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作 者:梁丽娟[1] 赵奎君[1] 屠鹏飞[2] 姜勇[2]
机构地区:[1]首都医科大学附属北京友谊医院,北京市100050 [2]北京大学医学部药学院,北京市100083
出 处:《中国药房》2010年第15期1385-1387,共3页China Pharmacy
基 金:国家重点基础研究发展计划973计划课题(2006CB504707)
摘 要:目的:建立以高效液相色谱法同时测定11个产地黄芪中毛蕊异黄酮葡萄糖苷、芒柄花苷、毛蕊异黄酮和芒柄花素4种黄酮类成分含量的方法,从有效成分含量探讨药材道地性内在因素。方法:色谱柱为Zorbax Eclipse XDB-C1(8250mm×4.6mm,5μm),流动相为乙腈-0.2%甲酸水溶液(梯度洗脱),检测波长为280nm。结果:毛蕊异黄酮葡萄糖苷、芒柄花苷、毛蕊异黄酮和芒柄花素的检测浓度分别在0.0051~0.510、0.0050~0.300、0.0049~0.294、0.0046~0.276mg·mL-1范围内与各自峰面积积分值呈良好的线性关系(r均为0.9999)。内蒙古、山西等4个产地的黄芪中毛蕊异黄酮苷和芒柄花苷的含量较高;河北安国、赤城和甘肃定西产黄芪中毛蕊异黄酮和芒柄花素含量较高。结论:本方法简便、快速、准确,试验结果与黄芪本草考证、道地沿革的文献基本相符。OBJECTIVE:To develop an HPLC method for simultaneous determination of calycosin-7-O-β-D-glycoside,ono-nin,calycosin and formononetin in Radix Astragali from eleven different habitats and to explore the internal factors of geoherbalism based on aspect of contents of active constituents. METHODS:The sample was separated on Zorbax Eclipse XDB-C18(250 mm×4.6 mm,5 μm)column. The mobile phase consisted of acetonitrile-0.2% formic acid solution (gradient elution). The UV detection wavelength was set at 280 nm. RESULTS:The linear ranges of calycosin-7-O-β-D-glycoside,ononin,calycosin and formononetin were 0.005 1~0.510 mg·mL-1,0.005 0~0.300 mg·mL-1,0.004 9~0.294 mg·mL-1,0.004 6~0.276 mg·mL-1,respectively(r=0.999 9).Calycosin-7-O-β-D-glycoside and ononin took up a big proportion in Radix Astragali from Inner Mongolia and Shanxi; calycosin and formononetin took up a big proportion in Radix Astragali from Anguo,Chicheng of Hebei province and Dingxi of Gansu province. CONCLUSION:The method is simple,rapid and accurate. Results of study are in line with textual research on Radix Astragali.
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