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Quantification of Synthetic Cathinones in Rat Brain Using HILIC–ESI-MS/MS

机译:使用HILIC-ESI-MS / MS对大鼠脑中合成的卡西酮进行定量

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摘要

The abuse of synthetic cathinones, formerly marketed as “bath salts”, has emerged over the last decade. Three common drugs in this class include 3,4-methylenedioxypyrovalerone (MDPV), 4-methylmethcathinone (mephedrone), and 3,4-methylenedioxymethcathinone (methylone). An LC–MS/MS method has been developed and validated for the simultaneous quantification of MDPV, mephedrone, and methylone in brain tissue. Briefly, MDPV, mephedrone, methylone, and their deuterium-labeled analogs were subjected to solid phase extraction (SPE) and separated using an HILIC Silica Column. The HPLC was coupled to a Shimadzu IT-TOF (ion trap-time of flight) system with the electrospray source running in positive mode (+ESI). The method was validated for precision, accuracy, and extraction efficiency. All inter-day and intra-day % RSD (percent relative standard deviation) and % error values were less than 15% and extraction efficiency exceeded 80%. These conditions allowed for limits of detection of 1ng/mL for MDPV, and 5 ng/mL for both mephedrone and methylone. The limits of quantification were determined to be 5ng/mL for MDPV and 10 ng/mL for mephedrone and methylone. The method was utilized to evaluate the pharmacokinetics of these drugs in adult male rats following administration of a drug cocktail including MDPV, mephedrone, and methylone. All three compounds reached peak concentrations in the brain within 15 min. Although methylone and mephedrone were administered at the same dose, the peak concentration (Cmax) of mephedrone in the brain was significantly higher than that for methylone, as was the area under the curve (AUC). In summary, this quick and sensitive method for measuring synthetic cathinones may be used for future pharmacokinetic investigations of these drugs in target tissue.
机译:在过去的十年中,滥用合成的卡西酮(以前称为“沐浴盐”)开始出现。此类中的三种常见药物包括3,4-亚甲基二氧吡咯烷酮(MDPV),4-甲基甲卡西酮(甲氧麻黄酮)和3,4-亚甲基二氧甲卡西酮(甲酮)。已经开发出一种LC-MS / MS方法,并且该方法可以同时定量测定脑组织中的MDPV,甲氧麻黄酮和甲酮。简而言之,将MDPV,甲吗啡酮,甲酮及其氘标记的类似物进行固相萃取(SPE),并使用HILIC硅胶柱进行分离。 HPLC与Shimadzu IT-TOF(离子阱飞行时间)系统耦合,电喷雾源以正模式(+ ESI)运行。验证了该方法的准确性,准确性和提取效率。所有日间和日内%RSD(相对标准偏差百分比)和%误差值均小于15%,提取效率超过80%。这些条件使得对MDPV的检出限为1ng / mL,对甲氧麻黄酮和甲酮的检出限为5 ng / mL。定量限确定为MDPV为5ng / mL,甲氧麻黄酮和甲酮为10ng / mL。该方法用于评估这些药物在给药包括MDPV,甲氧麻黄酮和甲酮的药物混合物后在成年雄性大鼠中的药代动力学。所有三种化合物在15分钟内达到大脑中的峰值浓度。尽管甲酮和甲氧麻黄酮以相同的剂量给药,但脑中甲氧麻黄酮的峰值浓度(Cmax)明显高于甲酮的峰值浓度(Cmax),曲线下面积(AUC)也是如此。总之,这种用于测量合成卡西酮的快速而灵敏的方法可用于将来在靶组织中对这些药物进行药代动力学研究。

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