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环孢素代谢物的临床意义。

The clinical significance of cyclosporine metabolites.

作者信息

Yatscoff R W, Rosano T G, Bowers L D

机构信息

Department of Clinical Chemistry, Health Sciences Centre, Winnipeg, Manitoba, Canada.

出版信息

Clin Biochem. 1991 Feb;24(1):23-35. doi: 10.1016/0009-9120(91)90126-y.

Abstract

Cyclosporine (CsA) is extensively metabolized, with over 14 metabolites having been characterized to date. The confirmation of structure and purity is a prerequisite for studies involving CsA metabolites. Analytical techniques such as fast atom bombardment/mass spectroscopy (FAB/MS), tandem mass spectrometry (MS), 1H- and 13C-nuclear magnetic resonance (NMR) can be used for such purposes. In vitro experiments indicate that metabolites are considerably less immunosuppressive and toxic than CsA. In vivo studies have been hampered by sufficient quantities of metabolites and a suitable animal model. Preliminary results in the rat suggest that CsA metabolites are less immunosuppressive and toxic than CsA, although these results must be confirmed using a more suitable animal model. Present data indicate that the routine monitoring of metabolites is not warranted in transplant patients, although additional information is required to confirm these findings.

摘要

环孢素(CsA)具有广泛的代谢过程,迄今为止已鉴定出14种以上的代谢物。结构和纯度的确认是涉及CsA代谢物研究的先决条件。诸如快原子轰击/质谱(FAB/MS)、串联质谱(MS)、1H和13C核磁共振(NMR)等分析技术可用于此目的。体外实验表明,代谢物的免疫抑制和毒性比CsA小得多。体内研究因代谢物数量不足和缺乏合适的动物模型而受到阻碍。大鼠的初步结果表明,CsA代谢物的免疫抑制和毒性比CsA小,尽管这些结果必须使用更合适的动物模型来确认。目前的数据表明,尽管需要更多信息来证实这些发现,但移植患者中对代谢物进行常规监测并无必要。

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