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作 者:李承花[1] 刘婧慧[2] 徐珍霞[2] 赵文[2] 张晓琦[2,3] 张婷婷[2] 马志国[2,3]
机构地区:[1]暨南大学生命科学技术学院药物载体实验室,广州510632 [2]暨南大学药学院,广州510632 [3]暨南大学中药药效物质基础及创新药物研究广东省高校重点实验室,广州510632
出 处:《药物分析杂志》2010年第6期1003-1006,共4页Chinese Journal of Pharmaceutical Analysis
基 金:国家自然科学基金项目(No.30902001);暨南大学211项目
摘 要:目的:建立RP-HPLC同时测定管花肉苁蓉药材中松果菊苷、管花苷A、毛蕊花糖苷和异毛蕊花糖苷含量的方法。方法:采用Megres-C18(250mm×4.6mm,5μm)色谱柱,柱温30℃;流动相为甲醇(A)-0.1%甲酸(B),梯度洗脱(0min,30%A;30min,40%A;40min,45%A),流速1.0mL·min-1;检测波长330nm。结果:在上述色谱条件下,松果菊苷、管花苷A、毛蕊花糖苷和异毛蕊花糖苷获得良好分离;进样量分别在0.732~11.7μg(r=0.9991)、0.216~3.45μg(r=0.9995)、0.209~3.35μg(r=0.9991)、0.151~2.42μg(r=0.9993)范围内呈良好的线性关系;平均加样回收率(n=9)分别为101.8%,98.8%,101.1%,99.9%;精密度试验的RSD小于0.65%;重复性试验的RSD小于2.4%。结论:该方法简便、准确,重复性好,为管花肉苁蓉药材的质量控制提供可借鉴的分析方法。Objective:To simultaneous determine the contents of echinacoside,tubuloside A,acteoside and isoacteoside in rhizome of Cistanche tubulosa(Schrenk)Wight by RP-HPLC.Methods:An external standard method by RP-HPLC with Megres-C18(250 mm×4.6 mm,5 μm)as fixed phase at the temperature 30 ℃.The mobile phase consisted of methanol(A)-0.1% aqueous methanoic acid(B)with the gradient elution(0 min,30%A;30 min,40%A;40 min,45%A),the flow rate:1.0 mL·min-1.The Absorbance was monitored 330 nm.Results:Echinacoside,tubuloside A,acteoside and isoacteoside were well separated by this method.Linearities of echinacoside,tubuloside A,acteoside and isoacteoside were good in the ranges of 0.732-11.7 μg(r=0.9991),0.216-3.45 μg(r=0.9995),0.209-3.35 μg(r=0.9991),0.151-2.42 μg(r=0.9993),respectively.The average recoveries(n=9)of four phenylethanoid glycosides were 101.8%,98.8%,101.1%,99.9%,respectively.All of RSDs of precision(n=6)and repeatability(n=6)were less than 0.65% and 2.4%.Conclusion:The method is simple,accurate,reproducible,and can be used for quality control of Cistanche tubulosa(Schrenk)Wight.
分 类 号:R917[医药卫生—药物分析学]
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