摘要
目的建立同时检测人参中人参皂苷Rgl、Re、Rbl的超高效液相色谱(UPLC)分析方法。方法采用wa.tersAcquityUPLCBEHC18色谱柱(1.7μm,50mm×2.1mm)、乙腈一水为流动相、柱温30%、检测波长203nm的色谱条件,同时分离测定人参皂苷Rgl、Re、Rbl。样品以甲醇为提取溶剂,经大孔吸附树脂柱除去基质干扰,取2μl注入UPLC。结果人参皂苷Rgl、Re、Rbl在10—100mg/L范围内呈良好的线性关系,加标回收率在92.1%。105.2%,所测定的相对标准偏差在2.02%~3.85%之间。结论该方法灵敏、快速,结果准确可靠,可为人参中人参皂苷检测提供可靠的分析方法。
Objective To develop an ultra performance liquid chromatographic (UPLC) method for the simultaneous de- termination of ginseng Rgl ,Re,Rbl contents in ginseng. Methods The extracts were separated on an Acquity UPLC BEH Cls ( 1.7μm,50 mm ×2. 1 mm) by mobile phase of acetonitrile - water with UV detector at a wavelength of 203 nm. The an- alytes in ginseng were extracted with methanol. The extract was cleaned up using resin cartridge. Injection volume was 2 μl. Results The linearity of ginseng Rgl, Re and Rbl contents was good in the range of 10 - 100 mg/L. The recovery of the method was 92. 1% - 105.2% , and relative standard deviation(RSD) was 2. 02% -3. 85%. Conclusion The method is accurate, quick and reliable.
出处
《中国卫生工程学》
CAS
2014年第1期49-51,共3页
Chinese Journal of Public Health Engineering
关键词
人参皂苷
人参
超高效液相色谱法
固相萃取
Ginsenoside contents
Ginseng
Ultra performance liquid chromatography
Solid phase extraction