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出 处:《中国药物滥用防治杂志》2014年第5期270-273,共4页Chinese Journal of Drug Abuse Prevention and Treatment
基 金:公安部重点研究计划项目(201201ZDYJ005)
摘 要:目的:建立了新型“香料”毒品中2种合成大麻素( CP47,497和其同系物 CP47,497(C8))的液相色谱分析方法。方法:以甲醇作为提取溶剂。采用岛津 ODS-SP 型(250mm×4.6mm,5μm)色谱柱,以215nm 作为检测波长。以(甲醇-乙腈)-高纯水为流动相进行梯度洗脱,流速1.2mL/ min,柱温35℃,进样量10μL。结果:在优化条件下,CP47,497和 CP47,497(C8)在1-100μg/ mL 范围内线性良好,相关系数均大于0.9999。方法的检出限(S/ N≥3.3)为0.37μg/ mL 和0.49μg/ mL。日内精密度(相对标准偏差(RSD))为0.82%-1.32%,日间精密度为1.46%-2.11%。CP47,497和 CP47,497(C8)样品溶液在室温下60h 内稳定性良好。结论:方法快速、灵敏、准确、可靠,适用于新型“香料”毒品样本中 CP47,497和 CP47,497(C8)的定量测定。Objective:A high performance liquid chromatographic method was established for determination of CP47,497 and its homologue CP47,497(C8)in novel“spice”drugs. Methods:Methanol was used as the extracting solvent. The separation was per-formed on a Shimadzu ODS-SP column(250mm×4. 6mm,5μm)with gradient elution,using(methanol-acetonitrile)-water as mobile phase. Flow rate was set at 1. 2mL/ min,column temperature was 35℃ and injection volume was 10μL. The detection wavelength of UV detector was set at 215nm. Results:Good linearity was achieved over the range of 1 - 100μg/ mL,with correlation coefficients more than 0. 9999. Limit of detection(S/ N≥3. 3)was 0. 37μg/ mL and 0. 49μg/ mL. The intra-day relative standard deviations(RS-Ds)were 0. 82% - 1. 32% ,and the inter-day RSDs were 1. 46% - 2. 11% . The sample showed stability under room temperature in 60 hours. Conclusion:This method was rapid,sensitive and accurate,and was applicable to quantitative determination of CP47,497 and CP47,497(C8)in novel“Spice”drugs.
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