参芪强身口服液质量标准的研究  

The Standard of Quality Control for Shen Qi Qiang Shen Oral Liquid

作　　者：何夏秋[1] 高树棣[1] 贺建华[1] 李连达[1] 赵素民 李珍 

机构地区：[1]中国中医研究院西苑医院基础室,宁夏回族自治区中医研究院

出　　处：《中药新药与临床药理》1995年第4期48-51,共4页Traditional Chinese Drug Research and Clinical Pharmacology

摘　　要：报导了参芪强身口服液中人参、黄芪及大黄的薄层鉴别方法，并用薄层扫描法测定了人参皂甙Ｒｇ１的含量范围在０．００７０５３～０．００８１４５％之间．平均回收率为９８．８１％，ＣＶ％为２．１３。该法灵敏度高，重现性好。Radix Ginseng, Radix Astragali and Radix ct Rhizoma Rhei in.Shen Qi Qiang Shen oral liquid were identified by TLC and the conlent of ginscnoside Rg1 was also deter -mined. The results showed that the content ofginsenoside Rg, was 98.81%and the coefficient Vrariation was 2. 13 %. This method is found to be hightly sensitive and reproducible, andmay be used as a standard for the quality control of this compound preparation.

关 键 词：参芪强身口服液 人参皂甙 黄芪 大黄素 

分 类 号：R286.0[医药卫生—中药学]