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新型双荧光和电化学检测器用于邻苯二甲醛-二茂铁/6-二茂铁基-1-己硫醇柱前衍生化高效液相色谱法测定二甲基精氨酸

The stable o-phthalaldehyde-ferrocene/6-ferrocenyl-1-hexanethiol pre-column derivatization high-performance liquid chromatography of dimethylarginine by novel dual fluorescence and electrochemical detector.

作者信息

Suzuki Katsuhiro, Katayama Masatoki, Takamatsu Kiyoshi, Kaneko Satoru, Ishikawa Hiromichi, Tsukimura Takahiro, Togawa Tadayasu

机构信息

Drug Metabolism Research Laboratories, Drug Discovery Research, Astellas Pharma Inc., Kashima, Yodogawa-ku, Osaka, Japan.

出版信息

Biomed Chromatogr. 2013 Apr;27(4):535-8. doi: 10.1002/bmc.2823. Epub 2012 Sep 28.

Abstract

Monomethylarginine, asymmetric dimethylarginine and symmetric dimethylarginine were separated on a Wakopak Combi ODS with an acetonitrile-100 mm potassium phosphate buffer (pH 7.0; 1:1, v/v). Dimethylarginines were derived from o-phthalaldehyde for the fluorescence detector and from 6-ferrocenyl-1-hexanethiol for the electrochemical detector. The detection limits of the dimethylarginines in spiked plasma were 0.3-0.5 pmol by electrochemical detection and 1-2 pmol by fluorescence detection. The detection limits were improved over 30 times by electrochemical detection and 10 times by fluorescence detection compared with previous reports. In previous derivatization liquid chromatography, the reaction solutions, o-phthalaldehyde, 2-mercaptethanol and dimethylarginines were unstable and required quick derivatization at 4°C. By our proposed pre-column methods, the dimethylarginines were derivatized at room temperature and the fluorescent products were stable for 6 h. The manipulation performance was greatly advanced compared with previous LC reports. This is the first report on stable and sensitive dimethylarginines by dual detection. The selectivity was also improved by dual detection. The proposed method was applied to preliminary monitoring of dimethylargines in plasma and urine.

摘要

在Wakopak Combi ODS柱上,使用乙腈 - 100 mM磷酸钾缓冲液(pH 7.0;1:1,v/v)对单甲基精氨酸、不对称二甲基精氨酸和对称二甲基精氨酸进行分离。二甲基精氨酸分别用邻苯二甲醛衍生用于荧光检测器,用6 - 二茂铁基 - 1 - 己硫醇衍生用于电化学检测器。加标血浆中二甲基精氨酸的检测限,电化学检测为0.3 - 0.5 pmol,荧光检测为1 - 2 pmol。与之前的报道相比,电化学检测的检测限提高了30倍以上,荧光检测提高了10倍。在之前的衍生化液相色谱中,反应溶液、邻苯二甲醛、2 - 巯基乙醇和二甲基精氨酸不稳定,需要在4°C下快速衍生化。通过我们提出的柱前方法,二甲基精氨酸在室温下衍生化,荧光产物稳定6小时。与之前的液相色谱报道相比,操作性能有了很大提高。这是关于通过双重检测实现稳定且灵敏的二甲基精氨酸的首次报道。双重检测还提高了选择性。所提出的方法应用于血浆和尿液中二甲基精氨酸的初步监测。

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