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作 者:张小婷[1] 孙立敏[1] 刘娟[1] 徐淑云[1]
机构地区:[1]广州市刑事科学技术研究所,广东广州510030
出 处:《中国法医学杂志》2011年第1期16-18,共3页Chinese Journal of Forensic Medicine
摘 要:目的建立SPE/UPLC方法在同一条件下同时检测血中吗啡、苯丙胺类及氯胺酮。方法采用SCX 3cc(60mg)固相萃取柱萃取血中吗啡、MA、MDMA、MDA及氯胺酮,用超高效液相色谱(UPLC)-二极管阵列检测器(PDA)检测,结合保留时间和紫外光谱进行定性、定量分析,对实验各环节进行优化,并进行实际案例检测。结果吗啡、MA、MDMA、MDA、氯胺酮的固相萃取提取回收率分别为81.4%±2.51%、88.2%±2.48%、91.8%±2.03%、93.8%±1.46%、74.8%±2.27%,峰面积和质量浓度的线性关系良好(r>0.999),线性范围分别为0.08~100μg/mL、0.4~100μg/mL、0.2~75μg/mL、0.3~75μg/mL、0.4~100μg/mL,检出限分别为30pg、200pg、80pg、100pg、200pg。结论本文所建方法适用于血中吗啡、苯丙胺类、氯胺酮常见毒品的筛选及定量分析。Objective To establish a solid phase extraction(SPE)/UPLC method for the determination of morphine,amphetamines and ketamine in whole blood simultaneously.Methods Morphine,MA,MDMA,MDA,ketamine were extracted from whole blood using Agilent SCX 3cc(60mg)extraction cartridges and detected by UPLC-PDA.Qualitative and quantitative analysis was obtained by retention time and UV-spectrum.Results The recoveries for morphine,MA,MDMA,MDA,ketamine were 81.4%±2.51%,88.2%±2.48%,91.8%±2.03%,93.8%±1.46%,74.8%±2.27% respectively,The correlation coefficient of linear calibration curve was over 0.999 within concentration range 0.08~100μg/mL,0.4~100μg/mL,0.2~75μg/mL,0.3~75μg/mL,0.4~100μg/mL respectively.The limits of qualification were 30pg,200pg,80pg,100pg,200pg respectively.Conclusion The method was simple,rapid and accurate for qualitative and quantitative analysis of morphine,amphetamines,ketamine in whole blood simultaneously.
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