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机构地区:[1]重庆三峡中心医院药剂科,重庆市404000 [2]重庆市中药研究院,重庆市400065 [3]重庆医药高等专科学校,重庆市401331
出 处:《中国药房》2011年第47期4473-4475,共3页China Pharmacy
摘 要:目的:建立妇血宁颗粒的质量标准。方法:采用薄层色谱(TLC)法对方中三七、断血流进行定性鉴别;采用高效液相色谱法测定三七皂苷R1、人参皂苷Rb1、人参皂苷Rg1的含量。结果:TLC斑点清晰,分离度好,阴性对照无干扰;三七皂苷R1、人参皂苷Rb1、人参皂苷Rg1的进样量分别在0.44~4.40(r=0.9998)、0.82~8.20(r=0.9999)、0.74~7.40(r=0.9997)μg范围内与各自峰面积积分值呈良好线性关系;平均回收率分别为98.21%、98.52%、98.76%,RSD分别为0.81%、0.77%、0.91%(n均为6)。结论:所建标准可用于该制剂的质量控制。OBJECTIVE: To establish the quality standards of Fuxuening granules. METHODS: Identification of Panax notoginseng and Clinopodium Herb was carded out by TLC; HPLC method was adopted for the content determination of notoginsenoside R1, ginsenoside Rb1 and ginsenoside RgL in Fuxuening granules. RESULTS: TLC sports developed were fairy clear and well-separated with no interference from negative control. The linear ranges were 0.44~4.40μg (r=0.999 8) for notoginsenoside R1,0.82~8.20μg(r=0.999 9)for ginsenoside Rb1,0.74~7.40μg(r=0.999 7)for ginsenoside Rgrespectively. The averages recovery were 98.21% (RSD:0.81% ,n=6), 98.52% (RSD:0.77%, n=6), 98.76% (RSD=0.91%, n=6). CONCLUSION:Established standard is suitable for quality control of Fuxuening granules.
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