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Capillary electrochromatographic analysis of barbiturates in serum

A capillary electrochromatographic method was developed for the separation of barbiturates. The separation was optimized in a 75 μm ID capillary, packed with 3‐(1,8‐naphthalimido)propyl‐modified silyl silica gel (NAIP), studying the effect of buffer pH, buffer concentration, and mobile phase composi...

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Bibliographic Details
Published in:Electrophoresis 2004-02, Vol.25 (4-5), p.594-599
Main Authors: Ohyama, Kaname, Wada, Mitsuhiro, Lord, Gwyn A., Ohba, Yoshihito, Fujishita, Osamu, Nakashima, Kenichiro, Lim, Chang Kee, Kuroda, Naotaka
Format: Article
Language:English
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Summary:A capillary electrochromatographic method was developed for the separation of barbiturates. The separation was optimized in a 75 μm ID capillary, packed with 3‐(1,8‐naphthalimido)propyl‐modified silyl silica gel (NAIP), studying the effect of buffer pH, buffer concentration, and mobile phase composition. Using an applied voltage of 20 kV and the short‐end injection method (9 cm capillary effective length), the mobile phase of 1.0 mM citrate buffer (pH 5.0) containing 40% methanol provided the baseline separation of barbital, phenobarbital, secobarbital, and thiopental (internal standard) in less than 4.5 min. The method was successfully applied to the analysis of barbiturates in human serum. Under the optimal conditions, good repeatability and linearity were obtained in the range of 2.90–43.29 μg/mL for barbital, phenobarbital, and secobarbital.
ISSN:0173-0835
1522-2683
DOI:10.1002/elps.200305703