基于高灵敏度荧光衍生剂的痕量维生素C液相检测方法建立
Determination of Trace Vitamin C in Liquid Phase Based on High Sensitivity Fluorescence Derivative
-
摘要: 利用1.0 g/L 6-羟基-2,4,5-三氨基嘧啶作为荧光衍生剂,与水溶液中维生素C在pH为6.5±0.5反应条件下,40 ℃衍生反应30 min生成具有强荧光性的衍生产物。试验中对维生素C提取条件,衍生条件,色谱条件进行探索性研究及优化。在使用pH=4.0乙酸铵缓冲液(v)+乙腈(v)+甲醇(v)=80+15+5作为流动相的色谱条件下,该衍生物色谱行为稳定,并产生很强的荧光信号。配合高效液相色谱-荧光检测器对其含量进行检测。该方法检测维生素C具有检测结果准确,回收率为90.9%~96.7%,实验数据稳定RSD≤2%,灵敏度高方法检出限0.2 μg/g,检测线性范围0.05~500 μg/g,相关性系数良好,y=93322x-1837.8,R2=0.9999,实验操作简便,无需重复制备空白样品操作等特点,更适合实验室批量检测任务。并对6-羟基-2,4,5-三氨基嘧啶作为荧光衍生剂的使用提供一定的参考。Abstract: Using 1.0 g/L 6-hydroxy-2,4,5-traminopyrimidine as the fluorescence derivative,the derivatives with strong fluorescence were generated at 40 ℃ for 30 min under the condition of reaction with vitamin C in aqueous solution at a pH of 6.5±0.5.The extraction,derivation and chromatographic conditions of vitamin C were studied and optimized. Under the condition of using pH=4.0 ammonium acetate buffer(v)+ acetonitrile(v)+ methanol(v)=80+15+5 as the mobile phase,the derivative had stable chromatographic behavior and generates a strong fluorescence signal. Its content was detected by high performance liquid chromatography-fluorescence detector. Vitamin C with accurate result,the method recovery was 90.9%~96.7%,experimental data RSD≤2% or less stable,high sensitivity method detection limit of 0.2 μg/g,detection of linear range 0.05~500 μg/g,good correlation coefficient,y=93322x-1837.8,R2=0.9999,experimental operation was simple,did’t need to repeat the preparation of blank sample operation and other characteristics,was more suitable for laboratory batch testing tasks. Some references were provided for the use of 6-hydroxy-2,4,5-traminopyrimidine as a fluorescence derivative.