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[高效液相色谱法测定菠萝叶中的1,3-O-二咖啡酰甘油酯]

[Determination of 1, 3-O-dicaffeoylglycerides from leaves of pineapple by HPLC].

作者信息

Shen Jia, Xie Wei-Dong, Wang Wei, Ding Yi, Du Li-Jun

机构信息

Laboratory of Pharmaceutical Sciences, Department of Biological Science and Biotechnology, Tsinghua University, Beijing 100084, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2007 May;32(9):813-5.

Abstract

OBJECTIVE

To establish a HPLC method for a new compound 1,3-O-dicaffeoylglycerides determination.

METHOD

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.

RESULT

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.

CONCLUSION

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.

摘要

目的

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。

方法

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℃。

结果

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%。

结论

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。

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