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[反相高效液相色谱法测定乌药中去甲异波尔定的含量]

[Determination of norisoboldine in Radix Lindera by RP-HPLC].

作者信息

Chen Jianzhong, Chou Guixin, Yang Li, Wang Changhong, Wang Zhengtao

机构信息

Department of Pharmacognosy, China Pharmaceutical University, Nanjing 210038, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2009 Nov;34(21):2774-6.

PMID:20209913
Abstract

OBJECTIVE

To develop a RP-HPLC method for quantitative determination of norisoboldine in Radix Linderae and to provide valuable data for quality control of Radix Linderae.

METHOD

The separation was performed on a Phenomenex Gemini C18 column (4.6 mm x 250 mm, 5 microm) at 25 degrees C using a gradient elution of mobile phase A (0.5% formic acid, adjusted pH 2.25 with triethylamine) and mobile phase B (acetonitrile). The detection wavelength was 280 nm.

RESULT

The calibration curve showed a good linearity (r = 0.999 9) within test ranges of 0.015-1.509 microg. The average recovery was 99.58% with RSD 1.4%.

CONCLUSION

The developed method is simple, accurate and reliable with good repeatability. It is suitable for quality evaluation of Radix Linderae.

摘要

目的

建立一种反相高效液相色谱法(RP-HPLC)用于定量测定乌药中的去甲异波尔定,并为乌药的质量控制提供有价值的数据。

方法

采用菲罗门Gemini C18柱(4.6 mm×250 mm,5μm),在25℃下进行分离,流动相A(0.5%甲酸,用三乙胺调pH至2.25)和流动相B(乙腈)进行梯度洗脱。检测波长为280 nm。

结果

在0.015 - 1.509μg的测试范围内,校准曲线呈现良好的线性关系(r = 0.999 9)。平均回收率为99.58%,相对标准偏差(RSD)为1.4%。

结论

所建立的方法简便、准确、可靠,重复性良好。适用于乌药的质量评价。

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