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郁福来胶囊质量标准研究

倪玉佳 瞿发林

中国药业2017,Vol.26Issue(4):16-19,4.
中国药业2017,Vol.26Issue(4):16-19,4.DOI:10.3969/j.issn.1006-4931.2017.04.004

郁福来胶囊质量标准研究

Quality Control Standard of Yufulai Capsules

倪玉佳 1瞿发林1

作者信息

  • 1. 中国人民解放军第102医院制剂中心,江苏常州 213003
  • 折叠

摘要

Abstract

Objective To study the quality control standard of Yufulai Capsules. Methods Herba hyperici perforati and hyperoside in Yufulai Capsules were identified by thin-layer chromatogram(TLC). An HPLC method was used for the determination of hyperoside in Yufulai Capsules. Results Herba hyperici perforati and hyperoside were separated from other components well. The linear ranges of hyperoside was 0. 173-1. 73 μg,r=0. 9999(n=6). The average recovery of hyperoside was 99. 65%,RSD=1. 00% (n=6). Conclusion The method is simple,sensitive and reliable,which can be applied in the quality control of Yufulai capsules.

关键词

郁福来胶囊/贯叶金丝桃/金丝桃苷/质量标准

Key words

Yufulai Capsules/herba hyperici perforati/hyperoside/quality standard

分类

医药卫生

引用本文复制引用

倪玉佳,瞿发林..郁福来胶囊质量标准研究[J].中国药业,2017,26(4):16-19,4.

基金项目

军队医疗机构制剂标准提高科研专项课题(13ZJZ16-3). (13ZJZ16-3)

中国药业

OACSTPCD

1006-4931

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