Shaanxi Institute for Food and Drug Control, Xi'an, P R China.
J Sep Sci. 2011 Nov;34(21):3023-8. doi: 10.1002/jssc.201100386. Epub 2011 Oct 12.
To separate and determine oleanolic acid and ursolic acid, a rapid and accurate HPLC using γ-CD as the mobile phase additive was developed. The effect of CD nature and concentration, and the acidity of the mobile phase on the chromatographic behavior of two bioactive triterpenes were systematically studied. Two bioactive triterpenes were completely separated (R = 3.11) on a Kromasil(®) C(18) column (150×4.6 mm id, 5 μm) with the mobile phase consisting of acetonitrile/0.1% phosphoric acid with 2 mM γ-CD as the mobile phase modifier (60:40, v/v). The flow rate was set at 1.0 mL/min and the eluent was detected at 210 nm for two bioactive triterpenes. The linearity of the method was excellent (r=0.9999) over the studied range of 6-300 μg/mL for oleanolic acid, and 12-600 μg/mL for ursolic acid. The LOD and LOQ were 1.5 and 5.0, 1.0 and 3.0 μg/mL for oleanolic acid and ursolic acid, respectively. The optimized method was successfully applied to separate and determine two bioactive triterpenes in five Chinese herbs. It is concluded that this method could be used for rapid and accurate qualitative and quantitative analysis of the two bioactive triterpenes in Chinese herbs.
为了分离和测定齐墩果酸和熊果酸,开发了一种使用γ-CD 作为流动相添加剂的快速准确的 HPLC 方法。系统研究了 CD 性质和浓度以及流动相酸度对两种生物活性三萜类化合物色谱行为的影响。在 Kromasil(®)C18 柱(150×4.6mm id,5μm)上,使用乙腈/0.1%磷酸,其中含有 2mM γ-CD 作为流动相修饰剂(60:40,v/v),可完全分离两种生物活性三萜类化合物(R=3.11)。流速设定为 1.0mL/min,两种生物活性三萜类化合物的洗脱液在 210nm 处检测。该方法在 6-300μg/mL 范围内对齐墩果酸的线性良好(r=0.9999),在 12-600μg/mL 范围内对熊果酸的线性良好。齐墩果酸和熊果酸的检出限和定量限分别为 1.5 和 5.0μg/mL,1.0 和 3.0μg/mL。优化后的方法成功应用于五种中草药中两种生物活性三萜类化合物的分离和测定。结论认为,该方法可用于中草药中两种生物活性三萜类化合物的快速准确定性和定量分析。