Ivanov Alexander Vladimirovich, Bulgakova Polina Olegovna, Virus Edward Danielevich, Kruglova Maria Petrovna, Alexandrin Valery Vasil'evich, Gadieva Viktoriya Aleksandrovna, Luzyanin Boris Petrovich, Kushlinskii Nikolai Evgen'evich, Fedoseev Anatolij Nikolaevich, Kubatiev Aslan Amirkhanovich
Federal State Budgetary Scientific Institution "Institute of General Pathology and Pathophysiology", Moscow, Russia.
Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation, Moscow, Russia.
Electrophoresis. 2017 Oct;38(20):2646-2653. doi: 10.1002/elps.201700133. Epub 2017 Aug 1.
A rapid and selective method has been developed for highly sensitive determination of total cysteine and homocysteine levels in human blood plasma and urine by capillary electrophoresis (CE) coupled with liquid-liquid extraction. Analytes were first derivatized with 1,1'-thiocarbonyldiimidazole and then samples were purified by chloroform-ACN extraction. Electrophoretic separation was performed using 0.1 M phosphate with 30 mM triethanolamine, pH 2, containing 25 μM CTAB, 2.5 μM SDS, and 2.5% polyethylene glycol 600. Samples were injected into the capillary (with total length 32 cm and 50 μm id) at 2250 mbar*s and subsequent injection was performed for 30 s with 0.5 M KОН. The total analysis time was less than 9 min, accuracy was 98%, and precision was <2.6%. The LOD was 0.2 μM for homocysteine and 0.5 μM for cysteine. The use of liquid-liquid extraction allowed the precision and sensitivity of the CE method to be significantly increased. The validated method was applied to determine total cysteine and homocysteine content in human blood plasma and urine samples obtained from healthy volunteers and patients with kidney disorders.
已开发出一种快速且选择性的方法,通过毛细管电泳(CE)结合液 - 液萃取来高灵敏度测定人血浆和尿液中的总半胱氨酸和同型半胱氨酸水平。分析物首先用1,1'-硫代羰基二咪唑衍生化,然后通过氯仿 - 乙腈萃取对样品进行纯化。使用含有25μM十六烷基三甲基溴化铵(CTAB)、2.5μM十二烷基硫酸钠(SDS)和2.5%聚乙二醇600的0.1M磷酸盐与30mM三乙醇胺(pH 2)进行电泳分离。在2250毫巴·秒的压力下将样品注入毛细管(总长度32厘米,内径50μm),随后用0.5M氢氧化钾进行30秒的进样。总分析时间少于9分钟,准确度为98%,精密度<2.6%。同型半胱氨酸的检测限为0.2μM,半胱氨酸的检测限为0.5μM。液 - 液萃取的使用显著提高了CE方法的精密度和灵敏度。该经过验证的方法用于测定从健康志愿者和肾脏疾病患者获得的人血浆和尿液样品中的总半胱氨酸和同型半胱氨酸含量。