Determination of verapamil by adsorptive stripping voltammetry in urine and pharmaceutical formulations
A sensitive reduction peak of verapamil is obtained by adsorptive stripping voltammetry in 0.01 M phosphate (pH 7.4) at an accumulation time of 30 s. The peak potential is −1.81 V (vs. Ag/AgCl). The peak current is directly proportional to the concentration of verapamil (1×10 −8–1×10 −6 M), with a 3...
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Published in | Journal of pharmaceutical and biomedical analysis Vol. 30; no. 4; pp. 921 - 929 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
07.11.2002
Elsevier Science |
Subjects | |
Online Access | Get full text |
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Summary: | A sensitive reduction peak of verapamil is obtained by adsorptive stripping voltammetry in 0.01 M phosphate (pH 7.4) at an accumulation time of 30 s. The peak potential is −1.81 V (vs. Ag/AgCl). The peak current is directly proportional to the concentration of verapamil (1×10
−8–1×10
−6 M), with a 3
σ detection limit of 5×10
−10 M (0.246 ng/ml). The R.S.D. at the 1×10
−7 M level is 1.8%. The interference of some metal ions, and some amino acids, and the application of the method to analysis of urine, and pharmaceutical formulations are described. The method is simple (no extraction), rapid (30 s accumulation time), sensitive (the detection limit of verapamil is 0.491 ng/ml), reproducible(within day R.S.D. of 1.28–1.8%), and suitable for routine analysis of verapamil, urine, and pharmaceutical formulation. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/S0731-7085(02)00322-9 |