首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of 75 abuse drugs including amphetamines, benzodiazepines, cocaine, opioids, piperazines, zolpidem and metabolites in human hair samples using liquid chromatography–tandem mass spectrometry
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Simultaneous determination of 75 abuse drugs including amphetamines, benzodiazepines, cocaine, opioids, piperazines, zolpidem and metabolites in human hair samples using liquid chromatography–tandem mass spectrometry

机译:使用液相色谱 - 串联质谱法同时测定75种滥用药物,包括氨基胺,苯二氮藻,可卡因,阿片类药物,哌嗪,唑类,唑类,唑类,唑类,唑类药物,唑类样品

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Abstract A liquid chromatography–tandem mass spectrometric method for the simultaneous determination of 75 abuse drugs and metabolites, including 19 benzodiazepines, 19 amphetamines, two opiates, eight opioids, cocaine, lysergic acid diethylamide, zolpidem, three piperazines and 21 metabolites in human hair samples, was developed and validated. Ten‐milligram hair samples were decontaminated, pulverized using a ball mill, extracted with 1?mL of methanol spiked with 28 deuterated internal standards in an ultrasonic bath for 60?min at 50°C, and purified with Q‐sep dispersive solid‐phase extraction tubes. The purified extracts were evaporated to dryness and the residue was dissolved in 0.1?mL of 10% methanol. The 75 analytes were analyzed on an Acquity HSS T3 column using gradient elution of methanol and 0.1% formic acid and quantified in multiple reaction monitoring mode with positive electrospray ionization. Calibration curves were linear ( r ?≥?0.9951) from the lower limit of quantitation (2–200?pg/mg depending on the drug) to 2000?pg/mg. The coefficients of variation and accuracy for intra‐ and inter‐assay analysis at three QC levels were 4.3–12.9% and 89.2–109.1%, respectively. The overall mean recovery ranged from 87.1 to 105.3%. This method was successfully applied to the analysis of 11 forensic hair samples obtained from drug abusers.
机译:摘要液相色谱 - 串联质谱法同时测定75个滥用药物和代谢物,包括19个苯二氮卓类药物,19个amphetamines,两种阿片类,八种阿片类药物,可卡因,赖葡萄酒酸二乙基酰胺,唑吡锌矿,三个哌嗪和21种人头样品中的代谢物,开发和验证。使用球磨机粉碎10毫克毛发样品,用球磨机粉碎,用1×ml甲醇萃取,在超声浴中以28次氘代的内标在50℃下掺入60℃,并用Q-Sep分散固相纯化提取管。将纯化的萃取液蒸发至干,将残余物溶于0.1?ml的10%甲醇中。使用甲醇和0.1%甲酸的梯度洗脱分析75分析物在Acquity HSS T3柱上分析,并用阳性电喷雾电离量定量。校准曲线从定量下限(取决于药物的2-200〜pg / mg)到2000〜pg / mg。在三个QC水平下进行测定分析和测定分析的变异系数分别为4.3-12.9%和89.2-109.1%。总体平均恢复范围从87.1到105.3%。该方法成功地应用于从吸毒者获得的11种法医原样的分析。

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