Liqun Zhang1, Pinggu Wu2, Quan Jin1, Zhengyan Hu3, Junlin Wang3. 1. Center for Disease Control and Prevention of Hangzhou, Hangzhou 310021, PR China. 2. Center for Disease Control and Prevention of Zhejiang Province, Hangzhou 310009, PR China. Electronic address: pgwu@cdc.zj.cn. 3. Center for Disease Control and Prevention of Zhejiang Province, Hangzhou 310009, PR China.
Abstract
BACKGROUND: Sedative drugs are often used for the treatment of depression, anxiety and insomnia and they are involved in many forensic cases. This work established a method for the simultaneous determination of multi-groups of sedative drugs (benzodiazepines, barbitals, phenothiazines, tricyclic antidepressant and butyrophenone) in human plasma for forensic analysis. A large number of sedative drugs with forensic interest can be analyzed in a short time with lower limits of quantification by combination of SPE extraction and ultra performance liquid chromatography-tandem mass spectrometry. METHODS: Sample preparation consisted of extraction of the plasma by hydrochloric acid solution and further purified by SLW solid phase extraction column. RESULTS: The method was fully validated to cover large concentration ranges of 50-1000μg/L for 5 Barbital drugs, while 1.0-50μg/L for the other 14 sedative drugs. The average recoveries of the drugs spiked at three levels ranged from 65.3% to 114.3% with the relative standard deviation between 1.2% and 13.2%. The lowest limits of quantification (LLOQ) were 100μg/L for Barbital drugs and1.0μg/L for all the other 14 drugs. CONCLUSIONS: This validated method has been successfully used in emergency analysis of multi-residues of sedative drugs in plasma.
BACKGROUND: Sedative drugs are often used for the treatment of depression, anxiety and insomnia and they are involved in many forensic cases. This work established a method for the simultaneous determination of multi-groups of sedative drugs (benzodiazepines, barbitals, phenothiazines, tricyclic antidepressant and butyrophenone) in human plasma for forensic analysis. A large number of sedative drugs with forensic interest can be analyzed in a short time with lower limits of quantification by combination of SPE extraction and ultra performance liquid chromatography-tandem mass spectrometry. METHODS: Sample preparation consisted of extraction of the plasma by hydrochloric acid solution and further purified by SLW solid phase extraction column. RESULTS: The method was fully validated to cover large concentration ranges of 50-1000μg/L for 5 Barbital drugs, while 1.0-50μg/L for the other 14 sedative drugs. The average recoveries of the drugs spiked at three levels ranged from 65.3% to 114.3% with the relative standard deviation between 1.2% and 13.2%. The lowest limits of quantification (LLOQ) were 100μg/L for Barbital drugs and1.0μg/L for all the other 14 drugs. CONCLUSIONS: This validated method has been successfully used in emergency analysis of multi-residues of sedative drugs in plasma.