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N-乙酰基-(1-氨基-2-萘酚-6-磺酸),日落黄FCF、橙GGN和1-氨基-2-萘酚-6-磺酸在大鼠尿液中的常见代谢产物。

N-acetyl-(1-amino-2-naphthol-6-sulphonic acid), a common metabolite of sunset yellow FCF, orange GGN and 1-amino-2-naphthol-6-sulphonic acid in rat urine.

作者信息

De Beer J O, Dierickx P J, Grimée R I

出版信息

J Chromatogr. 1982 Mar 5;237(1):115-25. doi: 10.1016/s0021-9673(00)88278-3.

Abstract

Sunset Yellow FCF, Orange GGN and 1-amino-2-naphthol-6-sulphonic acid (ANSA) were administered to male Wistar rats by stomach intubation. Aromatic sulphonic acids excreted in 24-h urines after enzymatic cleavage of the azo link in the dyes were isolated using a thoroughly elaborated ion-pair extraction method and further separated by means of a reversed-phase ion-pair liquid chromatographic system. Blank 24-h rat urines were extracted and run at the same time under identical analytical circumstances. In addition to the peaks corresponding to sulphanilic and metanilic acid and their N-acetylated derivatives, which are metabolites arising from Sunset Yellow FCF and Orange GGN, respectively, an important common peak appeared on the chromatograms, which was absent from the blank urine extracts. After analysis of 24-h urine of rats that had received ANSA, a peak with the same retention time as this unknown common peak could be detected under the same liquid chromatographic conditions, the retention time of which was different from that of the ANSA standard. However, after derivatization of the ANSA standard with acetic anhydride, followed by liquid chromatographic examination of the derivatised mixture, two peaks appeared on the chromatogram, the first of which had the same retention time and the same UV-spectrum as the unknown common peak in rat urine extracts. By means of semi-preparative liquid chromatographic separation and isolation, followed by further purification over a cation-exchange resin, the compound corresponding to the unknown common peak could be identified by FT-PMR spectroscopy as N-acetyl-ANSA.

摘要

通过胃插管法给雄性Wistar大鼠施用日落黄FCF、橙GGN和1-氨基-2-萘酚-6-磺酸(ANSA)。采用精心设计的离子对萃取法分离经酶解染料中偶氮键后在24小时尿液中排泄的芳香族磺酸,并通过反相离子对液相色谱系统进一步分离。同时在相同分析条件下对空白24小时大鼠尿液进行萃取和检测。除了分别对应于来自日落黄FCF和橙GGN代谢产物的对氨基苯磺酸和间氨基苯磺酸及其N-乙酰化衍生物的峰外,色谱图上还出现了一个重要的共同峰,而在空白尿液萃取物中没有该峰。在分析接受ANSA的大鼠的24小时尿液后,在相同液相色谱条件下可检测到一个与该未知共同峰保留时间相同的峰,其保留时间与ANSA标准品不同。然而,用乙酸酐将ANSA标准品衍生化后,对衍生化混合物进行液相色谱检测,色谱图上出现了两个峰,其中第一个峰的保留时间和紫外光谱与大鼠尿液萃取物中的未知共同峰相同。通过半制备液相色谱分离和纯化,再经阳离子交换树脂进一步纯化,利用傅里叶变换质子磁共振光谱法将对应于未知共同峰的化合物鉴定为N-乙酰-ANSA。

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