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Clinical Chemistry, Vol 23, 2283-2287, Copyright © 1977 by American Association for Clinical Chemistry
GW Mihaly, JA Phillips, WJ Louis and FJ Vajda
We describe a modified high-performance liquid-chromatographic method for the simultaneous analysis of carbamazepine andits biologically active metabolite, carbamazepine-10, 11-epoxide. Concentrations of both these compounds in the plasma of 35 epileptic patients receiving chronic carbamazepine therapy are presented. Concentrations of carbamazepine in plasma were related to those of carbamazepine-10, 11- epoxide (r - 0.495, P less than 0.05). Total daily doses of carbamazepine were better correlated with plasma concentrations of carbamazepine-10, 11-epoxide (r = 0.714, P less than 0.001) than of carbamazepine (r = 0.269, P greater than 0.05). Close correlations were found between results of the three assay procedures we used to measure plasma carbamazepine concentrations: high-performance liquid chromatography, gas-liquid chromatography, and enzyme immunoassay. Correlation coefficients exceeded 0.97 and regression slopes were near unity, indicating that all three procedures were individually specific for the quantification of plasma carbamazepine.
The following articles in journals at HighWire Press have cited this article:
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T. Tomson Interdosage Fluctuations in Plasma Carbamazepine Concentration Determine Intermittent Side Effects Arch Neurol, August 1, 1984; 41(8): 830 - 834. [Abstract] [PDF] |
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