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Development and validation of a bioanalytical method for the quantification of diltiazem and desacetyldiltiazem in plasma by capillary zone electrophoresis.

作者信息

Coors C, Schulz H G, Stache F

机构信息

3M Medica, Analytical Development, Borken, Germany.

出版信息

J Chromatogr A. 1995 Nov 24;717(1-2):235-43. doi: 10.1016/0021-9673(95)00622-4.

DOI:10.1016/0021-9673(95)00622-4
PMID:8520677
Abstract

A CZE method for the quantification of diltiazem and desacetyldiltiazem in plasma was developed and validated. Separation was accomplished at pH 2.5 in a 0.044 M phosphate buffer. Sample preparation was performed by liquid-liquid extraction and no interferences with plasma compounds were detected. The calibration graph is linear over the range 5-250 ng/ml with verapamil as internal standard. The precision and accuracy are better than 13% at 5 ng/ml, and better than 10% between 10 and 250 ng/ml. The long-term reliability of the CZE system was checked over a 3-month period. The CZE method is a useful alternative to the already established HPLC method.

摘要

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