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大鼠体内单氟代抗精神病药物的¹⁹F核磁共振研究

In vivo 19F nuclear magnetic resonance of a monofluorinated neuroleptic in the rat.

作者信息

Günther U, Albert K

机构信息

Institut für Organische Chemie der Universität, Tübingen, Germany.

出版信息

NMR Biomed. 1993 Jan-Feb;6(1):27-31. doi: 10.1002/nbm.1940060105.

Abstract

In vivo 19F NMR measurements of the fluorinated neuroleptic melperone [4'-fluoro-4-(4-methylpiperidino)-butyrophenone hydrochloride] in the rat brain were performed using a geometrically optimized surface coil at 4.7 T. It was possible for the first time to detect a signal of a monofluorinated neuroleptic drug with a time resolution of 30 min after i.p. application. The kinetic time course of the investigated neuroleptic melperone was recorded over 6 h and showed that the half-life in the rat brain is 4.3 h. The total amount of drug and its metabolites in the brain was estimated to be 50 microM. the chemical shift of the 19F NMR signal shows the same upfield shift relative to that in aqueous solution as has been reported for trifluorinated neuroleptic drugs.

摘要

在4.7T磁场下,使用几何优化表面线圈对大鼠脑中的氟化抗精神病药物美哌隆[4'-氟-4-(4-甲基哌啶基)-丁酰苯盐酸盐]进行了体内19F NMR测量。首次能够在腹腔注射后30分钟的时间分辨率下检测到单氟抗精神病药物的信号。对所研究的抗精神病药物美哌隆的动力学时间进程进行了6小时的记录,结果表明其在大鼠脑中的半衰期为4.3小时。脑中药物及其代谢物的总量估计为50微摩尔。19F NMR信号的化学位移相对于水溶液中的化学位移显示出相同的高场位移,这与三氟抗精神病药物的报道一致。

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