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使用邻苯二甲醛和3-巯基丙酸进行柱前衍生化后,采用高效液相色谱法测定生物样品中的d-苯丙胺。

Determination of d-amphetamine in biological samples using high-performance liquid chromatography after precolumn derivatization with o-phthaldialdehyde and 3-mercaptopropionic acid.

作者信息

Bowyer J F, Clausing P, Newport G D

机构信息

Division of Neurotoxicology, National Center for Toxicological Research, Jefferson, AR 72079-9502, USA.

出版信息

J Chromatogr B Biomed Appl. 1995 Apr 21;666(2):241-50. doi: 10.1016/0378-4347(94)00573-n.

Abstract

An HPLC method is described for the determination of amphetamine using fluorometric detection after derivatization with o-phthaldialdehyde and 3-mercaptopropionic acid. This procedure is more sensitive (detection limit 370 fmol in microdialysate buffer standards, 1.5 pmol in extracted plasma and tissue samples) than most of the previous methods described for the determination of amphetamine with HPLC-fluorescence detection. Due to the stability of the derivative it is also suitable for autosampling after manual derivatization. Investigators currently using o-phthaldialdehyde derivatization and fluorometric detection for amino acid determination should be able to rapidly implement this method.

摘要

本文描述了一种高效液相色谱(HPLC)方法,用于测定苯丙胺。该方法是在苯丙胺与邻苯二甲醛和3-巯基丙酸衍生化后,采用荧光检测。与大多数先前描述的用HPLC-荧光检测法测定苯丙胺的方法相比,本方法更为灵敏(在微透析缓冲液标准品中的检测限为370飞摩尔,在提取的血浆和组织样品中的检测限为1.5皮摩尔)。由于衍生物的稳定性,它也适用于手动衍生化后的自动进样。目前使用邻苯二甲醛衍生化和荧光检测法测定氨基酸的研究人员应该能够快速采用此方法。

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