分散液液微萃取-反萃取-接受相固化-高效液相色谱法测定减肥茶中的西布曲明

建立了分散液液微萃取-反萃取-接受相固化与高效液相色谱联用测定减肥茶中西布曲明的方法。优化的条件为:400"L石油醚为萃取剂、120"L甲醇为分散剂、14"L 0.2 mol/L HCl溶液和1"L甲醇的混合溶液为接受相,萃取2 min。在优化条件下西布曲明的富集因子可达130倍。方法的线性范围为0.6~200"g/L,检测出限为0.2"g/L,定量限为0.6"g/L。样品加标回收率介于91.9%~108.4%,日间相对标准偏差小于14%。...

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Published in分析化学 Vol. 41; no. 9; pp. 1444 - 1448
Main Author 石慧 夏丹 邓晓庆 谭月明 苏孝礼 谢青季 马铭
Format Journal Article
LanguageChinese
Published 化学生物学及中药分析教育部重点实验室,湖南师范大学,长沙410081 2013
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Summary:建立了分散液液微萃取-反萃取-接受相固化与高效液相色谱联用测定减肥茶中西布曲明的方法。优化的条件为:400"L石油醚为萃取剂、120"L甲醇为分散剂、14"L 0.2 mol/L HCl溶液和1"L甲醇的混合溶液为接受相,萃取2 min。在优化条件下西布曲明的富集因子可达130倍。方法的线性范围为0.6~200"g/L,检测出限为0.2"g/L,定量限为0.6"g/L。样品加标回收率介于91.9%~108.4%,日间相对标准偏差小于14%。
Bibliography:22-1125/O6
SHI Hui,XIA Dan,DENG Xiao-Qing,TAN Yue-Ming,SU Xiao-Li,XIE Qing-Ji,MA Ming(Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Ministry of Education of China,Hunan Normal University,Changsha 410081,China)
A novel method for the determination of sibutramine in dietic teas by dispersive liquid-liquid microextraction-back extraction-solidification of acceptor phase(DLLME-BE-SAP)-high performance liquid chromatography was developed.The optimal experimental conditions were as follows: 400 μL petroleum ether as the organic phase,120 μL methanol as the dispersive solvent,the mixture of 14 μL of 0.2 mol/L HCl and 1 μL methanol as the acceptor phase.The extraction time was 2 min.High enrichment factor(130-fold) of sibutramine was obtained under the optimal experimental conditions.The linear range was 0.6-200 μg/L.The limit of detection(S/N=3) was 0.2 μg/L and the limit of quantitation(S/N=10) was 0.6 μg/L.The recoveries of the spiked samples were from 91.9% to 108.4%,and the inter-da
ISSN:0253-3820
DOI:10.3724/SP.J.1096.2013.30155