摘要
目的:建立银杏叶提取物中总银杏酸HPLC限量检测方法。方法:银杏叶提取物以甲醇直接溶解,制备供试品溶液;HPLC条件:以十八烷基硅烷键合硅胶为填充剂,0.1%三氟乙酸乙腈为流动相A,0.1%三氟乙酸水为流动相B,梯度洗脱(0~30 min,75%A→90%A;30~35 min,90%A),流速1 m L·min-1,检测波长310 nm。结果:白果新酸的线性关系良好,平均回收率(n=9)为93.8%。6个厂家10批银杏叶提取物依法进行测定,结果显示:不同厂家提取物总银杏酸含量存在较大差异。结论:该法经方法学验证,可用于银杏叶提取物中总银杏酸的限量检测。
Objective: To establish a method for the limit determination of total ginkgolic acid in Ginkgo biloba ex- tract by HPLC. Methods: Ginkgo biloba extract C18 column with 0. 1% trifluoroacetic acid in ac was dissolved with methanol. The determination was performed on etonitrile as the mobile phase A and 0. 1% trifluoroacetic acid in water as the mobile phase B with gradient elution mode (0-30 min, 75% A→90% A; 30-35 min, 90% A), at a flow rate of 1 mL · min-1. The detection wavelength was 310 nm. Results: There was a good linear relationship with ginkgoneolic acid ,and the average recovery( n = 9 )was 93.8%. Ten batches of Ginkgo biloba extract from six manu- facturers were determined. Extracts from different manufacturers showed significant differenes of content of total ginkgo acid. Conclusion: Through the validation of mothodology, this method can be used as the limit determination of ginkgolic acid.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2015年第11期2041-2044,共4页
Chinese Journal of Pharmaceutical Analysis
基金
国家药品标准提高暨2015年版药典科研任务