首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >The quantitative analysis of heroin, methadone and their metabolites and the simultaneous detection of cocaine, acetylcodeine and their metabolites in human plasma by high-performance liquid chromatography coupled with tandem mass spectrometry
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The quantitative analysis of heroin, methadone and their metabolites and the simultaneous detection of cocaine, acetylcodeine and their metabolites in human plasma by high-performance liquid chromatography coupled with tandem mass spectrometry

机译:高效液相色谱-串联质谱法定量分析海洛因,美沙酮及其代谢物并同时检测人血浆中的可卡因,乙酰可待因及其代谢物

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For a pharmacokinetic-pharmacodynamic study in opioid tolerant patients, who were treated with heroin in combination with methadone, a liquid chromatographic assay with tandem mass spectrometry detection (LC-MS/MS) was developed for the simultaneous determination of heroin, methadone, heroin metabolites 6-monoacetylmorphine, morphine, and morphine-6 and 3-glucuronide and methadone metabolite EMDP. To detect any abuse of substances besides the prescribed opioids the assay was extended with the detection of cocaine, its metabolites benzoylecgonine and norcocaine and illicit heroin adulterants acetylcodeine and codeine. Heroin-d6, morphine-d3, morphine-3-glucuronide-d3 and methadone-d9 were used as internal standards. The sample pre-treatment consisted of solid phase extraction using mixed mode sorbent columns (MCX Oasis). Chromatographic separation was performed at 25 degrees C on a reversed phase Zorbax column with a gradient mobile phase consisting of ammonium formate (pH 4.0) and acetonitrile. The run time was 15 min. MS with relatively mild electrospray ionisation under atmospheric pressure was applied. The triple quadrupole MS was operating in the positive ion mode and multiple reaction monitoring (MRM) was used for drug quantification. The method was validated over a concentration range of 5-500 ng/mL for all analytes. The total recovery of heroin varied between 86 and 96% and of the heroin metabolites between 76 and 101%. lntra-assay and inter-assay accuracy and precision of all analytes were always within the designated limits (<= 20% at lower limit of quantification (LLQ) and <= 15% for other samples). This specific and sensitive assay was successfully applied in pharmacokinetic studies with medically prescribed heroin and toxicological cases. (c) 2005 Elsevier B.V. All rights reserved.
机译:为了对接受海洛因联合美沙酮治疗的阿片耐受性患者进行药代动力学研究,开发了一种液相色谱-串联质谱检测法(LC-MS / MS),用于同时测定海洛因,美沙酮,海洛因代谢物6-单乙酰吗啡,吗啡,吗啡-6和3-葡糖醛酸苷和美沙酮代谢物EMDP。为了检测除规定的阿片类药物以外的任何滥用药物,该检测方法还扩展了可卡因,其代谢产物苯甲酰芽子碱和去甲可卡因以及非法海洛因掺杂物乙酰可待因和可待因的检测。海洛因-d6,吗啡-d3,吗啡-3-葡萄糖醛酸-d3和美沙酮-d9被用作内标。样品预处理包括使用混合模式吸附柱(MCX Oasis)进行固相萃取。在反相的Zorbax色谱柱上于25摄氏度下进行色谱分离,其中梯度流动相由甲酸铵(pH 4.0)和乙腈组成。运行时间为15分钟。使用在大气压下具有相对温和的电喷雾电离的MS。三重四极杆质谱仪以正离子模式运行,并且使用多反应监测(MRM)进行药物定量。对于所有分析物,该方法均在5-500 ng / mL的浓度范围内得到验证。海洛因的总回收率在86%至96%之间,海洛因代谢产物的回收率在76%至101%之间。所有分析物的测定内和测定间准确性和精密度始终在指定的范围内(在定量下限(LLQ)下,<= 20%,其他样品<= 15%)。这种特异性和灵敏的测定方法已成功用于药物处方的海洛因和毒理学病例的药代动力学研究。 (c)2005 Elsevier B.V.保留所有权利。

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