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高效液相色谱法与固相萃取法用于N1,N3-双-(五氟苄基)-N7-(2-[五氟苄氧基]乙基)黄嘌呤(一种源自环氧乙烷DNA加合物的产物)气相色谱-电子捕获负离子质谱分析前衍生化后净化的比较

High-performance liquid chromatography versus solid-phase extraction for post-derivatization cleanup prior to gas chromatography-electron-capture negative-ion mass spectrometry of N1,N3-bis-(pentafluorobenzyl)-N7- (2-[pentafluorobenzyloxy]ethyl)xanthine, a product derived from an ethylene oxide DNA adduct.

作者信息

Saha M, Giese R W

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, Northeastern University, Boston, MA 02115.

出版信息

J Chromatogr. 1993 Jan 15;629(1):35-40. doi: 10.1016/0021-9673(93)80351-8.

Abstract

N7-(2-Hydroxyethyl)xanthine (N7-HEX), as a standard, has been measured at the low picomole level by the following sequence of steps: (1) derivatization with pentafluorobenzyl bromide; (2) post-derivatization sample cleanup by reversed-phase high-performance liquid chromatography (HPLC) or silica solid-phase extraction; and (3) separation/detection by gas chromatography electron-capture negative-ion mass spectrometry (GC-ECNI-MS). The average yield of product from the two sample cleanup procedures applied to 95 pg (0.48 pmol) of N7-HEX was comparable: 60% for HPLC; 56% for solid-phase extraction. The reaction blanks (0 pg N7-HEX) showed an interfering GC-ECNI-MS peak after HPLC cleanup. This problem was not encountered with solid-phase extraction, which, along with its greater convenience, made it the preferred technique for post-derivatization sample cleanup.

摘要

作为标准品的N7-(2-羟乙基)黄嘌呤(N7-HEX),已通过以下步骤序列在低皮摩尔水平进行了测定:(1)用五氟苄基溴进行衍生化;(2)通过反相高效液相色谱(HPLC)或硅胶固相萃取对衍生化后的样品进行净化;(3)通过气相色谱电子捕获负离子质谱(GC-ECNI-MS)进行分离/检测。应用于95皮克(0.48皮摩尔)N7-HEX的两种样品净化程序的产物平均产率相当:HPLC为60%;固相萃取为56%。反应空白(0皮克N7-HEX)在HPLC净化后显示出一个干扰性的GC-ECNI-MS峰。固相萃取未遇到此问题,并且其更具便利性,使其成为衍生化后样品净化的首选技术。

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