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Determination of tadalafil in small volumes of plasma by high-performance liquid chromatography with UV detection
Tadalafil is a potent reversible phosphodiesterase-5 inhibitor used for the treatment of erectile dysfunction. This study describes a simple and sensitive high-performance liquid chromatographic (HPLC) method for the determination of tadalafil in 50 μl of rat plasma. Tadalafil and the internal stand...
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Published in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2005-08, Vol.822 (1), p.278-284 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Tadalafil is a potent reversible phosphodiesterase-5 inhibitor used for the treatment of erectile dysfunction. This study describes a simple and sensitive high-performance liquid chromatographic (HPLC) method for the determination of tadalafil in 50
μl of rat plasma. Tadalafil and the internal standard lamotrigine were extracted with 0.5
ml of
tert-butyl methyl ether, after the samples alkalinized with 20
μl of sodium hydroxide solution (1N). Chromatographic separation was achieved on a C18 column with the mobile phase of acetonitrile–water containing 20
mM phosphate buffer (pH 7) (35/65, v/v), at a flow rate of 1
ml/min. The eluant was detected at 290
nm. The retention time was about 4.5
min for lamotrigine and 15
min for tadalafil. No endogenous substances were found to interfere. Calibration curves were linear from 10 to 2000
ng/ml. The recovery of tadalafil from plasma was greater than 77%. The limit of quantitation was 10
ng/ml. The intra- and inter-day imprecision (expressed as coefficient of variation, C.V.) did not exceed 10.7%, and the accuracy was within 5.9% deviation of the nominal concentration. The method is suitable in pharmacokinetic investigation and monitoring tadalafil concentration. |
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ISSN: | 1570-0232 1873-376X |
DOI: | 10.1016/j.jchromb.2005.06.017 |