חיפוש מתקדם
Journal of Liquid Chromatography
Teitelbaum, Z., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
Ben-Dom, N., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
Terry, S., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
A reliable, highly reproducible, accurate and time-efficient high performance liquid chromatographic (HPLC) method to measure atenolol concentration in human plasma was developed and validated. Sample clean-up consists of simple and efficient liquid-liquid extraction (mean recovery 103%) which allows a high sample throughput. Chromatography on a CN-propyl column yields symmetrical and well resolved peaks for atenolol and for the internal standard (metoprolol) without any interference from endogenous plasma components. Using 1 ml plasma samples the method has a limit of detection of 12.6 ng/ml (calculated at a 99.9% confidence level) with %CV (precision) s 8.8% and bias (accuracy) s 3.8% for concentrations in the range of 10 - 1000 ng/ml. We now routinely use this method in human pharmacokinetic studies of atenolol dosage forms. Copyright © 1991 by Marcel Dekker, Inc.
פותח על ידי קלירמאש פתרונות בע"מ -
הספר "אוצר וולקני"
אודות
תנאי שימוש
A liquid chromatographic method for the determination of atenolol in human plasma
14
Teitelbaum, Z., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
Ben-Dom, N., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
Terry, S., Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona, 70450, Israel
A liquid chromatographic method for the determination of atenolol in human plasma
A reliable, highly reproducible, accurate and time-efficient high performance liquid chromatographic (HPLC) method to measure atenolol concentration in human plasma was developed and validated. Sample clean-up consists of simple and efficient liquid-liquid extraction (mean recovery 103%) which allows a high sample throughput. Chromatography on a CN-propyl column yields symmetrical and well resolved peaks for atenolol and for the internal standard (metoprolol) without any interference from endogenous plasma components. Using 1 ml plasma samples the method has a limit of detection of 12.6 ng/ml (calculated at a 99.9% confidence level) with %CV (precision) s 8.8% and bias (accuracy) s 3.8% for concentrations in the range of 10 - 1000 ng/ml. We now routinely use this method in human pharmacokinetic studies of atenolol dosage forms. Copyright © 1991 by Marcel Dekker, Inc.
Scientific Publication
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