首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Rapid and quantitative screening method for 43 benzodiazepines and their metabolites, zolpidem and zopiclone in human plasma by liquid chromatography/mass spectrometry with a small particle column
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Rapid and quantitative screening method for 43 benzodiazepines and their metabolites, zolpidem and zopiclone in human plasma by liquid chromatography/mass spectrometry with a small particle column

机译:小颗粒液相色谱/质谱法快速定量筛选人血浆中43种苯二氮卓类及其代谢产物唑吡坦和佐匹克隆

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摘要

Benzodiazepines and their pharmacologically related drugs, zolpidem and zopiclone are widely prescribed as safe drugs, but these drugs are also abused in cases of crime, suicide and drug-facilitated sexual assault. We developed a rapid and quantitative screening method for 43 benzodiazepines, their metabolites, zolpidem and zopiclone in human plasma by liquid chromatography/mass spectrometry with a small particle column. All drugs were successfully separated within 12 min using combined scan and selected ion recording (SIR) mode. The calibration curves of most drugs were linear in the concentration range 0.5-250 ng/mL with correlation coefficients exceeding 0.99. Within-day precisions (RSD, %) of this method were 1.8-15.6% (10 ng/mL) and 0.6-10.1% (100 ng/mL) and between-day precisions (RSD, %) were 1.6-16.9% (10 ng/mL) and 0.6-16.7% (100 ng/mL). The average recoveries were 70.1% (10 ng/mL) and 87.1% (100 ng/mL). The limit of detection ranged from 0.2 to 8.0 ng/mL in 37 drugs and was below 0.2 ng/mL in 6 drugs. The established method is sensitive and rapid, thus it should be useful in forensic and clinical toxicological analyses.
机译:苯二氮卓类药物及其与药理有关的药物,唑吡坦和佐匹克隆被广泛指定为安全药物,但在犯罪,自杀和以毒品为主导的性侵犯案件中也滥用这些药物。我们开发了一种通过小颗粒液相色谱/质谱法对人体血浆中的43种苯并二氮杂,及其代谢产物,唑吡坦和佐匹克隆进行快速定量筛选的方法。使用组合扫描和选择的离子记录(SIR)模式在12分钟内成功分离了所有药物。大多数药物的校准曲线在0.5-250 ng / mL的浓度范围内呈线性,相关系数超过0.99。该方法的日内精度(RSD,%)为1.8-15.6%(10 ng / mL)和0.6-10.1%(100 ng / mL),日间精度(RSD,%)为1.6-16.9%( 10 ng / mL)和0.6-16.7%(100 ng / mL)。平均回收率为70.1%(10 ng / mL)和87.1%(100 ng / mL)。 37种药物的检出限在0.2到8.0 ng / mL之间,而6种药物的检出限在0.2 ng / mL以下。建立的方法灵敏,快速,因此在法医和临床毒理学分析中应很有用。

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