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作 者:张任[1] 陈琴华[1,2] 朱军[2] 余飞[1,2]
机构地区:[1]湖北医药学院附属东风医院肾病内科,十堰442008 [2]湖北医药学院附属东风医院药物分析与筛选研究所,十堰442008
出 处:《医药导报》2015年第1期102-104,共3页Herald of Medicine
基 金:湖北省卫生厅青年科技人才项目(QJX2012-45);湖北省教育厅科研计划项目(D20132106)
摘 要:目的 建立气相色谱-质谱联用法测定蛇床子超临界二氧化碳(C02)流体提取物中蛇床子素的含量.方法 样品采用C02超临界流体萃取,萃取液用乙酸乙酯溶解,选择监测离子法测定蛇床子素的含量.色谱条件:DB-5 MS(30 m×0.32 mm,0.25 μm)石英毛细管色谱柱;柱流速2.0 mL·min^-1,柱温60℃保持2 min,以10℃·min^-1到280℃,保持6 min;进样口和接口温度为280 ℃.结果 蛇床子素在5~1 000μg·mL^-1线性关系良好,r=0.999 1,平均回收率为98.97%,检测限1.0 ng·mL^-1.结论 该方法稳定可靠,适用于蛇床子药材的质量控制.Objective To establish a method for content determination of osthole from Cnidium monnieri in supercritical fluid CO2(SFE-CO2) extract by gas chromatography-mass spectrometry (GC-MS). Methods The sample was extracted from Cnidium monnieri by SFE-CO2 and solved by acetic ether. The content of ostholei determined by GC-MS with selected ion monitor(GC-MS/SIM). Separation was performed on DB-5MS capillary column (30 m×0.32 mm,0.25 μm) at the flow rate of 2.0 mL · min^-1. The column temperature was started at 60℃ for 2 min, then increased to 280 ℃ at 10 ℃· min^-1 and maintained at 280 ℃ for 6 rain. The temperature of both interface and inlet was kept at 280 ℃. Results The linear range of osthole was within 5-1 000 μg · mL^-1 ( r = 0. 999 1 ). The mean extraction recovery was 98.97% and limit of detection was 1.0 ng · mL^-1. Conclusion The method is reliable and stable,which can be applied to quality control of Cndium monnieri.
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