畜牧与饲料科学 ›› 2018, Vol. 39 ›› Issue (5): 1-1.doi: 10.12160/j.issn.1672-5190.2018.05.001

• 基础科学 •    下一篇

苦玄参提取物中苦玄参苷ⅠA质量控制方法的建立

刘妍璨[1];王秋华[1];黄宏业[2];段群棚[3];林昌华[4];蒋家霞[4];张宁[5];郭旋[5];胡庭俊[1];何颖[3]   

  1. [1]广西大学动物科学技术学院,广西南宁530005;[2]广西北斗星动物保健品有限公司,广西南宁530003;[3]广西兽医生物技术重点实验室,广西南宁530001;[4]广西农垦永新畜牧集团新兴有限公司,广西柳州545112;[5]广西农垦永新畜牧集团金光有限公司,广西南宁530022
  • 出版日期:2018-05-20 发布日期:2018-05-20
  • 通讯作者: 刘妍璨
  • 作者简介:刘妍璨(1992-),女,硕士研究生,主要研究方向为中兽药制剂开发。;通讯作者:胡庭俊(1965-),男,教授,博士生导师,主要研究方向为兽医药理与毒理学。;通讯作者:何颖(1979-),女,副研究员,主要研究方向为动物药学与动物分子病毒学。
  • 基金资助:
    广西柳州市柳江区科学研究与技术开发计划项目(201709); 广西南宁市西乡塘区科学研究与技术开发计划项目(201710317); 广西基本科研业务费专项(桂科专项16-2); 南宁市科学研究与技术开发计划项目(20155181)

Establishment of Quality Control Method for PicfeltarraeninⅠA in Picria fel-terrae Extracts

LIU Yan-can1,WANG Qiu-hua1, HUANG Hong-ye2, DUAN Qun-peng3, LING Chang-hua4, JIANG Jia-xia4, ZHANG Ning5, GUO Xuan5, HU Ting-jun1, HE Ying3 (1.College of Animal Science and Technology,Guangxi University,Nanning 530005,China;2. Guangxi Beidouxing Animal Health Products Co., Ltd., Nanning 530003,China; 3.Guangxi Key Laboratory of Veterinary Biotechnology, Nanning 530001, China;4.Xinxing Co.,Ltd. of Yongxin Animal Husbandry Group of Guangxi State Farm,Liuzhou 545112,China;5.Jinguang Co., Ltd. of Yongxin Animal Husbandry Group of Guangxi State Farm, Nanning 530022, China)   

  • Online:2018-05-20 Published:2018-05-20

摘要: [目的]建立苦玄参提取物中苦玄参苷ⅠA的鉴别和含量测定方法。[方法]采用薄层色谱法对苦玄参苷进行定性鉴别;采用高效液相色谱法测定提取物中苦玄参苷ⅠA的含量,色谱条件为:Waters Symmetry C18(4.6×250 mm,5μm)色谱柱,流动相为乙腈—水(35∶65),流速1.0 m L/min,检测波长264nm,柱温35℃,进样量20μL。[结果 ]苦玄参苷ⅠA的薄层色谱鉴别方法专属性强;苦玄参苷ⅠA在20.06~104.10μg/m L的质量浓度范围内线性关系良好(R2=0.9992),平均加样回收率为99.90%,RSD=0.53%。[结论]建立的方法专属性强,定量准确性高,适用于苦玄参提取物的质量控制。

Abstract: [Objective]To establish an identification and content determination method for picfeltarraeninⅠA in Picria fel-terrae extracts. [Methods]The qualitative identification of picfeltarraenin ⅠA was carried out with thin layer chromatography(TLC)method; high performance liquid chromatography(HPLC) method was used to determine the content of picfeltarraenin ⅠA in Picria fel-terrae extracts, and the chromatography conditions were as followed: the chromatographic column was Waters Symmetry C18(4.6 ×250 mm, 5 μm), the mobile phase was acetonitrile-water(35 ∶65), the velocity was 1.0 m L/min, the detecting wavelength was 264 nm, the column temperature was 35 ℃, and the injection volume was 20 μL. [Results]The TLC method showed high specialization for identification of picfeltarraenin ⅠA . A good linear relationship was observed in the mass concentration range of 20.06-104.10 μg/m L(R2=0.9992);the average recovery rate was 99.90%, and the RSD was 0.53 %.[Conclusion]The established method in this study has good specialization in qualitative analysis and has high accuracy in quantitative analysis and can be used in quality control of picfeltarraeninⅠA in Picria fel-terrae extracts.

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