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Publication Type : Journal Article
Thematic Areas : Wireless Network and Application
Publisher : Xenobiotica .
Source : Xenobiotica, vol. 33, no. 12, pp. 1233–1245, 2003
Keywords : 6 hydroxychlorzoxazone, 6beta hydroxytestosterone, accuracy, analytic method, article, bufuralol, calibration, celecoxib, Cells, chlorzoxazone, Chromatography, controlled study, coumarin, Cultured, Cytochrome P-450 Enzyme System, cytochrome P450, diazepam, diethyldithiocarbamic acid, disulfiram, drug metabolism, Fluorescence, furafylline, high performance liquid chromatography, High Pressure Liquid, human, human cell, Humans, hydroxybufuralol, hydroxytolbutamide, ketoconazole, liquid extraction, Lymphocytes, molecular probe, nordazepam, paracetamol, Pharmaceutical Preparations, phenacetin, Quality control, quinidine, Reproducibility of Results, reversed phase liquid chromatography, sensitivity and specificity, sulfaphenazole, testosterone, tolbutamide, tranylcypromine, umbelliferone, unclassified drug, validation process
Campus : Amritapuri
School : School of Engineering
Center : Amrita Center for Wireless Networks and Applications (AmritaWNA)
Department : Wireless Networks and Applications (AWNA)
Year : 2003
Abstract : An 'open access' generic high-performance liquid chromatography method was developed for different combination sets each containing specific cytochrome P450 probe substrate and the corresponding metabolite. Method development, optimization and validation were carried out with the following combinations: phenacetin + paracetamol + internal standard (IS, celecoxib), bufuralol + hydroxybufuralol + IS, testosterone + 6β-hydroxytestosterone + IS, chlorzoxazone + 6-hydroxychlorzoxazone + IS, coumarin + 7-hydroxycoumarin + IS, tolbutamide + hydroxytolbutamide + IS, and diazepam + desmethyldiazepam + IS. 2. The assay procedure involved a simple one-step liquid/liquid extraction followed by reverse phase chromatography (Inertsil ODS 3V column) employing a ternary gradient system and the eluate was monitored by a photodiode array/fluorescence detector. The standard curve for each compound, in the concentration range 0.1-10 μg ml-1, in various sets was linear (r2 gt; 0.99) and absolute recoveries of all analytes were gt; 90%. The lower limit of quantification was 0.1 μg ml-1. The intraday precision and accuracy in the measurements of quality control were lt; 15% relative standard deviation and lt; 15% deviation from nominal values, respectively. 3. Each combination set was tested with individual chemical inhibitors (furafylline, quinidine, ketoconazole, disulfiram, diethyldithiocarbamate, sulphaphenazole and tranylcypromine) and all analytes were well resolved. Overall, the assay is simple, uses conventional instrumentation and provides a scope to analyse all cytochrome P450 combination sets continuously. The application of the method in the cytochrome P450 liability screen of novel compounds is also presented.
Cite this Research Publication : N. V. S. M Rao, Biju, B., Ansar, A. K., Mujeeb, S., Dr. Maneesha V. Ramesh, and Srinivas, N. R., “‘Open Access’ Generic Method for Continuous Determination of Major Human CYP450 Probe Substrates/Metabolites and its Application in Drug Metabolism Studies”, Xenobiotica, vol. 33, no. 12, pp. 1233–1245, 2003