摘要
目的:建立细胞内外酒石酸长春瑞滨含量浓度的高效液相色谱测定方法。方法:色谱柱,LichrospherC18(4.6mm×250mm,5μm);流动相:磷酸盐缓冲液(0.05 mol/ml的磷酸二氢钾,pH 3.5):乙腈=70∶30(v/v);柱温为30℃;检测波长269 nm;流速为1 ml/min;进样体积为10μl。结果:酒石酸长春瑞滨在0.5~25μg/ml范围内线性关系良好,细胞外液的平均提取回收率为84.6%,平均加样回收率为100.3%,日内、日间RSD≤4.84%;细胞内液平均提取回收率为88.2%,平均加样回收率为98.3%,日内、日间RSD≤4.69%;最低检测限0.1μg/ml。结论:本法简单、快速、选择性好,适合酒石酸长春瑞滨含量的测定。
Objective:To establish an HPLC method for the determination of vinorelbine tartrate in and out of cells.Methods:The vinorelbine tartrate was frozen and defrosted time and again.Then the sample was extracted with methanol and determined through Lichrospher C18(4.6 mm×250 mm,5 μm)column in a mobile phase of 50 mmol/ml potassium phosphate buffer(pH 3.5) and acetonitrile(70:30 v/v) with the flow rate of 1.0 ml/min at 30℃.The detection wavelength was 269 nm.Result: It was accurate and sensitive with a linear range from 0.5 μg/ml to 25 μg/ml for Vinorelbine Tartrate.The mean extraction recovery of extracellular fluid obtained was 84.6%,and the absolute recovery was 100.3%.Intra-and inter day periods expressed as percent R.S.D.were≤4.84%.For intracellular fluid,the mean extraction recovery was 88.2% and the absolute recovery was 98.3%.Intra and inter day periods expressed as percent R S D were≤4.69%.The lowest limit of quantification was 0.5 μg/ml.Conclusion:This method is simple,rapid,accurate and selective for the determination of VCR.
出处
《重庆医科大学学报》
CAS
CSCD
北大核心
2011年第3期332-334,355,共4页
Journal of Chongqing Medical University