摘要
目的分析测定芒果苷原料药中高芒果苷的含量。方法采用C18柱(大连依利特分析仪器有限公司,Hypersil ODS 5μm,4.6mm×250mm),流动相为甲醇-0.1%磷酸(32:68),流速1ml/min,检测波长258nm。结果高芒果苷在0.0424-0.848μg范围内进样量与峰面积呈良好的线性关系(r=0.9999),平均回收率为97.8%,RSD=2.2%(n=6)。结论该方法简便,灵敏,重复性好,可作为芒果苷原料药中高芒果苷的含量测定方法。
Objective To determine Homomangiferin in raw medicine of Mangiferin by HPLC. Methods Homomangiferin was separated on Hypersil ODS 5μm column (4.6 mmID × 250mm) with a mobile phase of methanol -0. 1% phosphoric acid solution (32:68 ) and detected at a wavelength of 258 nm. Results The calibration curve was linear in the range of 0.042 4 - 0. 848 μg (r = 0.999 9). The average recovery rate was 97.8% and RSD = 2.2% (n = 6). Conclusion The method is simple, sensitive and precise. It can be used for the determination of Homomangiferin in raw medicine of Mangifierin.
出处
《时珍国医国药》
CAS
CSCD
北大核心
2008年第6期1295-1296,共2页
Lishizhen Medicine and Materia Medica Research
基金
国家科技部重大项目资助课题(No.2004BA901A09)
广西科技厅科技创新能力与条件建设项目(No.桂科能0630006-5A)
关键词
高芒果苷
芒果苷原料药
高效液相色谱
Raw medicine of Mangiferin
The content of Homomangiferin
HPLC