首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Determination of 5-fluorouracil in microvolumes of human plasma by solvent extraction and high-performance liquid chromatography
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Determination of 5-fluorouracil in microvolumes of human plasma by solvent extraction and high-performance liquid chromatography

机译:溶剂萃取和高效液相色谱法测定人血浆中的5-氟尿嘧啶

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摘要

In the present study,a new reversed-phase HPLC method has been developed and validated for the quantitative determination of 5-fluorouracil (5-FU) in human plasma using only 100-#mu#l samples. The sample extraction and clean-up procedure involved a simple liquid-liquid extraction after addition of 5-chlorouracil (5-CU),used as internal standard,with 5 ml ethyl acetate. Chromatographic separations were performed on an Inertsil ODS-3 column (250×4.6 mm ID;5 #mu#M particle size),eluted with a mobile phase composed of acidified water (pH 2.0). The column effluent was monitored by UV absorption measurement at a wavelength of 266 nm. The calibration curves were constructed over a rangef of 0.20-50.0 #mu#M and were fitted by weighted (1/x) linear regression analysis using the ratio of peak heights of 5-FU and 5-CU versus concentrations of the nominal standards. Extraction recoveries over the total range averaged 92 and 93% for 5-FU and 5-CU,respectively. The lower limit of quantitation was established at 0.20 #mu#M (approx26 ng/ml), with within-run and between-run precisions of 4.2 and 7.0%,respectively,and an average accuracy of 109.3%. The within-run and between-run precisions at four tested concentrations analyzed in quintuplicate over a time period of four days were <1.4 and <4.4%,respectively. The accuracy at the tested concentrations ranged from 98.4 to 102.3%. Compared to previously described validated analytical methods for 5-FU, our present assay provides equivalent to superior sensitivity using only microvolumes of sample.
机译:在本研究中,已开发出一种新的反相HPLC方法,并已验证该方法仅使用100-#mu#l样品即可定量测定人血浆中的5-氟尿嘧啶(5-FU)。样品提取和净化过程涉及在添加5-氯尿嘧啶(5-CU)(用作内标)后,用5 ml乙酸乙酯进行简单的液-液提取。色谱分离是在Inertsil ODS-3色谱柱(250×4.6 mm内径; 5#mu#M粒径)上进行的,用酸性水(pH 2.0)组成的流动相洗脱。通过UV吸收测量在266nm的波长监测柱流出物。在0.20-50.0#mu#M的范围内构建校准曲线,并使用5-FU和5-CU的峰高与名义标准浓度之比通过加权(1 / x)线性回归分析进行拟合。 5-FU和5-CU的总回收率分别平均为92%和93%。定量下限为0.20#μM(约26 ng / ml),批内和批间精密度分别为4.2%和7.0%,平均准确度为109.3%。在四天的时间内,一式四份地分析的四个测试浓度的批内和批间精密度分别为<1.4和<4.4%。在测试浓度下的准确度为98.4%至102.3%。与先前描述的经过验证的5-FU分析方法相比,我们目前的分析方法仅使用微量样品就可提供等同于卓越的灵敏度。

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