摘要
[目的]建立反相高效液相色谱法,同时测定湿生扁蕾中有效成分当药黄素、当药醇苷含量。[方法]采用Kromasil-C18(250mm×4.6mm,5um)色谱柱,流动相甲醇和水(含0.04%H3PO4),在0~20min甲醇:水由40:60~63:37线性梯度洗脱,流速0.8ml/min,检测波长254ml,柱温30℃。[结果]当药黄素、当药醇苷2种有效成分都在17min内均达到基线分离,当药黄素、当药醇苷的线性范围分别是0.338~2.025ug(r=0.9995)、0.275~1.650ug(r=0.9995),加标回收率为103.30%(RSD=3.20%)、99.60%(RSD=2.70%)。[结论]该方法快速,结果准确、可靠。
[Objective] The research aimed to establish a quantitative determination method of swertisin and swertianolin in Gentiopsis palulosa(Munro) Ma by RP-HPLC. [Method] The sample were separated on the column of Kromasil-C18 (4.6 mm× 250 nm,5 um) which eluted with methanol and water (0.04% phosphoric acid) .The ratio of methanol and water increased from 40:60 to 63:37 in 20 min with detected wave-length at 254 nm,flow rate at 0.8 ml/min, colunm temperature at 30℃. [Result] Two effective components were base-isolated. The linear ranges of swertisin and swertianolin were 0.338 - 2.025ug( r = 0.999 5) ,0.275 - 1.650ug ( r = 0.999 5) respectively. Tile average recoveries were 103.30% ( RSD = 3.20% ) ,99.60% ( RSD .: 2.70% ). [Conclusion] The method was rapid, precise and reliable.
出处
《安徽农业科学》
CAS
北大核心
2008年第24期10520-10521,10523,共3页
Journal of Anhui Agricultural Sciences