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作 者:汤道权[1,2,3] 张尊建[1,2] 高媛媛[3] 魏雅芹[3] 韩琳[3]
机构地区:[1]药物质量与安全预警教育部重点实验室,江苏南京210009 [2]中国药科大学分析测试中心,江苏南京210009 [3]徐州医学院药物分析教研室,江苏徐州221004
出 处:《中草药》2009年第1期56-60,共5页Chinese Traditional and Herbal Drugs
基 金:江苏省高校自然科学基金资助项目(07KJD360225)
摘 要:目的建立固相萃取-反相高效液相色谱法同时测定银杏叶提取物中芦丁、槲皮素、山柰酚和异鼠李素的方法。方法采用Waters Sep-Park-C18固相萃取小柱对银杏叶提取物样品进行处理,流动相:甲醇-0.1%甲酸水溶液,线性梯度洗脱;检测波长:360nm;柱温:40℃;进样量:20μL;体积流量:1.0mL/min。结果芦丁、槲皮素、山柰酚、异鼠李素的定量限分别为20、6、5、5mg/mL,芦丁、槲皮素、山柰酚、异鼠李素分别在14~198、15~205、3~40、3~41mg/L时与峰面积线性关系良好,回收率为93.7%~104.7%,日内及日间精密度的RSD分别小于2%、3%。结论方法简单、准确,为银杏叶提取物中黄酮类成分的质量控制提供了依据。Objective To determine four flavonol components as markers, rutin, quercetin, kaempferol, and isorhamnetin for quality control of extract of Ginkgo biloba (EGb) by a validated high performance liquid chromatographic (HPLC) method with solid phase extraction. Methods The four flavonols of EGb were extracted with Waters Sep-Park-C18 solid-phase extraction column. Separation was achieved using a Kromasil C18 column (250 mm×4.6 mm, 5 μm ) at 40 ℃ with a step linear gradient using methanol : 0.1% formic acid at a flow rate of 1.0 mL/min, wavelength was 360 nm, sample amount was 20μL. Results The limits of quantitation for rutin, quercetin, kaempferol, and isorhamnetin were 20, 6, 5, and 5 mg/mL, respectively. This method was linear over concentration ranges of 14--198, 15--205, 3--40 and 3--41 mg/L for rutin, quercetin, kaempferol, and isorhamnetin, respectively. The solid phase extraction recoveries for rutin, quercetin, kaempferol, and isorhamnetin were 93.7%-104.7%. The precision of intra-day and inter-day were less than 2 % and 3% for all compounds, repectively. Conclusion The validated method is simple, accurate, and able to provide the basis for the quality control of flavonols in EGb.
关 键 词:银杏叶提取物(EGb) 固相萃取 HPLC
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