Shen Jia, Xie Wei-Dong, Wang Wei, Ding Yi, Du Li-Jun
Laboratory of Pharmaceutical Sciences, Department of Biological Science and Biotechnology, Tsinghua University, Beijing 100084, China.
Zhongguo Zhong Yao Za Zhi. 2007 May;32(9):813-5.
To establish a HPLC method for a new compound 1,3-O-dicaffeoylglycerides determination.
The separation was performed in a Kromasil C18 column (4.6 mm x 150 mm, 5 microm) with a mobile phase of 0.1% H3PO4: Acetontrile = 75 : 25 (v/v). The flow rate was 1.0 ml x min(-)1 and the temperature of column was 30 degrees C.
A satisfactory separation between 1, 3-O-dicaffeoylglycerides and impurity was obtained. The calibration curve was linear over the concentration range from 0.051 6 microg to 0.516 microg, r = 0.999 9. The average recoveries was 97.1% (RSD 1.3%). The content of 1,3-O-dicaffeoylglycerides in pineapple leaves from three different batches were 0.033%, 0.034% and 0.031% respectively.
The method has good selectivity, high recovery and reproducibility, and can be used for the analysis of 1,3-O-dicaffeoylglycerides in pineapple leaves and their quality control.
建立一种用于测定新化合物1,3 - O - 二咖啡酰甘油酯的高效液相色谱法。
采用Kromasil C18柱(4.6 mm×150 mm,5μm)进行分离,流动相为0.1% H3PO4:乙腈 = 75 : 25(v/v)。流速为1.0 ml·min⁻¹,柱温为30℃。
1,3 - O - 二咖啡酰甘油酯与杂质之间实现了良好的分离。校准曲线在0.051 6μg至0.516μg浓度范围内呈线性,r = 0.999 9。平均回收率为97.1%(相对标准偏差1.3%)。来自三个不同批次菠萝叶中1,3 - O - 二咖啡酰甘油酯的含量分别为0.033%、0.034%和0.031%。
该方法具有良好的选择性、高回收率和重现性,可用于菠萝叶中1,3 - O - 二咖啡酰甘油酯的分析及其质量控制。