Abstract
Object: To Study the pharmacokinetics and metabolism of Sodium 7,4' -oxo-acetic acid daidzein in rat.
Method: Sodium 7,4' -oxo-acetic acid daidzein was determined by reversed-phase HPLC (column: German CenturySIL BDS C18 5μm silica, 200mm×4.6mm i.d; fluid: methanol-water-85% phosphoric acid(57:43:0.05, v/v/v)), with sodium benzoic acid as an internal standard. Biological samples were extracted with acetonitrile. Results: The calibration curve was linear over the range of 1.0-1000μg/ml in rat plasma, urine and feces. The average extraction recoveries were 73.3% (plasma), 73.9% (urine) and 83.7% (feces) respectively and the intra-day and inter-day precisions were less than 8.34%. The assay was applied to the analysis of samples from a pharmacokinetic study. The absolute bioavailability of oral administration was 3.07%. DZ I original compound determined in 6h urine was 32.32%, in 24h urine was 32.71%, in 24h feces was 22.96%.Keywords: DZ I, pharmacokinetics, metabolism, rat, plasma, urine, feces
Drug Metabolism Letters
Title:The Pharmacokinetics and Metabolism Study of Sodium 7,4' -oxo-acetic Acid Daidzein in Rat
Volume: 6 Issue: 2
Author(s): Shujun Wang, Ruixue Gao, Kun Xu, Xiaojun Yi, Wei Hou, Chengyu Liu and Fei Cheng
Affiliation:
Keywords: DZ I, pharmacokinetics, metabolism, rat, plasma, urine, feces
Abstract: Object: To Study the pharmacokinetics and metabolism of Sodium 7,4' -oxo-acetic acid daidzein in rat.
Method: Sodium 7,4' -oxo-acetic acid daidzein was determined by reversed-phase HPLC (column: German CenturySIL BDS C18 5μm silica, 200mm×4.6mm i.d; fluid: methanol-water-85% phosphoric acid(57:43:0.05, v/v/v)), with sodium benzoic acid as an internal standard. Biological samples were extracted with acetonitrile. Results: The calibration curve was linear over the range of 1.0-1000μg/ml in rat plasma, urine and feces. The average extraction recoveries were 73.3% (plasma), 73.9% (urine) and 83.7% (feces) respectively and the intra-day and inter-day precisions were less than 8.34%. The assay was applied to the analysis of samples from a pharmacokinetic study. The absolute bioavailability of oral administration was 3.07%. DZ I original compound determined in 6h urine was 32.32%, in 24h urine was 32.71%, in 24h feces was 22.96%.Export Options
About this article
Cite this article as:
Wang Shujun, Gao Ruixue, Xu Kun, Yi Xiaojun, Hou Wei, Liu Chengyu and Cheng Fei, The Pharmacokinetics and Metabolism Study of Sodium 7,4' -oxo-acetic Acid Daidzein in Rat, Drug Metabolism Letters 2012; 6 (2) . https://dx.doi.org/10.2174/1872312811206020145
DOI https://dx.doi.org/10.2174/1872312811206020145 |
Print ISSN 1872-3128 |
Publisher Name Bentham Science Publisher |
Online ISSN 1874-0758 |