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作 者:孙晓东[1,2] 王文辉[1,2] 杨俊[1,2] 朱艳琴[1,2] 王齐[1,2]
机构地区:[1]昆明理工大学分析测试研究中心,昆明市学府路253号650093 [2]云南省分析测试中心,昆明市学府路253号650093
出 处:《光谱实验室》2010年第4期1282-1285,共4页Chinese Journal of Spectroscopy Laboratory
摘 要:建立了反相高效液相色谱法同时测定银黄含片中的黄芩苷、绿原酸和芦丁。采用HypersilODSC18柱(200mm×4.6mm,粒径5μm),流动相A:甲醇-水-乙酸(10∶88∶2)和流动相B:甲醇-水-乙酸(88∶10∶2),梯度洗脱程序0min(A∶B/97∶3)-10min(A∶B/73∶27)-25min(A∶B/20∶80)-36min(A∶B/20∶80);流速1.0mL/min;检测波长为327nm和280nm;柱温25℃。黄芩苷线性范围为0.051—0.512μg/mL,r=0.9990,样品的平均加标回收率为98.23%,(RSD为2.13%);绿原酸线性范围为0.059—0.592μg/mL,r=0.9996,样品的平均加标回收率为97.61%,(RSD为2.13%);芦丁线性范围为0.087—0.868μg/mL,r=0.999,样品的平均加标回收率为98.56%,(RSD为1.13%),该方法专属性强,结果稳定,重现性好,能有效地控制药品的主成分含量,具有较强的实用价值。A method for simultaneous determination of baicalin,chlorogenic acid and rutin in the yin huang buccal tablets was developed.A hypersil ODS C18(4.6mm×200mm,5μm) column was used.A mixture of methanol-water-acetic acid(10:88:2)was used as mobile phase A and the mixture of methanol-water-acetic acid(88:10:2) as mobile phase B.Phase A-phase B in gradient elution:0 min (97:3)-10min(73:27)-25min(20:80)-36min(20:80) at a flow rate of 1.0mL/min.The detection wavelength was set at 327 nm and 280 nm and the column temperature was 25℃.The calibration curve was linear in the range of 0.051—0.512μg/mL for baicalin(r=0.9990),average recovery was 98.23% and RSD was 2.13% (n=6).The calibration curve was linear in a range of 0.059—0.592μg/mL for chlorogenic acid(r=0.9996),average recovery was 97.61% and RSD was 2.13%(n=6).The calibration curve was linear in a range of 0.087—0.868μg/mL for rutin(r=0.9992),average recovery was 98.56% and RSD was 1.13%(n=6).The method is sensitive,reproducible,and suitable for the quality control of the yin huang buccal tablets.
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