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机构地区:[1]辽宁省大连市儿童医院药剂科,大连116011 [2]辽宁省大连市皮肤病医院,大连116011
出 处:《海峡药学》2007年第9期31-33,共3页Strait Pharmaceutical Journal
摘 要:目的建立小儿肺炎舍剂中黄芩苷的RP—HPLC含量测定方法,为制定质量标准提供依据。方法采用Symmetry C18柱(3.9×150mm,5μm);流动相为甲醇-水-磷酸-三乙胺(50:40:0.2:2);柱温:38℃;流速1mL·min^-1;检测波长277nm。结果黄芩苷在进样量为0.020~1.000μg范围内线性关系良好(r=0.9999),平均加样回收率为99.89%,RSD=1.02%。结论所建立的方法灵敏度高,可靠性好,操作方便,可作为肺炎合剂的质量控制方法。OBJECTIVE To establish a determination method of baicalin in the children's pneumonia mixture by RP-HPLC,and to set up its quality control standard. METHODS A Symmetry C18 column was used with methanol-water-phosphoric acid-triethylamine ( 50: 40: 0. 2: 2 drops) as mobile phase, column temperature was at 38 ℃. The flow rate was 1mL·min^-1. The content was detected at the wavelength of 277nm. RESULTS The qualificationmethod of the baicalin had the linear range of 0. 020 ~ 1. 000μg( r = 0. 9999). The average recovery was 99.89% with RSD of 1.02%. CONCLUSION The method for quantification was sensitive reliable and convenient for quality control of children's pneumonia mixture.
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