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机构地区:[1]武警浙江省总队医院药剂科,浙江嘉兴314000
出 处:《中国医院用药评价与分析》2014年第1期55-57,共3页Evaluation and Analysis of Drug-use in Hospitals of China
摘 要:目的:应用高效液相色谱-蒸发光散射检测器(HPLC—ELSD)法测定黄连清胃丸中栀子苷、知母皂苷AⅢ和知母皂苷BⅡ的含量。方法:采用C18色谱柱(4.6mmX250mm,5μm);流速为0.9ml/min;乙腈-水(30:70)为流动相;ELSD漂移管温度为90℃;载气(M)流速为2.9SLPM/min。结果:栀子苷、知母皂苷AⅢ和知母皂苷BⅡ进样量分别在0.0618—1.2360μg(r=0.9992)、0.0476~0.9520μg(r=0.9997)和0.1842~3.6840μg(r=0.9993)时进样量的自然对数值与峰面积的自然对数值呈良好的线性关系,平均加样回收率分别为97.67%、98.18%和98.36%,RSD分别为1.09%、1.01%和0.98%(n=6)。结论:本方法测定结果准确、灵敏、重复性好。OBJECTIVE: To develop HPLC-ELSD method for determination of the contents of Geniposide, Timosaponin AⅢ and Timosaponin B Ⅱ in Huanglian Qingwei Pills. METHODS: C18 column (4. 6 mm ×250 mm, 5 μm) was used as the chromatographic column with mobile phase consisting of Acetonitrile-Water (30: 70) at flow rate of 0. 9 ml/min ; the temperature of drift tube was set at 90 ℃ and the flow rate of the cartier gas ( N2 ) was set at 2. 9 SLPM/min. RESULTS: The linear ranges of Geniposide, Timosaponin Am, Timosaponin B II were 0. 061 8-1. 236 0 μg (r =0. 999 2), 0. 047 6-0. 952 0 μg (r =0. 999 7) and0. 184 2-3. 684 0 μg (r =0. 999 3), respectively with average recovery rates of 97.67% (RSD = 1.09% ), 98.18% (RSD = 1.01% ) and 98.3% (RSD =0. 98% ), respectively. CONCLUSION: The; established method is accurate in determination results, sensitive and reproducible.
关 键 词:黄连清胃丸 栀子苷 知母皂苷AⅢ 知母皂苷BⅡ 高效液相色谱一蒸发光散射检测器法
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