Rook Elisabeth J, Hillebrand Michel J X, Rosing Hilde, van Ree Jan M, Beijnen Jos H
Slotervaart Hospital, Department of Pharmacy and Pharmacology, Louwesweg 6, P.O. Box 90440, 1006 BK Amsterdam, The Netherlands.
J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Sep 25;824(1-2):213-21. doi: 10.1016/j.jchromb.2005.05.048.
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%. Intra-assay and inter-assay accuracy and precision of all analytes were always within the designated limits (< or =20% at lower limit of quantification (LLQ) and < or =15% for other samples). This specific and sensitive assay was successfully applied in pharmacokinetic studies with medically prescribed heroin and toxicological cases.
对于一项针对阿片类药物耐受患者的药代动力学-药效学研究(这些患者接受海洛因与美沙酮联合治疗),开发了一种采用串联质谱检测的液相色谱法(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-葡萄糖醛酸苷以及美沙酮代谢物EMDP。为检测除规定阿片类药物之外的任何物质滥用情况,该检测方法扩展至检测可卡因、其代谢物苯甲酰爱康宁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。海洛因-d6、吗啡-d3、吗啡-3-葡萄糖醛酸苷-d3和美沙酮-d9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25℃下,于反相Zorbax柱上进行色谱分离,流动相为梯度洗脱,由甲酸铵(pH 4.0)和乙腈组成。运行时间为15分钟。采用大气压下相对温和的电喷雾电离质谱法。三重四极杆质谱在正离子模式下运行,多反应监测(MRM)用于药物定量分析。该方法在5-500 ng/mL的浓度范围内对所有分析物进行了验证。海洛因的总回收率在86%至96%之间,海洛因代谢物的总回收率在76%至101%之间。所有分析物的批内和批间准确度及精密度始终在规定限度内(定量下限(LLQ)处≤20%,其他样品≤15%)。这种特异性和灵敏的检测方法已成功应用于医学处方海洛因的药代动力学研究及毒理学案例分析。