TY - JOUR
T1 - Simultaneous assay of felbamate plus carbamazepine, phenytoin, and their metabolites by liquid chromatography with mobile phase optimization
AU - Remmel, Rory P.
AU - Miller, Scott A.
AU - Graves, Nina M.
PY - 1990/1
Y1 - 1990/1
N2 - Felbamate is an investigational antiepileptic drug (AED) in clinical trials. A high-performance liquid chromatographic method for the simultaneous analysis of felbamate, phenytoin (PHT), 5-(p-hydroxyphenyl)-5-phenylhydantoin, carbamazepine (CBZ), carbamazepine-10,11-epoxide, and carbamazepine-10,11-diol in serum was developed by a mobile phase optimization technique. Capacity factors for the compounds of interest and 12 other AEDs and metabolites were determined with mixtures of methanol, acetonitrile, or tetrahydrofuran and a 0.01 M ammonium phosphate buffer, pH 6.5, on a reversed-phase C8 column. An optimized mobile phase composition was determined that could separate the compounds of interest and three internal standards in <15 min. Serum was extracted with CH2Cl2/ethyl acetate (2:1) after addition of three internal standards. The method was validated for within-day and between-day precision and accuracy for the six compounds. Coefficients of variation were generally <10% at all concentrations and <5% in the typical therapeutic range for each compound. The lower limit of detection was estimated at 0.2 µg/ml for CBZ and its metabolites and 0.5 µg/ml for felbamate and PHT. For felbamate, the lowest point on the standard curve was 1.88 µg/ml with a between-day variability of 10.3%. The assay was used to determine the serum concentrations of PHT and CBZ and its metabolites in a subject before, during, and after felbamate therapy.
AB - Felbamate is an investigational antiepileptic drug (AED) in clinical trials. A high-performance liquid chromatographic method for the simultaneous analysis of felbamate, phenytoin (PHT), 5-(p-hydroxyphenyl)-5-phenylhydantoin, carbamazepine (CBZ), carbamazepine-10,11-epoxide, and carbamazepine-10,11-diol in serum was developed by a mobile phase optimization technique. Capacity factors for the compounds of interest and 12 other AEDs and metabolites were determined with mixtures of methanol, acetonitrile, or tetrahydrofuran and a 0.01 M ammonium phosphate buffer, pH 6.5, on a reversed-phase C8 column. An optimized mobile phase composition was determined that could separate the compounds of interest and three internal standards in <15 min. Serum was extracted with CH2Cl2/ethyl acetate (2:1) after addition of three internal standards. The method was validated for within-day and between-day precision and accuracy for the six compounds. Coefficients of variation were generally <10% at all concentrations and <5% in the typical therapeutic range for each compound. The lower limit of detection was estimated at 0.2 µg/ml for CBZ and its metabolites and 0.5 µg/ml for felbamate and PHT. For felbamate, the lowest point on the standard curve was 1.88 µg/ml with a between-day variability of 10.3%. The assay was used to determine the serum concentrations of PHT and CBZ and its metabolites in a subject before, during, and after felbamate therapy.
KW - Analysis
KW - Carbamazepine
KW - Felbamate
KW - High-performance liquid chromatography
KW - Optimization
KW - Phenytoin
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U2 - 10.1097/00007691-199001000-00017
DO - 10.1097/00007691-199001000-00017
M3 - Article
C2 - 2305427
AN - SCOPUS:0025174657
SN - 0163-4356
VL - 12
SP - 90
EP - 96
JO - Therapeutic Drug Monitoring
JF - Therapeutic Drug Monitoring
IS - 1
ER -