摘要
目的:建立人参饮片的含量测定方法,并通过测定市售人参药材及饮片的总皂苷含量,进而探讨人参饮片的质量。方法:采用HPLC测定了5批人参药材及10批饮片中人参皂苷Rb1、Re、Rg1的含量。结果:人参药材与饮片总皂苷含量差异较大,且炮制后人参饮片中人参皂苷含量降低。结论:人参药材炮制后其质量存在明显变化,亟需制定统一标准进行质量控制。
To establish a content determination method for the decoction pieces of ginseng radix et Rhizoma and investi- gate the quality of the slices by measuring the content of ginsenoside in commercially available crude materials and the decoction pieces. Methods: An HPLC method was used to determine the content of ginsenoside RbI, Re and Rgl in the crude materials and decoction pieces of ginseng radix et Rhizoma. Results: Significant difference in ginsenoside content between the medicinal materials and decoction pieces was found, and saponin content in the slices was decreased. Conclusion:The quality of the slices of g/nseng radix et Rhizoma is changed significantly, and it is urgent to develop a agreed standard for the quality control of ginseng radix et Rhizoma during the processing.
出处
《中国药师》
CAS
2014年第5期794-797,共4页
China Pharmacist
基金
国家药品标准提高暨2015版药典科研任务
关键词
人参药材
人参饮片
炮制
总皂苷
含量测定
Ginseng radix et Rhizoma
Ginseng Pieces
Processing
Total saponins
Content determination