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引用本文:张昆艳,洪挺,王栋,简勇学,赵凯,黄建丽,杨毅生.HPLC同时测定细梗香草中2个专属性黄酮苷的含量[J].中国现代应用药学,2020,37(13):1570-1573.
ZHANG Kunyan,HONG Ting,WANG Dong,JIAN Yongxue,ZHAO Kai,HUANG Jianli,YANG Yisheng.Simultaneous Determination of Two Specific Flavonoid Glycosides in Lysimachia Capillipes Hemsl. by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2020,37(13):1570-1573.
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HPLC同时测定细梗香草中2个专属性黄酮苷的含量
张昆艳1,2, 洪挺1, 王栋3, 简勇学4, 赵凯4, 黄建丽4, 杨毅生1
1.江西省药品检验检测研究院, 江西省药品与医疗器械质量工程技术研究中心, 南昌 330029;2.江西中医药大学, 南昌 330004;3.江西省食品检验检测研究院, 江西国家果蔬产品及加工食品质量监督检验中心, 南昌 330001;4.江西欧氏药业有限责任公司, 江西 新余 338004
摘要:
目的 建立HPLC同时测定细梗香草中Quercetin-3-O-(2'',6''-di-O-α-rhamnopyranosyl)-β-galactopyranoside和Kaempferol-3-O-[2-glucopyranosyl (1→3)rhamnopyranosyl-6-rhamnopyranosyl]-β-D-galactopyranoside含量的方法。方法 采用SHIMADZU Shim-pack VP-ODS C18色谱柱(250 mm×4.6 mm,5 μm),乙腈-0.3%磷酸溶液为流动相,线性梯度洗脱,流速为1 mL·min-1;柱温为30℃,检测波长为350 nm。结果 Quercetin-3-O-(2'',6''-di-O-α-rhamnopyranosyl)-β-galactopyranoside和Kaempferol-3-O-[2-glucopyranosyl(1→3)rhamnopyranosyl-6-rhamnopyranosyl]-β-D-galactopyranoside分别在0.041 46~2.072 8 μg·mL-1r=0.999 9),0.088 95~4.447 5 μg·mL-1r=0.999 9)内呈良好的线性关系,平均加样回收率(n=6)分别为98.19%,98.85%;RSD分别为1.94%,1.81%。结论 建立的方法操作简单、专属性强,可用于同时测定细梗香草中2个专属黄酮苷类成分含量。
关键词:  细梗香草  高效液相色谱法  黄酮苷  含量测定
DOI:10.13748/j.cnki.issn1007-7693.2020.13.006
分类号:R917.101
基金项目:江西省重点研发计划项目(20161BBG70236);江西省食品药品监督管理局科技计划项目(2015YP08);国家药典委员会2015年国家药品标准提高项目(163)
Simultaneous Determination of Two Specific Flavonoid Glycosides in Lysimachia Capillipes Hemsl. by HPLC
ZHANG Kunyan1,2, HONG Ting1, WANG Dong3, JIAN Yongxue4, ZHAO Kai4, HUANG Jianli4, YANG Yisheng1
1.Jiangxi Provincial Institute for Drug Control, Jiangxi Provincial Engineering Research Center for Drug and Medical Device Quality, Nanchang 330029, China;2.Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China;3.Food Inspection and Testing Institute of Jiangxi Province, Jiangxi National Center for Quality Supervision and Inspection of Fruits, Vegetables, and Processed Food, Nanchang 330001, China;4.Jiangxi Ourshi Pharmaceutical Co., Ltd, Xinyu 338004, China
Abstract:
OBJECTIVE To establish an HPLC method for the simultaneous determination of Quercetin-3-O-(2'', 6''-di-O- α-rhamnopyranosyl)-β-galactopyranoside and Kaempferol-3-O-[2-glucopyranosyl(1→3)rhamnopyranosyl-6-rhamnopyranosyl]- β-D-galactopyranoside in Lysimachia capillipes Hemsl. METHODS The HPLC analysis was carried on SHIMADZU Shim- pack VP-ODS C18 column(250 mm×4.6 mm, 5 μm) with mobile phase consisted of acetonitrile-0.3% phosphoric acid aqueous solution (gradient elution) at the flow rate of 1 mL·min-1. The column temperature was set at 30℃, and the detection wavelength was set at 350 nm. RESULTS Quercetin-3-O-(2'',6''-di-O-α-rhamnopyranosyl)-β-galactopyranoside and Kaempferol-3-O-[2- glucopyranosyl(1→3)rhamnopyranosyl-6-rhamnopyranosyl]-β-D-galactopyranoside were showed good linear relationships within the ranges of 0.041 46-2.072 8 μg·mL-1(r=0.999 9) and 0.088 95-4.447 5 μg·mL-1(r=0.999 9). The average recoveries (n=6) were 98.19% and 98.85%, RSDS were 1.94% and 1.81%, respectively. CONCLUSION The established method is simple, specific, and suitable for simultaneous determination of two components of specific flavonoid glycosides in Lysimachia capillipes Hemsl.
Key words:  Lysimachia capillipes Hemsl  HPLC  flavonoid glycosides  component determination
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