首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Analysis of eighteen antidepressants, four atypical antipsychotics and active metabolites in serum by liquid chromatography: a simple tool for therapeutic drug monitoring
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Analysis of eighteen antidepressants, four atypical antipsychotics and active metabolites in serum by liquid chromatography: a simple tool for therapeutic drug monitoring

机译:液相色谱法分析血清中的18种抗抑郁药,4种非典型抗精神病药和活性代谢物:监测治疗药物的简单工具

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Therapeutic drug monitoring necessitates efficient, fast and reliable analytical methods validated by external quality control. We therefore devised an isocratic reversed-phase HPLC method with ultraviolet detection and optimised this to quantify mirtazapine, reboxetine, moclobemide, venlafaxine, O-desmethylvenlafaxine, paroxetine, fluvoxamine, fluoxetine, norfluoxetine, sertraline, citalopram, amitriptyline, nortriptyline, imipramine, desipramine, doxepin, nordoxepin, clomipramine, norclomipramine, trimipramine, mianserine, maprotiline, normaprotiline, amisulpride, clozapine, norclozapine, quetiapine, risperidone and 9-OH-risperidone in human serum. After solid-phase extraction of the drugs and metabolites, the chromatographic separation was achieved on a Nucleosil 100-Protect 1 column with acetonitrile-potassium dihydrogenphosphate buffer as mobile phase. The method was validated for therapeutic and toxic serum ranges. A linear relationship (r > 0.998) was obtained between the concentration and the detector signal. Recoveries were between 75 and 99% for the drugs and metabolites. The accuracy of the quality control samples, expressed as percent recovery, ranged from 91 to 118%; intra- and inter-assay-relative standard deviations were 0.9-10.2% and 0.9-9.7%, respectively. Additional external quality control is carried out since 3 years. This method is applicable to rapidly and effectively analyze serum or plasma samples for therapeutic drug monitoring of about 30 antidepressants and atypical antipsychotics.
机译:药物治疗监测需要通过外部质量控制验证的有效,快速和可靠的分析方法。因此,我们设计了一种具有紫外检测的等度反相HPLC方法,并对其进行了优化,以定量米氮平,瑞波西汀,莫氯贝米,文拉法辛,O-去甲基文拉法辛,帕罗西汀,氟伏沙明,氟西汀,正氟西汀,舍曲林,西酞普明,阿米替林,阿米替林,人血清中的多塞平,诺多昔平,氯米帕明,正氯米帕明,曲米帕明,勉强碱,马普替林,去甲丙氨酸,氨磺必利,氯氮平,降氯氮平,喹硫平,利培酮和9-OH-利培酮。固相萃取药物和代谢物后,在Nucleosil 100-Protect 1色谱柱上进行色谱分离,以乙腈-磷酸二氢钾钾缓冲液为流动相。该方法已针对治疗性和毒性血清范围进行了验证。在浓度和检测器信号之间获得线性关系(r> 0.998)。药物和代谢物的回收率在75%至99%之间。以回收率表示的质量控制样品的准确性范围为91%至118%;批内和批间相对标准偏差分别为0.9-10.2%和0.9-9.7%。自3年以来进行了额外的外部质量控制。该方法适用于快速有效地分析血清或血浆样品,以监测约30种抗抑郁药和非典型抗精神病药的治疗药物。

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