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Fast enantiomeric separation of basis drugs by electrokinetic chromatography. Application to the quantitation of terbutaline in a pharmaceutical preparation
Author(s) -
GarcíaRuiz Carmen,
Marina Maria Luisa
Publication year - 2001
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200109)22:15<3191::aid-elps3191>3.0.co;2-g
Subject(s) - chemistry , enantiomer , chromatography , terbutaline , electrokinetic phenomena , micellar electrokinetic chromatography , clenbuterol , sodium dodecyl sulfate , ammonium acetate , cyclodextrin , salbutamol , detection limit , high performance liquid chromatography , organic chemistry , medicine , asthma
Electrokinetic chromatography (EKC) using micelles of bile salts alone or mixed with sodium dodecyl sulfate (SDS) and neutral, anionic, or cationic cyclodextrins (CDs) in the separation buffer has been employed in order to achieve fast enantiomeric separation of basic drugs. A study of the enantiomeric separation ability of these chiral selectors concerning four basic drugs (epinephrine, terbutaline, clenbuterol, and salbutamol) has been carried out under different experimental conditions. The best chiral selectors to perform the enantiomeric separation of these drugs were neutral β‐CD derivatives, specifically permethylated β‐CD PM‐β‐CD. The effect of the PM‐β‐CD concentration, temperature, and applied voltage on the enantiomeric resolution of the basic drugs was investigated. The use of a 25 m M ammonium acetate buffer (pH 5.0), 30 m M in PM‐ß‐CD together with an applied voltage of 20 kV and a temperature of 15°C enabled the individual and fast enantiomeric separation of epinephrine, norepinephrine, terbutaline, clenbuterol, and salbutamol each one into its two enantiomers in less than 3 min. The EKC method was validated (precision and accuracy) to quantitate terbutaline in a pharmaceutical preparation, obtaining a limit of detection of 4 νg/mL.