首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Quantification of peramivir in dog plasma by liquid chromatography/tandem mass spectrometry employing precolumn derivatization
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Quantification of peramivir in dog plasma by liquid chromatography/tandem mass spectrometry employing precolumn derivatization

机译:采用柱前衍生化的液相色谱/串联质谱法定量狗血浆中的帕拉米韦

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摘要

Peramivir is a novel influenza neuraminidase inhibitor used for anti-influenza. In this article, a novel method was developed to determine peramivir in dog plasma using a derivatization treatment step to increase the retention time and enhance the signal intensity. The sample preparation consisted of a protein precipitation extraction followed by derivatization with 10 M hydrochloric acid–methanol (10:90, v/v) and determined by liquid chromatography coupled with tandem mass spectrometry. The selected reaction monitoring mode of the positive ion was performed and the precursor to the product ion transitions of m/z 343→284 and m/z 299→152 were used to measure the derivative of peramivir and Ro 64-0802 (internal standard, an active metabolite of oseltamivir). The chromatographic separation was achieved using a ZORBAX RX-C8 (2.0 mm×150 mm×5 μm) analytical column with an isocratic mobile phase composed of acetonitrile–water–formic acid (30:70:0.1, v/v/v, 0.2 mL/min). The method was linear over a concentration range of 0.25–250 ng/mL. The average intra-day/inter-day precision values were 4.04–8.17% and 3.02–7.08%, respectively, while the average accuracy value was 93.99–106.48%. This method has been successfully applied to the preclinical dog research of peramivir following intragastric administration.
机译:Peramivir是一种用于抗流感的新型流感神经氨酸酶抑制剂。在本文中,开发了一种新颖的方法,可通过衍生化处理步骤确定狗血浆中的帕拉米韦,以增加保留时间并增强信号强度。样品制备包括蛋白质沉淀提取,然后用10 M盐酸-甲醇(10:90,v / v)衍生化,并通过液相色谱和串联质谱法测定。进行选定的正离子反应监测模式,并使用m / z 343→284和m / z 299→152的产物离子跃迁的前体来测量peramivir和Ro 64-0802(内标,奥司他韦的活性代谢产物)。使用ZORBAX RX-C8(2.0 mm×150 mm×5μm)分析柱进行色谱分离,该色谱柱的等度流动相为乙腈-水-甲酸(30:70:0.1,v / v / v,0.2 mL / min)。该方法在0.25–250 ng / mL的浓度范围内是线性的。日内/日间平均精度值分别为4.04–8.17%和3.02–7.08%,而平均精度值为93.99–106.48%。该方法已成功应用于peramivir胃内给药后的临床前狗研究。

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