Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1223884 | Journal of Pharmaceutical and Biomedical Analysis | 2008 | 5 Pages |
Abstract
A simple isocratic and stability-indicating HPLC method was developed and validated for the quantitative determination of anti-tumor agent fluorapacin and its pharmaceutical preparation. A Spherisorb ODS II C18 (250 mm Ã 4.6 mm, 5 μm) column was eluted with a mobile phase consisting of acetonitrile/water (85:15, v/v). The analyses were performed at 40 ± 1 °C with a flow rate of 1.0 mL/min and UV detection at 218 nm. The calibration curve was linear over a concentration range of 160-240 μg/mL with the correlation coefficient of 0.9997. The LOD and LOQ were determined to be 1.4 and 7.0 ng/mL, respectively. Average recoveries were 98.27% and 100.40% for fluorapacin API and its drug product with corresponding relative standard deviations (R.S.D.) of 0.41% and 0.30%, respectively. Good repeatability (precision and intermediate precision), accuracy and tolerability were obtained with R.S.D. of <1.0%. This specific and reliable method has been successfully applied for quality control of fluorapacin API and drug product.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Yimei Bao, Yuyu He, Xiaoying Xu, Xiaopeng Mo, Xiao Xu, Xiaobo Wang, Haoyun An,