Bao Yimei, He Yuyu, Xu Xiaoying, Mo Xiaopeng, Xu Xiao, Wang Xiaobo, An Haoyun
ACEA Bio (Hangzhou) Co., Ltd., Building 3, West Lake Technical & Economic Park, 2# Xiyuan 5 Road, Sandun, Hangzhou 310030, China.
J Pharm Biomed Anal. 2008 Jan 7;46(1):206-10. doi: 10.1016/j.jpba.2007.09.018. Epub 2007 Sep 25.
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 C(18) (250 mm x 4.6 mm, 5 microm) column was eluted with a mobile phase consisting of acetonitrile/water (85:15, v/v). The analyses were performed at 40+/-1 degrees 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 microg/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.
开发并验证了一种简单的等度洗脱且具有稳定性指示作用的高效液相色谱法,用于定量测定抗肿瘤药物氟阿帕星及其药物制剂。使用Spherisorb ODS II C(18)(250 mm×4.6 mm,5 µm)色谱柱,以乙腈/水(85:15,v/v)组成的流动相进行洗脱。分析在40±1℃下进行,流速为1.0 mL/min,在218 nm处进行紫外检测。校准曲线在160 - 240 μg/mL的浓度范围内呈线性,相关系数为0.9997。检测限和定量限分别确定为1.4和7.0 ng/mL。氟阿帕星原料药及其药品的平均回收率分别为98.27%和100.40%,相应的相对标准偏差(R.S.D.)分别为0.41%和0.30%。获得了良好的重复性(精密度和中间精密度)、准确度和耐受性,R.S.D. <1.0%。这种特异性强且可靠的方法已成功应用于氟阿帕星原料药和药品的质量控制。