Development of a simplified, sensitive high-performance liquid chromatographic method using fluorescence detection to determine the concentration of UCN-01 in human plasma

被引:3
作者
Smith, JA
Cortes, J
Newman, RA
Madden, TL
机构
[1] Univ Texas, MD Anderson Canc Ctr, Div Pharm, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Div Canc Med, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Pharmaceut Dev Ctr, Houston, TX 77030 USA
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 760卷 / 02期
关键词
UCN-01;
D O I
10.1016/S0378-4347(01)00276-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
UCN-01 is a naturally derived anticancer agent isolated in the culture broth of actinomyces streptomyces. We have developed a sensitive high-performance liquid chromatographic method for the determination of UCN-01 in human plasma. UCN-01 was isolated from human plasma after intravenous administration, by using 100% ice-cold acetonitrile liquid-liquid phase extraction. Liquid chromatographic separation was achieved by isocratic elution on a phenyl analytical column. The mobile phase consisted of acetonitrile-0.5 M ammonium acetate (45:55) with 0.2% triethylamine added as a modifier. The UCN-01 peak was identified from other peaks using fluorescence excitation energy and emission energy wavelengths of 310 and 410 nm, respectively. Retention time for UCN-01 was 4.2 +/-0.5 min. The UCN-01 peak was baseline resolved, with nearest peak at 2.6 min distance. No interfering peaks were observed at the retention time of UCN-01. Peak area amounts from extracted samples were proportional over the dynamic concentration range used: 0.2 to 30 mug/ml. Mean recoveries of UCN-01 at concentrations of 0.5 and 25 mug/ml were 89 and 90.2%, respectively. Relative standard deviations for UCN-01 calibration standards ranged from 1.89 to 2.31%, with relative errors ranging from 0.3 to 11.6%. Assay precision for UCN-01 based on quality control samples of 0.50 mug/ml was +/-4.86% with an accuracy of +/-5.7%. For drug extracted from plasma the lowest limit of detection was 0.1 mug/ml, with the lowest limit of quantitation being 0.2 mug/ml. This method is suitable for routine analysis of UCN-01 in human plasma at concentration from 0.2 to 30 mug/ml. (C) 2001 Elsevier Science BV All rights reserved.
引用
收藏
页码:247 / 253
页数:7
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