TY - JOUR T1 - Development of Four-Probe Drugs Cocktail Approach Evaluating Major Drug Metabolizing Enzymes Activity AU - , Guang-Tao Yao AU - Chen, Hua-Ying AU - , Feng-Jie Li AU - , Sheng-Guang Fu AU - , Ruo-Min Jin JO - Journal of Animal and Veterinary Advances VL - 11 IS - 9 SP - 1405 EP - 1410 PY - 2012 DA - 2001/08/19 SN - 1680-5593 DO - javaa.2012.1405.1410 UR - https://makhillpublications.co/view-article.php?doi=javaa.2012.1405.1410 KW - HPLC KW -cytochrome P450 KW -Cocktail Method KW -probe drug KW -dapson KW -sensitive AB - A simple, fast and sensitive HPLC Method was developed for the simultaneous quantification of phenacetin, dapson, omeprazole and chlorzoxazone, reflecting the activities of CYP1A2, CYP3A4, CYP2C19 and CYP2E1 isozyme, respectively. HPLC analyses were performed on a reverse phase C18 column (5 μm, 4.6x250 mm) operating at 30°C. The mobile phase consisted of a acetonitrile and phosphate buffer (pH 6.4-6.5, 34:66). The eluate was detected at 280 nm and the retention times for each compound were within 10 min. The method was validated over the concentration ranges 0.25-25 μg mL-1 for dapson, omeprazole and chlorzoxazone, 0.5-25 μg mL-1 for phenacetine. The intra and inter day precisions were 0.88-5.80 and 3.26-7.75%, respectively and the accuracy ranged from 94.17-103.74 and 93.45-107.08%. The Limit of Quantification (LOQ) was 0.25 μg mL-1 for dapson, omeprazole and chlorzoxazone, 0.5 μg mL-1 for phenacetin. The present method provided a robust, fast and sensitive analytical approach for the four cytochrome P450 probe drug cocktail. ER -