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作 者:崔兰冲[1] 沈晓君[1] 蔡广知[1] 贡济宇[1]
机构地区:[1]长春中医药大学国家中医药管理局中药分析三级实验室,长春130117
出 处:《中国实验方剂学杂志》2013年第10期112-114,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:吉林省教育厅"十一五"科学技术研究项目(吉教科合字[2008]第89号)
摘 要:目的:建立色谱-原子荧光光谱联用技术分离测定不同形态砷的方法。方法:色谱-原子荧光光谱联用技术对砷进行测定。色谱及光谱条件如下,阴离子分离柱PRP-X100(4.1 mm×250 mm,10μm),流动相15 mmoL.L-1(NH4)2HPO4(pH6.0),流速1 mL.min-1,柱温25℃。As空心阴极灯,灯电流/辅阴极灯电流:100/46 mA。结果:砷含量在0.002~0.01μg线性关系良好,平均回收率为97.35%(n=6),RSD 1.5%。结论:方法灵敏,准确,重复性好,是分离测试不同形态砷的有效方法。Objective: To establish the method of chromatography-AFS for separating and determining As from different existing forms in Bupleurum chinense. Method: Chromatography-AFS was used to determine the content of As. The conditions of chromatography and spectrum were as follows: negative ion column of PRP-X100 (4.1 mm×250 mm, 10 μm) was used, mobile phase was the solution of 15 mmoLL-1 (NH4)2HPO4 (pH 6.0). The flow rate was 1 mLmin-1; column temperature was set at 25 ℃; element lamp was hollow cathode lamp of As, lamp current/auxiliary cathode lamp current was 100/46 mA. Result: The standard curve was linear in the range of 0.002-0.01 μg. The average recovery was 97.35% with RSD 1.5% (n=6). Conclusion: The method is sensitive, accurate and reproducible. It can be used to determine the content of As in different existing forms.
关 键 词:北柴胡 色谱-原子荧光光谱联用 砷 含量测定
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