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[高效液相色谱法测定壮药大头艾纳香中的三种化学成分]

[Determination of three chemical constituents in zhuang medicine Blumea megacephala (Randeria) by HPLC].

作者信息

Ning Xiaoqing, Li Yaohua, Tan Yuanfeng, Chen Yong, Huang Yan, Pan Fuqi

机构信息

Guangxi College of Traditional Chinese Medicine, Nanning 530001, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2011 Jun;36(12):1623-5.

PMID:22007547
Abstract

OBJECTIVE

To develop an HPLC method for content determination of protocatechuic acid, chlorogenic acid and caffeic acid in Zhuang medicine Blumea megacephala (Randeria), and explore the content variation of the 3 components of the herbs harvesting in different months, and provide the scientific basis of reasonable application.

METHOD

The determination was carried out on a Shimadzu VP-ODS column (4.6 mm x 250 mm, 5 microm) eluted with acetonitrile and water containing 0.1% phosphoric acid in a linear gradient elution. The flow rate was 1 mL min(-1), and the detected wavelength was set at 258, 327nm.

RESULT

The peak areas and the concentrations of the three components had good linear relationship in the range of 1.7-17 mg x L(-1) for protocatechuic acid, 15.6-156 mg x L(-1) for chlorogenic acid, 3.96-39.6 mg x L(-1) for caffeic acid. The average recoveries were 103.4%, 102.2%, 98.5%, respectively.

CONCLUSION

The method was proved to be simple, accurate and used for the quality evaluation of Blumea megacephala (Randeria).

摘要

目的

建立高效液相色谱法测定壮药大头艾纳香中原儿茶酸、绿原酸和咖啡酸的含量,探讨不同月份采收的药材中这3种成分的含量变化情况,为合理用药提供科学依据。

方法

采用岛津VP-ODS柱(4.6 mm×250 mm,5μm),以乙腈和含0.1%磷酸的水为流动相进行线性梯度洗脱。流速为1 mL·min⁻¹,检测波长设定为258、327 nm。

结果

原儿茶酸在1.7 - 17 mg·L⁻¹、绿原酸在15.6 - 156 mg·L⁻¹、咖啡酸在3.96 - 39.6 mg·L⁻¹范围内,3种成分的峰面积与浓度呈良好的线性关系。平均回收率分别为103.4%、102.2%、98.5%。

结论

该方法简便、准确,可用于大头艾纳香的质量评价。

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