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采用超高效液相色谱串联质谱法测定血浆和尿液中羟考酮及其主要代谢产物去甲羟考酮和羟吗啡酮:在实际案例中的应用

Determination of oxycodone and its major metabolites noroxycodone and oxymorphone by ultra-high-performance liquid chromatography tandem mass spectrometry in plasma and urine: application to real cases.

作者信息

Pantano Flaminia, Brauneis Stefano, Forneris Alexandre, Pacifici Roberta, Marinelli Enrico, Kyriakou Chrystalla, Pichini Simona, Busardò Francesco Paolo

机构信息

.

出版信息

Clin Chem Lab Med. 2017 Aug 28;55(9):1324-1331. doi: 10.1515/cclm-2016-0990.

Abstract

BACKGROUND

Oxycodone is a narcotic drug widely used to alleviate moderate and severe acute and chronic pain. Variability in analgesic efficacy could be explained by inter-subject variations in plasma concentrations of parent drug and its active metabolite, oxymorphone. To evaluate patient compliance and to set up therapeutic drug monitoring (TDM), an ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) assay was developed and validated for the parent drug and its major metabolites noroxycodone and oxymorphone.

METHODS

Extraction of analytes from plasma and urine samples was obtained by simple liquid-liquid extraction. The chromatographic separation was achieved with a reversed phase column using a linear gradient elution with two solvents: acetic acid 1% in water and methanol. The separated analytes were detected with a triple quadrupole mass spectrometer operated in multiple reaction monitoring (MRM) mode via positive electrospray ionization (ESI).

RESULTS

Separation of analytes was obtained in less than 5 min. Linear calibration curves for all the analytes under investigation in urine and plasma samples showed determination coefficients (r2) equal or higher than 0.990. Mean absolute analytical recoveries were always above 86%. Intra- and inter-assay precision (measured as coefficient of variation, CV%) and accuracy (measured as % error) values were always better than 13%. Limit of detection at 0.06 and 0.15 ng/mL and limit of quantification at 0.2 and 0.5 ng/mL for plasma and urine samples, respectively, were adequate for the purpose of the present study.

CONCLUSIONS

Rapid extraction, identification and quantification of oxycodone and its metabolites both in urine and plasma by UHPLC-MS/MS assay was tested for its feasibility in clinical samples and provided excellent results for rapid and effective drug testing in patients under oxycodone treatment.

摘要

背景

羟考酮是一种广泛用于缓解中度和重度急慢性疼痛的麻醉药物。母体药物及其活性代谢产物羟吗啡酮血浆浓度的个体间差异可以解释镇痛效果的变异性。为了评估患者依从性并建立治疗药物监测(TDM),开发并验证了一种超高效液相色谱-串联质谱(UHPLC-MS/MS)法,用于检测母体药物及其主要代谢产物去甲羟考酮和羟吗啡酮。

方法

通过简单的液-液萃取从血浆和尿液样本中提取分析物。采用反相柱,使用两种溶剂(1%乙酸水溶液和甲醇)进行线性梯度洗脱实现色谱分离。分离后的分析物通过正电喷雾电离(ESI)在多反应监测(MRM)模式下由三重四极杆质谱仪进行检测。

结果

在不到5分钟内实现了分析物的分离。尿液和血浆样本中所有被研究分析物的线性校准曲线的决定系数(r2)均等于或高于0.990。平均绝对分析回收率始终高于86%。批内和批间精密度(以变异系数,CV%衡量)和准确度(以%误差衡量)值始终优于13%。血浆和尿液样本的检测限分别为0.06和0.15 ng/mL,定量限分别为0.2和0.5 ng/mL,足以满足本研究的目的。

结论

通过UHPLC-MS/MS法对尿液和血浆中的羟考酮及其代谢产物进行快速提取、鉴定和定量,在临床样本中测试了其可行性,并为羟考酮治疗患者的快速有效药物检测提供了优异结果。

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