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引用本文:黄盼盼,马临科,唐登峰,赵维良.HPLC测定绞股蓝中七叶胆苷XLVI和人参皂苷Rb3含量[J].中国现代应用药学,2019,36(12):1529-1532.
HUANG Panpan,MA Linke,TANG Dengfeng,ZHAO Weiliang.Determination of Gypenoside XLVI and Ginsenoside Rb3 in Gynostemma pentaphyllum by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2019,36(12):1529-1532.
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HPLC测定绞股蓝中七叶胆苷XLVI和人参皂苷Rb3含量
黄盼盼1, 马临科2, 唐登峰2, 赵维良2
1.浙江中医药大学, 杭州 310053;2.浙江省食品药品检验研究院, 杭州 310052
摘要:
目的 建立HPLC测定绞股蓝中七叶胆苷XLVI和人参皂苷Rb3含量的方法。方法 采用Ultimate XB-C18色谱柱(250 mm×4.6 mm,5 μm),以乙腈(A)-水(B)线性梯度洗脱,检测波长203 nm,流速1 mL·min-1,柱温30℃。结果 七叶胆苷XLVI在3.30~39.62 μg·mL-1范围内线性良好(r2=0.999 7),平均回收率为113%,RSD为1.84%;人参皂苷Rb3在3.27~39.26 μg·mL-1范围内线性良好(r2=0.999 7),平均回收率为102%,RSD为2.82%。结论 该方法有较好的分离效果,准确性、精密度和重复性良好,为绞股蓝的研究和质量控制提供了科学依据。
关键词:  绞股蓝  七叶胆苷XLVI  人参皂苷Rb3
DOI:10.13748/j.cnki.issn1007-7693.2019.12.015
分类号:R284.1
基金项目:浙江省食品药品安全"十三五"规划-中药材数字标本馆(浙食检z-2016001)
Determination of Gypenoside XLVI and Ginsenoside Rb3 in Gynostemma pentaphyllum by HPLC
HUANG Panpan1, MA Linke2, TANG Dengfeng2, ZHAO Weiliang2
1.Zhejiang Chinese Medicine University, Hangzhou 310053, China;2.Zhejiang Institute of Food and Drug Control, Hangzhou 310052, China
Abstract:
OBJECTIVE To establish a reversed phase HPLC for simultaneous determination of gypenoside XLVI and ginsenoside Rb3 in Gynostemma pentaphyllum. METHODS The separation of gypenoside XLVI and ginsenoside Rb3 were performed on a Ultimate XB-C18 (250 mm×4.6 mm, 5 μm) with methanol(A)-water(B) as mobile phase in a gradient elution program at a flow rate of 1 mL·min-1. The column temperature was maintained at 30℃. The detection wavelength was 203 nm. RESULTS Gypenoside XLVI and ginsenoside Rb3 showed a good linearity range in 3.30-39.62 μg·mL-1 (r2=0.999 7) and 3.27-39.26 μg·mL-1 (r2=0.999 7), respectively. The average recoveries were 113% and 102%, RSD were 1.84% and 2.82%, respectively. CONCLUSION This method is accurate with high simplify, stability, and reliability, and can be used for quality research of Gynostemma pentaphyllum.
Key words:  Gynostemma pentaphyllum (Thunb.) Mak.  gypenoside XLVI  ginsenoside Rb3
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