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出 处:《分析测试学报》2010年第3期276-279,共4页Journal of Instrumental Analysis
摘 要:建立了固相萃取/高效液相色谱法测定肝癌细胞中多西紫杉醇浓度的方法。细胞样品经三氯乙酸沉淀蛋白,Bond—elutC18固相萃取柱提取,采用AgilentTC—C18(5μm,4.6mm×150mm)色谱柱分析,以乙腈-0.02mol/L醋酸铵缓冲液(体积比50:50,醋酸调至pH5.0)为流动相,流速为1mL/min,检测波长为230nm,进样体积为20止。多西紫杉醇的质量浓度在0.05~2.25mg/L范围内线性关系良好,相关系数r=0.9993,检出限为0.03mg/L,提取回收率为93%~95%,其日内、日间精密度(n=5)不大于6.9%,且稳定性良好。方法简便、快速、灵敏度高、干扰小,可用于生物样品中低浓度多西紫杉醇的测定。To establish a high performance liquid chromatographic (HPLC) method for determination of docetaxel in hepatocellular cancer cells. Docetaxel was extracted from hepatocellular cancer cells by a Bond-elut C18 solid phase extraction(SPE) column, and separated on a Agilent TC-C18 (5 μm,4.6mm×150mm) column by using mobile phase consisted of ammonium acetate buffer(0. 02 mol/ L, pH 5.0) - acetonitrile(50 : 50, by volume) with a flow rate of 1 mL/min at detection wavelength of 230 nm. The result indicated that the calibration of docetaxel was linear in the range of 0. 05 - 2. 25 mg/L with correlation coefficient of 0. 999 3. The detection limit for docetaxel was 0. 03 mg/L. The extraction recoveries of docetaxel form forin cells sample ranged from 93% to 95%. The within-day RSDs(n = 5) and the between-day RSDs ( n = 5 ) were both not more than 6.9%. The method was convenient, accurate and sensitive, and could be applied in the determination of low level of docetaxel in biological samples.
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