中国药品标准2024,Vol.25Issue(4) :392-397.DOI:10.19778/j.chp.2024.04.012

UPLC法同时测定紫龙金片中野黄芩苷等8种成分的含量

Simultaneous determination of eight components including scutellarin in Zilongjin tablets by UPLC

黄丽
中国药品标准2024,Vol.25Issue(4) :392-397.DOI:10.19778/j.chp.2024.04.012

UPLC法同时测定紫龙金片中野黄芩苷等8种成分的含量

Simultaneous determination of eight components including scutellarin in Zilongjin tablets by UPLC

黄丽1
扫码查看

作者信息

  • 1. 厦门市食品药品质量检验研究院,福建厦门 361012
  • 折叠

摘要

目的:建立同时测定紫龙金片中新绿原酸、绿原酸、咖啡酸、隐绿原酸、阿魏酸、野黄芩苷、丹酚酸B、芹菜素含量的超高效液相色谱法.方法:采用Waters Acquity UPLC HSS T3(2.1 mm × 100 mm,1.8 µm)色谱柱,以乙腈-0.1%磷酸进行梯度洗脱,进样量1 μL,柱温为30 ℃,流速为0.3 mL·min-1,检测波长为323 nm.结果:8种成分在各自质量浓度范围内线性关系良好(r>0.999 0),平均加样回收率94.1%~101.6%,RSD%0.70%~1.93%.测定4批样品,不同批次样品除新绿原酸、绿原酸、隐绿原酸含量略有差异,其余成分含量基本一致.结论:本法简便、高效、准确,可综合全面地评价本品的内在质量,更好地为紫龙金片的质量评价提供参考.

Abstract

Objective:To establish a UPLC method for the simultaneous determination of neochlorogenic acid,chlorogenic acid,caffeic acid,cryptochlorogenic acid,ferulic acid,scutellarin,salvianolic acid B,and apigenin in Zilongjin tablets.Methods:Waters Acquity UPLC HSS T3 column(2.1 mm × 100 mm,1.8 µm)was used.Gradient elution was performed with acetonitrile and 0.1%phosphoric acid.The injection volume was 1 µL,the column temperature was set at 30 ℃ the flow rate was 0.3 mL·min-1,and detection was carried out at 323 nm.Results:The linear relationship between the 8 components within their respective mass concentration ranges was good(r>0.999 0),with average recovery of 94.1%to 101.6%and RSD%of 0.70%to 1.93%.Four batches of sam-ples were tested,and the content of the other components in different batches was basically same,except slight differ-ences in the content of neochlorogenic acid,chlorogenic acid,and cryptochlorogenic acid.Conclusion:This method is simple,efficient,and accurate,and can comprehensively evaluate the intrinsic quality of this product,which pro-vides a better reference for the quality evaluation of Zilongjin tablets.

关键词

紫龙金片/野黄芩苷/丹酚酸B/UPLC/含量测定/质量评价

Key words

Zilongjin tablets/scutellarin/salvianolic acid B/UPLC/content determination/quality evaluation

引用本文复制引用

出版年

2024
中国药品标准
国家药典委员会

中国药品标准

影响因子:0.372
ISSN:1009-3656
段落导航相关论文