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采用固相萃取和气相色谱/质谱联用技术同时定量测定人血浆中的哌替啶、去甲哌替啶、曲马多、丙氧芬和去甲丙氧芬:方法验证及其在治疗剂量心血管安全性中的应用

Simultaneous quantitation of meperidine, normeperidine, tramadol, propoxyphene and norpropoxyphene in human plasma using solid-phase extraction and gas chromatography/mass spectrometry: Method validation and application to cardiovascular safety of therapeutic doses.

作者信息

Fernández Nicolás, Olivera Nancy Mónica, Keller Guillermo Alberto, Diez Roberto Alberto, Di Girolamo Guillermo, Quiroga Patricia Noemí

机构信息

Facultad de Farmacia y Bioquímica, Cátedra de Toxicología y Química Legal, Laboratorio de asesoramiento toxicológico analítico (CENATOXA). Junín 956 7mo piso (C1113AAD). Ciudad Autónoma de Buenos Aires (CABA), Universidad de Buenos Aires, Buenos Aires, Argentina.

Facultad de Medicina, Segunda Cátedra de Farmacología. Paraguay 2155 16avopiso (C1221ABG), Ciudad Autónoma de Buenos Aires (CABA), Universidad de Buenos Aires, Buenos Aires, Argentina.

出版信息

Rapid Commun Mass Spectrom. 2017 Sep 30;31(18):1519-1533. doi: 10.1002/rcm.7933.

Abstract

RATIONALE

Several opioid analgesics have been related to the prolongation of cardiac repolarization, a condition which can be fatal. In order to establish a correct estimation of the risk/benefit balance of therapeutic doses of meperidine, normeperidine, tramadol, propoxyphene and norpropoxyphene, it was necessary to develop an analytical method to determinate plasma concentrations of these opioids.

METHODS

Here we describe a method which incorporates strong alkaline treatment to obtain norpropoxyphene amide followed by a one-elution step solid-phase extraction, and without further derivatization. Separation and quantification were achieved by gas chromatography/electron ionization mass spectrometry (GC/EI-MS) in selected-ion monitoring mode. Quantification was performed with 500 μL of plasma by the addition of deuterated analogues as internal standards.

RESULTS

The proposed method has been validated in the linearity range of 25-1000 ng/mL for all the analytes, with correlation coefficients higher than 0.990. The lower limit of quantification was 25 ng/mL. The intra- and inter-day precision, calculated in terms of relative standard deviation, were 2.0-12.0% and 6.0-15.0%, respectively. The accuracy, in terms of relative error, was within a ± 10% interval. The absolute recovery and extraction efficiency ranged from 81.0 to 111.0% and 81.0 to 105.0%, respectively.

CONCLUSIONS

A GC/MS method for the rapid and simultaneous determination of meperidine, normeperidine, tramadol, propoxyphene and norpropoxyphene in human plasma was developed, optimized and validated. This procedure was shown to be sensitive and specific using small specimen amounts, suitable for application in routine analysis for forensic purposes and therapeutic monitoring. To our knowledge, this is the first full validation of the simultaneous determination of these opioids and their metabolites in plasma samples.

摘要

原理

几种阿片类镇痛药与心脏复极化延长有关,这种情况可能是致命的。为了正确评估哌替啶、去甲哌替啶、曲马多、丙氧芬和去甲丙氧芬治疗剂量的风险/效益平衡,有必要开发一种分析方法来测定这些阿片类药物的血浆浓度。

方法

我们在此描述一种方法,该方法采用强碱处理以获得去甲丙氧芬酰胺,随后进行一步洗脱固相萃取,且无需进一步衍生化。通过气相色谱/电子电离质谱(GC/EI-MS)在选择离子监测模式下实现分离和定量。通过添加氘代类似物作为内标,对500 μL血浆进行定量。

结果

所提出的方法在所有分析物25 - 1000 ng/mL的线性范围内得到验证,相关系数高于0.990。定量下限为25 ng/mL。以相对标准偏差计算的日内和日间精密度分别为2.0 - 12.0%和6.0 - 15.0%。以相对误差表示的准确度在±10%区间内。绝对回收率和提取效率分别为81.0%至111.0%和81.0%至105.0%。

结论

开发、优化并验证了一种用于快速同时测定人血浆中哌替啶、去甲哌替啶、曲马多、丙氧芬和去甲丙氧芬的GC/MS方法。该方法使用少量样本显示出灵敏性和特异性,适用于法医目的的常规分析和治疗监测。据我们所知,这是首次对血浆样本中这些阿片类药物及其代谢物的同时测定进行全面验证。

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