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在涂覆有PAMAPTAC的毛细管中进行的逆流电泳中抗癫痫药物的大体积样品堆积。

Large volume sample stacking of antiepileptic drugs in counter current electrophoresis performed in PAMAPTAC coated capillary.

作者信息

Tůma Petr, Hložek Tomáš, Sommerová Blanka, Koval Dušan

机构信息

Department of Hygiene, Third Faculty of Medicine, Charles University, Ruská 87, 100 00, Prague 10, Czech Republic.

Department of Hygiene, Third Faculty of Medicine, Charles University, Ruská 87, 100 00, Prague 10, Czech Republic; Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 532 10, Pardubice, Czech Republic.

出版信息

Talanta. 2021 Jan 1;221:121626. doi: 10.1016/j.talanta.2020.121626. Epub 2020 Sep 8.

Abstract

Electrophoretic stacking is developed for sensitive determination of three zwitterionic antiepileptics, namely vigabatrin, pregabalin and gabapentin, in human serum. CE separation is performed in a 25 μm fused silica capillary covalently coated with the copolymer of acrylamide with 5% content of permanently charged 3-acrylamidopropyl trimethylammonium chloride (PAMAPTAC). In background electrolyte of 500 mM acetic acid, the 5% PAMAPTAC generates an anodic electro-osmotic flow with a magnitude of (-18.6 ± 0.5) · 10 mVs, which acts against the direction of the electrophoretic migration of the analytes. A sample of the antiepileptic prepared in a 25% v/v infusion solution and 75% v/v acetonitrile is injected into the capillary in a large volume attaining a zone length of up to 270 mm. After turning on the separation voltage, the antiepileptics are isotachophoretically focussed behind the zone of Na ions with a sensitivity enhancement factor of 78. For the clinical determination of antiepileptics, the human serum is diluted with acetonitrile in a ratio of 1:3 v/v and a zone with a length of 90 mm is injected into the capillary. The method is linear in the 0.025-2.5 μg/mL concentration range; the attained limit of quantification is in the range 18.3-22.8 nmol/L; the within-day precision for the migration time is 0.8-1.2% and for the peak area 1.5-2.4%.

摘要

开发了一种电泳堆积方法,用于灵敏测定人血清中的三种两性离子抗癫痫药物,即氨己烯酸、普瑞巴林和加巴喷丁。采用内径为25μm的熔融石英毛细管进行毛细管电泳分离,该毛细管共价涂覆有丙烯酰胺与5%含量的永久带电的3-丙烯酰胺基丙基三甲基氯化铵(PAMAPTAC)的共聚物。在500mM乙酸的背景电解质中,5%的PAMAPTAC产生大小为(-18.6±0.5)·10 mVs的阳极电渗流,其作用方向与分析物的电泳迁移方向相反。将在25% v/v输注溶液和75% v/v乙腈中制备的抗癫痫药物样品大量注入毛细管,获得的区带长度可达270mm。开启分离电压后,抗癫痫药物在钠离子区带后等速聚焦,灵敏度增强因子为78。对于抗癫痫药物的临床测定,将人血清与乙腈按1:3 v/v的比例稀释,并将长度为90mm的区带注入毛细管。该方法在0.025-2.5μg/mL浓度范围内呈线性;达到的定量限在18.3-22.8nmol/L范围内;迁移时间的日内精密度为0.8-1.2%,峰面积的日内精密度为1.5-2.4%。

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