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A screening method for 30 drugs in hair using ultrahigh-performance liquid chromatography time-of-flight mass spectrometry.

机译:使用超高效液相色谱飞行时间质谱法筛选头发中30种药物的方法。

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The objectives of this study were to develop and to validate a qualitative screening method that met the new Society of Hair Testing (SoHT) guideline criteria for thresholds.Extraction of 20 mg hair was performed by a previously validated procedure using overnight incubation in a mixture of methanol:acetonitrile:formiate buffer pH 3 (10:10:80). Analysis was performed on an Agilent 6540 quadrupole time-of-flight mass spectrometer in combination with an Agilent 1290 Infinity ultrahigh-performance liquid chromatography system. Separation was achieved with a 12-minute linear gradient chromatography on a high-strength silica T3 column at acidic conditions. An in-house database containing 30 compounds from the groups amphetamines, opiates, opioids, cocaine, benzodiazepines, and other sedatives including 6 deuterated internal standards was built by analyzing solutions from certified standards. Data were extracted using mass accuracy of ± 10 ppm, retention time deviation of ± 0.15 minutes, and area of ≥ 30,000 counts. Identification was based on scoring of retention time, accurate mass measurement, and isotopic pattern. Validation included selectivity, repeatability of analyte area, and the scoring parameters at the proposed thresholds and a method comparison with the present liquid chromatography-mass spectrometry-mass spectrometry method using 50 authentic hair samples. A daily cutoff calibrator was used to identify positive samples.All cutoffs could be met with imprecisions of less than 5% for most parameters and analytes. Hair from drug-free subjects did not produce any positive results and the method comparison agreed in more than 90% of the cases.We conclude that the developed method meets the criteria of the new SoHT guidelines for screening cutoffs. Even though no thresholds have been suggested for benzodiazepines, we conclude that thresholds between 0.05 and 0.1 ng/mg should be sufficient to determine regular use of these substances.
机译:这项研究的目的是开发并验证一种符合新的头发测试标准(SoHT)阈值准则的定性筛选方法。采用先前验证的方法,使用混合的过夜温育孵育20 mg头发。甲醇:乙腈:甲酸缓冲液pH 3(10:10:80)。分析是在Agilent 6540四极杆飞行时间质谱仪上结合Agilent 1290 Infinity超高效液相色谱系统进行的。在酸性条件下,在高强度硅胶T3色谱柱上使用12分钟的线性梯度色谱法进行分离。通过分析来自认证标准溶液的信息,建立了一个内部数据库,其中包含苯丙胺,阿片类,阿片类药物,可卡因,苯并二氮杂和其他镇静剂等30种化合物,其中包括6种氘代内标。使用±10 ppm的质量准确度,±0.15分钟的保留时间偏差和≥30,000个计数的面积提取数据。鉴定基于保留时间评分,准确的质量测量和同位素模式。验证包括选择性,分析物面积的可重复性以及在建议的阈值处的评分参数,以及与使用50种真实毛发样品的本液相色谱-质谱-质谱法进行的方法比较。每天使用截断校准品来鉴定阳性样品,对于大多数参数和分析物,所有截断的准确度均低于5%。来自无毒品受试者的头发没有产生任何阳性结果,并且在90%以上的病例中方法比较均得到了认可。我们得出的结论是,所开发的方法符合新的SoHT筛选临界值的标准。即使没有建议苯二氮卓类的阈值,但我们得出的结论是0.05到0.1 ng / mg之间的阈值应该足以确定这些物质的常规使用。

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