the BGE increased significantly the resolution between the diastereoisomers of fenamiphos sulfoxide.

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A capacitively coupled contactless conductivity detection (C4D) system for CE with a flexible detection cell was applied for the enantioseparation of small chiral underivatized amines using chiral crown ether or CD as chiral selector. Since these compounds are poorly UV-active, C4D was an alternative detection mode. The composition (ionic strength, pH, chiral selector) of the electrolyte was optimized in order to be suitable for C4D.

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The determination of the enantiomeric excess (e.e.) of a basic drug has been investigated in LC using a nonchiral stationary phase and a circular dichroism (CD) detector in order to avoid expensive chiral columns.

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The need for a rapid and cheap chromatographic technique for the simultaneous determination of diastereoisomeric and chemical purities of a drug has led to develop a non-enantioselective HPLC method on a porous graphitic carbon (PGC) sorbent and by using circular dichroism (CD) detection. Among a lot of non-chiral chromatographic supports tested, PGC was the only one allowing the separation of all benzoxathiepin diastereoisomers. After optimization of the chromatographic conditions, a mobile phase composed of chloroform, acetonitrile and methanol was suitable to elute the diastereoisomers with their related chemical impurities in less than 20 min by gradient mode.

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