Direct determination of celiprolol in human urine using on-line coupled ITP-CZE method with fiber-based DAD

• Published in: Electrophoresis 2008-11, Vol.29 (22), p.4561-4567
• Main Authors: Mikus, Peter, Maráková, Katarína, Marák, Jozef, Planková, Alexandra, Valásková, Iva, Havránek, Emil
• Format: Article
• Language: English
• Subjects: Adrenergic beta-Antagonists - urine; Buffers; Celiprolol; Celiprolol - urine; Column-coupling electrophoresis; CZE; DAD; Electrophoresis - methods; Electrophoresis, Capillary - methods; Female; Humans; Hydrogen-Ion Concentration; ITP; Reproducibility of Results; Sensitivity and Specificity
• ISSN: 0173-0835; 1522-2683
• DOI: 10.1002/elps.200800079

The present work illustrated possibilities of column-coupling electrophoresis combined with DAD for the direct quantitative determination of trace drug (celiprolol, CEL) in clinical human urine samples. ITP, on-line coupled with CZE, served as an ideal injection technique (high sample load capacity, narrow and sharp drug zone). Moreover, the ITP provided an effective on-line sample pretreatment (preseparation, purification and preconcentration of the drug) producing analyte zone suitable for its direct detection and quantitation in CZE stage. Spectral DAD in comparison with single wavelength ultraviolet detection enhanced value of analytical information (i) verifying purity (i.e., spectral homogeneity) of drug zone (according to differences in spectrum profiles when compared tested and reference drug spectra) and (ii) indicating zones/peaks with spectra similar to the drug spectrum (potential structurally related metabolites). The characterization of trace analyte signals superposed on the baseline noise was more definite thanks to the application of background correction and smoothing procedure to the raw DAD spectra (producing relevant spectral response). The proposed ITP-CZE-DAD method was characterized by favorable performance parameters for CEL in urine matrices {e.g., the lower limit of quantification was 9.7 ng/mL, RSD and relative error of the determinations were lower than 3% (precision) and 1% (accuracy), respectively, analyte peak exhibited spectral homogeneity (reflecting separation selectivity), separation efficiency was 84 500 theoretical plates} and successfully applied in a trial pharmacokinetic study of CEL.