摘要
样品中的虫草素、尿苷和腺苷用纯水经水浴80℃/30min提取,采用CALESILODS-100C18柱(5μm,4.6×250mm),在流动相为10mmol/LKH2PO3缓冲液(pH=6.0)∶甲醇=85∶15的色谱条件下分离,紫外260nm下检测。结果显示,虫草素、尿苷和腺苷的检测限分别为0.02μg/mL、0.01μg/mL和0.01μg/mL(以进样浓度计);方法的相对标准偏差分别为1.8%、0.68%和0.10%;方法的加标回收率分别为96.7%、96.4%和99.4%。实验所建立的方法简便、快速、结果准确、可靠,能应用于虫草制品中虫草素、尿苷和腺苷含量的测定。
The cordycepin, uridine and adenosine in CALESIL ODS -100 Cls column (5μm,4.6 ×250 mm) samples were extracted by water at 80oC, separated with 10mmoL/L monopotassium phosphate( pH = 6.0) , methanol(85: 15,V/V) in mobile phase, and detected at UV 260nm. The detection limit of the three components was 0.02μg/mL, 0. 01μg/mL and 0. 01μg/mL ( count by concentration of sample injection). The recovery rates were 96.7% and 96.4% and 99.4%. Relative standard deviation were 1.8% and 0.68% and 0. 10%. The method is simple,quick, accurate and can be applied for detection of cordycepin and Uridine and adenosine in foods.
出处
《食品与发酵工业》
CAS
CSCD
北大核心
2010年第9期143-147,共5页
Food and Fermentation Industries
基金
2008年浙江省分析测试基金资助项目
关键词
HPLC
保健食品
虫草素
尿苷
腺苷
high performance liquid chromatograph, health foods, cordycepin, uridine, adenosine