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Field-Amplified on-line Sample Stacking for Separation and Determination of Adefovir and Tenofovir Using Capillary Electrophoresis

机译:现场扩增在线样品堆叠,用于使用毛细管电泳分离和测定阿德福韦和替诺福韦

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摘要

An on-line sample stacking method known as field amplified sample stacking, using hydroxypropylmethyl cellulose as electro-osmotic flow suppressant, was developed for separation and identification of adefovir and tenofovir for the first time. A water plug (hydrodynamic injection for 15 s. 2.0 psi) was added to the system prior to the loading of sample (electrokinetic injection at cathode end (14.6 kV, 20 s)) in the capillary (80 cm x 75 μm). The separation was performed using phosphate solution containing 0.3 % hydroxypropylmethyl cellulose and measured at 18 kV and 214 nm. Comparing with the conventional capillary electrophoresis, the signal enhancement factor was found to be 146 for adefovir (LOD = 2.67 ng mL~(-1)) and 137 for tenofovir (LOD = 3.22 ng mL~(-1)) (S/N = 3). The proposed method has potential application in pharmacokinetics and can reach detection limits comparable to mass spectrometry, a more complicated and costly procedures.
机译:为了首次分离和鉴定阿德福韦和替诺福韦,开发了一种使用羟丙基甲基纤维素作为电渗流抑制剂的在线样品堆积方法,称为现场扩增样品堆积。在将样品加载到毛细管(80 cm x 75μm)中之前(在阴极端(14.6 kV,20 s)进行电动注入)之前,向系统中添加了一个水塞(15 s。2.0 psi的流体动力注入)。使用含有0.3%羟丙基甲基纤维素的磷酸盐溶液进行分离,并在18kV和214nm下测量。与常规毛细管电泳相比,阿德福韦(LOD = 2.67 ng mL〜(-1))的信号增强因子为146,替诺福韦(LOD = 3.22 ng mL〜(-1))的信号增强因子为137(S / N = 3)。所提出的方法在药代动力学中具有潜在的应用前景,并且可以达到与质谱相当的检测极限,这是一个更复杂,成本更高的程序。

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