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高效液相色谱-电喷雾电离质谱法(HPLC-MS/ESI)同时测定血浆中的氟西汀、西酞普兰、帕罗西汀和文拉法辛。

Simultaneous determination of fluoxetine, citalopram, paroxetine, venlafaxine in plasma by high performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-MS/ESI).

作者信息

Juan He, Zhiling Zhou, Huande Li

机构信息

Clinical Pharmaceutical Research Institute, Second Xiangya Hospital, Central South University, Changsha 410011, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Jun 5;820(1):33-9. doi: 10.1016/j.jchromb.2005.03.006. Epub 2005 Apr 11.

Abstract

UNLABELLED

Fluoxetine, citalopram, paroxetine and venlafaxine have been widely used in the treatment of depression. However, no study has been conducted to determine the four drugs simultaneously by high performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-MS/ESI).

OBJECTIVE

To establish a new, rapid and sensitive HPLC-MS/ESI method for simultaneous determination and screening in human plasma of the four most commonly prescribed nontricyclic antidepressants: fluoxetine, citalopram, paroxetine and venlafaxine.

METHODS

The analytes in plasma were extracted by solid-phase-extraction column after samples had been alkalinized. The HPLC separation of the analytes was performed on a MACHEREY-NAGEL C(18) (250 mmx4.6 mm, 5 microm, Germany) column, using water (formic acid 0.6 per thousand, ammonium acetate: 30 mmol/l)-acetonitrile (35:65, v/v) as mobile phase, with a flow-rate of 0.85 ml/min. The compounds were ionized in the electrospray ionization (ESI) ion source of the mass spectrometer and were detected in the selected ion recording (SIR) mode.

RESULTS

The calibration curves were linear in the 5.0-1000.0 ng/ml range for all compounds, all of them with coefficients of determination above 0.9900. The average extraction recoveries for all the four analytes were above 73.2%. The methodology recoveries were higher than 95.0%. The limits of detection (LODs) were 0.5, 0.3, 0.3 and 0.1 ng/ml for fluoxetine, citalopram, paroxetine and venlafaxine, respectively. The intra- and inter-day variation coefficients were less than 15.0%.

CONCLUSION

The method is accurate, sensitive and simple for routine therapeutic drug monitoring (TDM) as well as toxicologic screening, and for the study of the pharmacokinetics and metabolism of the four drugs.

摘要

未标注

氟西汀、西酞普兰、帕罗西汀和文拉法辛已广泛用于治疗抑郁症。然而,尚未有研究采用高效液相色谱 - 电喷雾电离质谱法(HPLC - MS/ESI)同时测定这四种药物。

目的

建立一种新的、快速且灵敏的HPLC - MS/ESI方法,用于同时测定和筛选人血浆中四种最常用的非三环类抗抑郁药:氟西汀、西酞普兰、帕罗西汀和文拉法辛。

方法

样品碱化后,血浆中的分析物通过固相萃取柱进行萃取。分析物的HPLC分离在MACHEREY - NAGEL C(18)(250 mm×4.6 mm,5μm,德国)柱上进行,以水(甲酸0.6‰,醋酸铵:30 mmol/l) - 乙腈(35:65,v/v)作为流动相,流速为0.85 ml/min。化合物在质谱仪的电喷雾电离(ESI)离子源中电离,并在选择离子记录(SIR)模式下进行检测。

结果

所有化合物的校准曲线在5.0 - 1000.0 ng/ml范围内呈线性,它们的决定系数均高于0.9900。四种分析物的平均萃取回收率均高于73.2%。方法回收率高于95.0%。氟西汀、西酞普兰、帕罗西汀和文拉法辛的检测限(LOD)分别为0.5、0.3、0.3和0.1 ng/ml。日内和日间变异系数均小于15.0%。

结论

该方法准确、灵敏且简便,适用于常规治疗药物监测(TDM)以及毒理学筛查,也适用于这四种药物的药代动力学和代谢研究。

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