首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simple and sensitive method for quantification of fludarabine triphosphate intracellular concentration in leukemic cells using isocratic liquid chromatography
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Simple and sensitive method for quantification of fludarabine triphosphate intracellular concentration in leukemic cells using isocratic liquid chromatography

机译:用等度液相色谱法测定白血病细胞中氟达拉滨三磷酸细胞内浓度的简单而灵敏的方法

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摘要

A simple, isocratic HPLC method was newly developed for quantitating intracellular fludarabine triphosphate (F-ara-ATP). Samples (500 μl) were injected onto an anion-exchange column and eluted isocratically with phosphate-acetonitrile buffer (flow rate: 0.7 ml/min) at an ambient temperature. F-ara-ATP was quantitated according to its peak area at the absorbance of 261 nm. The standard curve was linear with minimal within-day and inter-day variability. The low and high quantification limits were 50 pmol and 20 nmol, respectively. The method was capable of measuring F-ara-ATP generated in cultured leukemic cells in vitro. Thus, our method will be useful because of its sensitivity and simplicity as well as applicability to biological materials.
机译:新开发了一种简单的等度HPLC方法,用于定量细胞内三磷酸氟达拉滨(F-ara-ATP)。将样品(500μl)注入到阴离子交换柱上,并在环境温度下用磷酸盐-乙腈缓冲液(流速:0.7 ml / min)等度洗脱。根据其在261 nm吸光度处的峰面积对F-ara-ATP进行定量。标准曲线是线性的,日内和日间波动最小。定量下限和下限分别为50 pmol和20 nmol。该方法能够测量体外培养的白血病细胞中产生的F-ara-ATP。因此,我们的方法由于其灵敏性和简单性以及对生物材料的适用性而将是有用的。

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