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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Development of a new multi-analyte assay for the simultaneous detection of opioids in serum and other body fluids using liquid chromatography-tandem mass spectrometry
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Development of a new multi-analyte assay for the simultaneous detection of opioids in serum and other body fluids using liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法同时检测血清和其他体液中阿片类药物的新的多分析物测定方法的开发

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A liquid chromatography-tandem mass spectrometry method using electrospray ionization in positive ionization mode was developed for the simultaneous detection of multiple opioid-type drugs in plasma. The presented assay allows the quantitative determination of alfentanil, buprenorphine, codeine, desomorphine, dextromethorphan, dextrorphan, dihydrocodeine, dihydromorphine, ethylmorphine, fentanyl, hydrocodone, hydromorphone, methadone, morphine, naloxone, naltrexone, oxycodone, oxymorphone, pentazocine, pethidine, pholcodine, piritramide, remifentanil, sufentanil, and tramadol as well as the metabolites 6-monoacetylmorphine, bisnortilidine, morphine-3-glucuronide, morphine-6-glucuronide, naltrexol, norbuprenorphine, norfentanyl, norpethidine, nortilidine, and O-desmethyltramadol. Serum and blood samples were purified by solid-phase extraction. The analytes were separated on a phenyl-hexyl (100 mm) column by formic acid/acetonitrile gradient elution using an UPLC 1290 Infinity coupled with a 6490 Triple Quadrupole mass spectrometer. The limits of detection ranged from 0.02 to 0.6 ng/mL and the lower limits of quantification ranged from 0.1 to 2.0 ng/mL. The calibration curves were linear between Calibration Levels 1-6 for all 35 substances. Recovery rates ranged between 51 and 88% for all compounds except alfentanil, bisnortilidine, pethidine, and morphine-3-glucuronide. The matrix effect ranged from 86% for ethylmorphine to 105% for desomorphine. Using the validation procedure proposed by the German Society ofToxicological and Forensic Chemistry, acceptable precision and accuracy data for almost all analytes were obtained. The method was successfully applied to 206 authentic serum samples provided by the palliative and intensive care units of the University Medical Center and the police authorities. Furthermore, a suspected fatal intoxication is demonstrated by an analysis of the sufentanil in post mortem body fluids and tissues. (C) 2015 Elsevier B.V. All rights reserved.
机译:为了同时检测血浆中多种阿片类药物,开发了一种以正电离模式使用电喷雾电离的液相色谱-串联质谱方法。提出的测定方法可以定量测定阿芬太尼,丁丙诺啡,可待因,去甲吗啡,右美沙芬,右美沙芬,二氢可待因,二氢吗啡,乙基吗啡,芬太尼,氢可待因酮,氢吗啡酮,美沙酮,吗啡,纳洛酮,纳曲酮,羟考酮,哌替啶,羟考酮,吡咯乙酰胺,瑞芬太尼,舒芬太尼和曲马多,以及代谢物6-单乙酰吗啡,双去甲替丁,吗啡-3-葡糖醛酸,吗啡-6-葡糖醛酸,纳曲醇,去甲丁丙诺啡,去甲芬太尼,降冰片烷,降冰片啶和O-去甲基曲马多。通过固相提取纯化血清和血液样品。使用UPLC 1290 Infinity和6490三重四极杆质谱仪,通过甲酸/乙腈梯度洗脱,在苯己基(100 mm)色谱柱上分离分析物。检测限为0.02至0.6 ng / mL,定量下限为0.1至2.0 ng / mL。对于所有35种物质,校准曲线在1-6级校准之间是线性的。除阿芬太尼,双去甲替丁,哌替啶和吗啡-3-葡糖醛酸以外的所有化合物的回收率在51%至88%之间。基质效应的范围从乙基吗啡的86%到去甲吗啡的105%。使用德国毒理学和法医学会提出的验证程序,可以获得几乎所有分析物可接受的精度和准确度数据。该方法已成功应用于大学医学中心和警察当局的姑息治疗和重症监护室提供的206个真实血清样品。此外,尸检后体液和组织中舒芬太尼的分析证明可疑致命性中毒。 (C)2015 Elsevier B.V.保留所有权利。

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