摘要
目的建立测定水解后的川木通药材中齐墩果酸含量的方法。方法采用HPIE法。Alltima C18色谱柱(250mm×4.6mm,5μm);流动相为甲醇-水-冰醋酸-三乙胺(89:11:0.04:0.02);检测波长207nm;流速1.0ml·min^-1;柱温45℃。结果齐墩果酸色谱峰分离度良好,线性范围为0.1003—8.024μg(r=0.9999,n=5),方法的检测限和定量限分别为0.3μg·ml^-1和1.0μg·ml^-1。平均回收率为96.1%,RSD=2.8%(n=5)。结论所用结果准确,重复性好,专属性强,可为川木通药材质量控制提供科学的依据。
OBJECTIVE To develop an HPLC method for the content determination of oleanolic acid in Caulis clematidis armandii after hydrulysis.METHODS In the system of HPLC, a AUtima C18(250 mm × 4.6 mm,5 μm) column was used with a mixture of methanol - water - acetic acid - triethylamine (89:11:0.04:0.02) as the mobile phase. The measuring wavelength was set at 207 rim. The flow rate was 1.0 ml· min ^-1 and the column temperature maintained at 45 ℃. RESULTS The oleanolic acid peak in chromatograms was completely separated from other peaks. The linear range of oleanolie acid was 0. 1003 - 8.024 μg ( r = 0. 9999, n = 5). The detection limit and quanfitation limit of this method were 0.3μg· ml^-1 and 1.0μg· ml^-1 respectively. The average recovery of oleanolic acid was 96.1% ( RSD = 2.8 %, n = 5). CONCLUSION The method is accurate, precise and reproducible. It can be used to evaluate the quality of Caulis clematidis armandii.
出处
《华西药学杂志》
CAS
CSCD
北大核心
2006年第3期273-274,共2页
West China Journal of Pharmaceutical Sciences
基金
国家教育部博士点基金资助(编号:20020610089)