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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination in hair of multiclass drugs of abuse (including THC) by ultra-high performance liquid chromatography-tandem mass spectrometry
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Simultaneous determination in hair of multiclass drugs of abuse (including THC) by ultra-high performance liquid chromatography-tandem mass spectrometry

机译:超高效液相色谱-串联质谱法同时测定头发中多种滥用药物(包括四氢大麻酚)

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摘要

A simple procedure for the quantitative determination in hair samples of 13 common drugs of abuse or metabolites (morphine, 6-acetylmorphine, codeine, amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine, 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyethylamphetamine, benzoylecgonine, cocaine, buprenorphine, methadone and Δ 9-tetrahydrocannabinol) has been developed and fully validated. The analytes were extracted from the matrix by a simple overnight incubation with methanol at 55°C. An aliquot of the extract was directly injected into an ultra-high performance liquid chromatography system equipped with Waters Acquity UHPLC BEH C18 column (100mm×2.1mm, 1.7μm). The mobile phase eluted with a linear gradient (water/formic acid 5mM:acetonitrile; v:v) from 98:2 to 0:100 in 4.5min, followed by isocratic elution at 100% B for 1.0min. The flow rate was 0.6mL/min and the total run time was 8.0min including re-equilibration at the initial conditions. The compounds were revealed by a triple quadrupole mass spectrometer operating in the selected reaction monitoring mode. The absence of matrix interferents, together with excellent repeatability of both retention times and relative abundances of diagnostic transitions, allowed the correct identification of all analytes tested. The method proved linear in the interval from the limit of quantification to 5.0ng/mg (1.0ng/mg for Δ ~9-tetrahydrocannabinol) with correlation coefficient values ranging from 0.9970 to 0.9997. Quantitation limits were below the cut-off values recommended by the Society of Hair Testing and ranged from 0.02 to 0.08ng/mg. Application of the present UHPLC-MS/MS procedure and instrumentation to hair analysis allows high sample-throughput, together with excellent sensitivity and selectivity, in workplace drug-screening controls and forensic investigations. These qualities, combined with minimal sample workup, make the cost of this screening affordable for most private and public administrations.
机译:定量测定头发样品中13种常见滥用药物或代谢物的简单方法(吗啡,6-乙酰吗啡,可待因,苯丙胺,甲基苯丙胺,3,4-亚甲基二氧苯丙胺,3,4-亚甲基二氧甲基苯丙胺,3,4-亚甲基二氧乙基苯丙胺,苯甲酰芽子碱,可卡因,丁丙诺啡,美沙酮和Δ9-四氢大麻酚已开发并得到充分验证。通过在55°C与甲醇的简单过夜孵育,从基质中提取分析物。将提取的等分试样直接注入配备有Waters Acquity UHPLC BEH C18色谱柱(100mm×2.1mm,1.7μm)的超高效液相色谱系统中。流动相在4.5分钟内从98:2到0:100进行线性梯度洗脱(水/甲酸5mM:乙腈; v:v),然后在100%B下等度洗脱1.0分钟。流速为0.6mL / min,包括在初始条件下重新平衡在内的总运行时间为8.0min。通过在选定的反应监测模式下运行的三重四极杆质谱仪显示化合物。基质干扰物的不存在,以及保留时间和诊断转换的相对丰度都具有出色的可重复性,可以正确鉴定所有测试的分析物。该方法在定量限至5.0ng / mg(对于Δ〜9-四氢大麻酚为1.0ng / mg)的区间内证明是线性的,相关系数范围为0.9970至0.9997。定量限低于头发测试协会推荐的临界值,范围为0.02至0.08ng / mg。本UHPLC-MS / MS方法和仪器在头发分析中的应用可在工作场所药物筛选控制和法医研究中实现高样品通量,并具有出色的灵敏度和选择性。这些质量加上最少的样品检查,使大多数私人和公共管理部门负担得起这种筛查的费用。

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