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论文摘要

UPLC测定纤毛婆婆纳主要环烯醚萜苷成分的含量

Study on the content determination of main iridoid glycosides in Veronica ciliata Fisch by UPLC

作者:罗朝梅(四川大学生命科学学院 生物资源与生态环境教育部重点实验);卢秋霞(四川大学生命科学学院 生物资源与生态环境教育部重点实验);贺丽波(四川大学生命科学学院 生物资源与生态环境教育部重点实验);张士彦(四川大学生命科学学院 生物资源与生态环境教育部重点实验);孙意冉(四川大学生命科学学院 生物资源与生态环境教育部重点实验);唐琳(四川大学生命科学学院 生物资源与生态环境教育部重点实验)

Author:LUO Chao-Mei(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University);LU Qiu-Xia(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University);HE Li-Bo(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University);ZHANG Shi-Yan(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University);SUN Yi-Ran(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University);TANG Lin(Key Laboratory Bio-resources and Eco-environment of Ministry Education,College of Life Science, Sichuan University)

收稿日期:2018-10-09          年卷(期)页码:2019,56(5):971-975

期刊名称:四川大学学报: 自然科学版

Journal Name:Journal of Sichuan University (Natural Science Edition)

关键字:超高效液相色谱;纤毛婆婆纳;环烯醚萜苷;含量测定

Key words:UPLC; Veronica ciliata Fisch.; The iridoid glycosides; Content determination

基金项目:国家自然科学基金(31570351)

中文摘要

建立超高效液相色谱法(UPLC)同时测定纤毛婆婆纳中梓醇、梓苷、胡黄连苷Ⅱ和6-O-藜芦酰梓苷4种主要环烯醚萜苷类成分含量.采用Waters ACOUITY T3色谱柱(100 mm×2.1 mm,1.8 μm);柱温为40 ℃;流动相为乙腈-水(0.1%甲酸+2.5 mmol甲酸铵);流速为0.4 mL/min;检测波长为260 nm.结果表明梓醇、梓苷、胡黄连苷Ⅱ和6-O-藜芦酰梓苷4种主要环烯醚萜苷类成分含量.结果表明梓醇、梓苷、胡黄连苷Ⅱ和6-O-藜芦酰梓苷分别在1.562~50 μg/mL(R2=0.9987)、1.562~50 μg/mL(R2=0.9989)、4.689~143 μg/mL(R2=0.9996)、1.562~50 μg/mL(R2=0.9998)范围内呈现良好的线性关系,平均回收率分别为100.21%(RSD=1.3%)、99.43%(RSD=1.8%)、100.6%(RSD=2.5%)、102.7%(RSD=0.65%).该方法简便、灵敏、经济、可靠,可用于纤毛婆婆纳的质量控制和评价.

英文摘要

A UPLC method has been developed in the current investigation for simultaneous determination of four main iridoid glycosides, which were verproside, catalposide, amphicoside and 6-O-veratroylcatalposide in Veronica ciliata Fisch. The separation was performed at 40 ℃ on Waters ACOUITY T3 column (100 mm×2.1 mm, 1.8 μm); the mobile phase was acetonitrile-water(0.1% formic acid+2.5 mmol ammoniumformate); the flow rate was 0.4 mL/min and the detection wavelength was 260 nm. The results showed that the calibration curves were the good linear relationships in the range of 1.562~50 μg/mL (R2=0.9987) for verproside, 1.562~50 μg/mL (R2=0.9989) for catalposide, 4.689~143 μg/mL (R2=0.9996) for amphicoside, 1.562~50 μg/mL (R2=0.9998) for 6-O-veratroylcatalposide, the average recovery rate were 100.21%(RSD=1.3%), 99.43% (RSD=1.8%), 100.6% (RSD=2.5%), 102.7% (RSD=0.65%),respectively. The method is simple, sensitive, economical and reliable, and can be used for quality control and evaluation of Veronica ciliata Fisch.

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