首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Development and validation of a liquid chromatography mass spectrometry assay for the simultaneous quantification of methadone, cocaine, opiates and metabolites in human umbilical cord
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Development and validation of a liquid chromatography mass spectrometry assay for the simultaneous quantification of methadone, cocaine, opiates and metabolites in human umbilical cord

机译:液相色谱质谱分析法的开发和验证,用于同时定量人脐带中的美沙酮,可卡因,鸦片制剂和代谢物

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摘要

A liquid chromatography mass spectrometric selected reaction monitoring mode (SRM) method for methadone, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), cocaine, benzoylecgonine (BE), 6-acetylmorphine, morphine and codeine quantification in human umbilical cord was developed and fully validated. Analytes were extracted from homogenized tissue (1 g) by solid phase extraction. Linearity was 2.5-500 ng/g, except for methadone (10-2000 ng/g). Method imprecision was <12.7%CV with analytical recovery 85.9-112.7%, extraction efficiency >59.2%, matrix effect 4.5-39.5%, process efficiency 48.6-92.6% and stability >84.6%. Analysis of an umbilical cord following controlled methadone administration and illicit drug use contained in ng/g, 40.3 morphine, 3.6 codeine, 442 BE, 186 methadone and 45.9 EDDP.
机译:液相色谱质谱选择反应监测模式(SRM)方法用于美沙酮,2-亚乙基-1,5-二甲基-3,3-二苯基吡咯烷(EDDP),可卡因,苯甲酰芽子碱(BE),6-乙酰基吗啡,吗啡和可待因定量在人类脐带中的开发和充分验证。通过固相萃取从均质的组织(1 g)中萃取分析物。除美沙酮(10-2000 ng / g)外,线性为2.5-500 ng / g。方法不精确度为<12.7%CV,分析回收率为85.9-112.7%,萃取效率> 59.2%,基质效应为4.5-39.5%,过程效率为48.6-92.6%,稳定性为> 84.6%。 ng / g,40.3吗啡,3.6可待因,442 BE,186美沙酮和45.9 EDDP中所含美沙酮的控制给药和非法药物使用后的脐带分析。

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