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引用本文:李嘉,张颖,姜平川,张赟赟.广西不同产地壮药玉叶金花中Mussaendoside G的含量测定[J].中国现代应用药学,2014,31(12):1478-1480.
LI JIA,ZHANG Ying,JIANG Pingchuan,ZHANG Yunyun.Determination of Mussaendoside G in Mussaenda Pubescens in Different Areas of Guangxi Province by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2014,31(12):1478-1480.
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广西不同产地壮药玉叶金花中Mussaendoside G的含量测定
李嘉1,2, 张颖1,2, 姜平川1,2, 张赟赟1,2
1.广西壮族自治区中药质量标准研究重点实验室,南宁 530022;2.广西壮族自治区中医药研究院化学所,南宁 530022
摘要:
目的 建立高效液相色谱法测定玉叶金花中mussaendoside G的含量。方法 色谱柱为Techmate C18(4.6 mm× 250 mm,5 μm),流动相:乙腈-水(38∶62),检测波长:265 nm,流速:1.0 mL·min-1。结果 mussaendoside G在0.06~ 0.60 mg·mL-1(r=0.999 9)内线性关系良好,平均回收率为99.34%,RSD为2.32%。不同产地玉叶金花中mussaendoside G的含量相差较大。结论 此方法简便、快捷、准确,可用于玉叶金花药材的质量控制。
关键词:  mussaendoside G  玉叶金花  含量测定  高效液相色谱法
DOI:
分类号:
基金项目:广西壮族自治区科技厅项目(桂科能12239004-2)
Determination of Mussaendoside G in Mussaenda Pubescens in Different Areas of Guangxi Province by HPLC
LI JIA1,2, ZHANG Ying1,2, JIANG Pingchuan1,2, ZHANG Yunyun1,2
1.Guangxi Key Laboratory of the Quality Standard of Traditional Chinese Medicine, Nanning 530022, China;2.Department of Chemistry, Guangxi Institute of Chinese Medicine & Pharmaceutical Science, Nanning 530022, China
Abstract:
OBJECTIVE To establish an HPLC method for the simultaneous determination of mussaendoside G in Mussaenda pubescens in different areas of Guangxi province. METHODS Mussaendoside G was separated on Techmate C18 (4.6 mm×250 mm, 5 μm) column and detected at 265 nm. The mobile phase was acetonitrile-water(38∶62). The flow rate was 1.0 mL·min-1. RESULTS Mussaendoside G was 1inear within the range of 0.06-0.60 mg·mL-1(r=0.999 9). The average recovery was 99.34%(RSD=2.32%). The contents of mussaendoside G in different areas were different. CONCLUSION The method is simple, rapid, and it can be used for the quality control of Mussaenda pubescens.
Key words:  mussaendoside G  Mussaenda pubescens  content determination  HPLC
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