LI Huihong, LI Min, GUAN Hongya, et al. Determination of Chlorogenic Acid and Catalpol in Modified Simiao Yong’an Decoction by Reversed Phase High-Performance Liquid Chromatography. [J]. (1):36-39(2023)
DOI:
LI Huihong, LI Min, GUAN Hongya, et al. Determination of Chlorogenic Acid and Catalpol in Modified Simiao Yong’an Decoction by Reversed Phase High-Performance Liquid Chromatography. [J]. (1):36-39(2023) DOI: 10.14009/j.issn.1672-2124.2023.01.007.
Determination of Chlorogenic Acid and Catalpol in Modified Simiao Yong’an Decoction by Reversed Phase High-Performance Liquid Chromatography
摘要
目的:建立反相高效液相色谱法测定加味四妙勇安汤浸膏中绿原酸和梓醇含量的方法。方法:色谱柱为Merck Purospher?STARLP RP-18 endcapped柱(250 mm×4.6 mm
5μm)
流速为1.0 mL/min
柱温为35℃。(1)绿原酸的色谱条件,流动相为乙腈-0.4%磷酸(V∶V=11∶89)
检测波长为327 nm。(2)梓醇的色谱条件,流动相A为乙腈,流动相B为0.1%磷酸,梯度洗脱(0~15 min
0.8%A;15~60 min
2%A)
检测波长为210 nm。结果:绿原酸在4.420~442.0μg/mL(r=0.999 8)范围内质量浓度与峰面积成良好线性关系;平均回收率为99.38%(RSD=1.26%)。梓醇在9.760~488.0μg/mL(r=0.999 9)范围内质量浓度与峰面积成良好线性关系,平均回收率为99.34%(RSD=1.43%)。绿原酸和梓醇的最低检测限分别为0.40和0.82 ng
OBJECTIVE: To establish the reversed phase high-performance liquid chromatography method for the determination of chlorogenic acid and catalpol in modified Simiao Yong’an decoction. METHODS: The chromatographic column was Merck Purospher? STARLP RP-18 endcapped column(250 mm×4.6 mm
5 μm)
the flow rate was 1.0 mL/min
the column temperature was 35 ℃.(1) The chromatographic conditions of chlorogenic acid were acetonitrile-0.4% phosphoric acid(V∶ V=11∶ 89) as mobile phase
and the detection wavelength was 327 nm.(2) The chromatographic conditions of catalpol were as follows
mobile phase A was acetonitrile
mobile phase B was 0.1% phosphoric acid
gradient elution(from 0 to 15 min
0.8%A; from 15 to 60 min
2%A)
and the detection wavelength was 210 nm. RESULTS: Chlorogenic acid showed a good linear relationship in the ranges of 4.420 μg/mL to 442.0 μg/mL(r=0.999 8)
the average recovery was 99.38%(RSD=1.26%). Catalpol showed a good linear relationship in the range of 9.760 μg/mL to 488.0 μg/mL(r=0.999 9)
the average recovery was 99.34%(RSD=1.43%). The minimum detection limits of chlorogenic acid and catalpol were 0.40 ng and 0.82 ng
and the quantitative limits were 1.20 ng and 2.44 ng
respectively. The precision RSD were 0.71%(n=6) and 0.45%(n=6)
respectively. CONCLUSIONS: The method has the advantages of simple operation
good separation effect
repeatability and high accuracy
which can be used for the quality evaluation of the extract of modified Simiao Yong’an decoction.