摘要
目的:建立苦参总碱中三氯甲烷残留的检测方法。方法:采用气相色谱顶空进样法,聚乙二醇(DB-WAX)毛细管柱,FID检测器,柱温采用程序升温,初始温度为60℃,保持6 min,然后以15℃.min-1升温速率升至180℃,保持5 min。结果:各个峰的分离效果好,三氯甲烷浓度在12.4~1236.6μg.mL-1的范围内呈良好的线性关系(r=0.9940),平均回收率为94.5%。结论:本方法结果准确、灵敏度高、重复性好,可以作为苦参总碱中三氯甲烷残留的检测方法。
Objective:To establish a method to determine the residual chloroform in matrine.Methods:Using DB-WAX capillary column,FID detector and program temperature.The initial temperature was kept at 60 ℃ for 6 minutes,then the temperature was raised to 180 ℃ at the rate of 15 ℃·min-1 and kept for 5 minutes.Results:All the peaks were completely separated,the calibration curve showed a good linearity with the range of 12.4-1236.6 μg·mL-1(r=0.9940).The average recovery was 94.5%.Conclusion:The method is accurate,sensitive and repetitive to determine residual chloroform in matrine.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2011年第9期1824-1826,共3页
Chinese Journal of Pharmaceutical Analysis
基金
宁夏十一五科技攻关项目
宁科技字[2006]74号