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作 者:程丽媛[1] 梁勇 罗轩[1] 刘旭[1] 杨华[1] 王立升[1]
机构地区:[1]广西大学化学化工学院,广西南宁530004 [2]南宁骄阳医药科技有限公司,广西南宁530003
出 处:《广西大学学报(自然科学版)》2016年第6期2053-2059,共7页Journal of Guangxi University(Natural Science Edition)
基 金:广西自然科学基金重点项目(2010GXNSFD013040);广西科技攻关项目(桂科攻11107010-3-5)
摘 要:建立了一种可以对菥蓂药材中5,7-二羟基-4'-O-(6″-O-β-D-葡萄糖)-β-D-葡萄糖黄酮、异肥皂草苷、异荭草苷、牡荆苷、异牡荆苷、木犀草苷和大波斯菊苷的含量进行同时测定的RP-HPLC法。色谱条件:色谱柱为Agilent C18柱(4.6×150 mm,3.5μm);流动相为乙腈-0.4%冰醋酸水溶液,梯度洗脱;流速1.0 m L/min;检测波长273 nm;柱温35℃。结果表明,在上述色谱条件下,5,7-二羟基-4'-O-(6″-O-β-D-葡萄糖)-β-D-葡萄糖黄酮、异肥皂草苷、异荭草苷、牡荆苷、异牡荆苷、木犀草苷和大波斯菊苷的质量浓度分别在5.67-56.7μg/m L(r=0.999 7),10.92-109.2μg/m L(r=0.999 4),5.76-57.6μg/m L(r=0.9998),4.92-49.2μg/m L(r=0.999 8),13.95-139.5μg/m L(r=0.999 9),5.25-52.5μg/m L(r=0.999 8),5.22-52.2μg/m L(r=0.999 7)范围内与色谱峰的峰面积呈现良好的线性关系,平均加样回收率均在97%-101%,RSD均小于2.7%。该分析方法简便、快速、准确且重现性好,为有效地监控菥蓂药材的质量提供了可靠方法。A RP-HPLC method for simultaneous determination of 5,7-dihydroxy-flavone-4'-( 6″-O-β-D-glucopyranoside)-O-β-D-glucopyranoside,isosaponarin,isoorientin,vitexin,isovitexin,luteolin-7-O-β-D-glucoside and apigenin-7-O-β-D-glucoside in Thlaspi arvense L was established. Theseparation was performed on an Agilent C18column( 4. 6×150 mm,3. 5 μm) with a gradient elution composed of acetonitrile and 0. 4% acetic acid aqueous solution. The column temperature was set at35 ℃,and the flow rate was 1. 0 m L / min. The detective wavelength was set at 273 nm. The results indicated that the linear range was 5. 67 - 56. 7 μg / m L( r = 0. 999 7),10. 92 - 109. 2 μg / m L( r =0. 999 4),5. 76 - 57. 6 μg / m L( r = 0. 999 8),4. 92 - 49. 2 μg / m L( r = 0. 999 8),13. 95 -139. 5 μg / m L( r = 0. 999 9),5. 25 - 52. 5 μg / m L( r = 0. 999 8),and 5. 22 - 52. 2 μg / m L( r =0. 999 7),respectively( n = 6). The average recoveries( n = 3) of seven flavonoids were 97% -101%,and the RSDs were less than 2. 7%. The method is simple,rapid,accurate and reproducible,and can be effectively used for the quality control of Thlaspi arvense L.
分 类 号:R917[医药卫生—药物分析学]
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