中文摘要：

目的：建立石芽茶中山茶苷A的含量测定方法.方法：采用反相高效液相法,以XB-C18柱（4.6 mm×250mm,5μm）为分离柱,以乙腈-0.1%磷酸（20：80）为流动相,检测波长为330nm,柱温为室温.结果：山茶苷A在（20.2～323.2）μg/ml范围内,峰面积与其浓度呈良好线性关系（r=1.000）,平均回收率为98.8%,RSD为1.62%（n=6）.结论：该方法简便、准确、重复性好,可作为该药材含量测定方法.

英文摘要：

Objeetive To set up determination the contents of Camelliagenin A in Adinandra nitida. Methods RP - HPLC method was used, Chromatographic condition included XB- C18 （4. 6mm × 250mm, 5 （m） and the mobile phase consisting of acetonitrile -0. 1% phosphoric acid （20： 80） , with a detection wavelength of 330nm and the temperature to room temperature. Result The cal- ibration curves were linear in the range of 20. 2 - 323.2μg,/ml for Camelliagenin A, r = 1. 000, average recovery of Camelliagenin A was 98. 8%, RSD was 1.62% （n =6）. Conclusions The method is simple, accurate and repeatable, which applied in determina- tion of Camelliagenin A in Adinandra nitida.