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大鼠和猴子体内α-甲基芴-2-乙酸(环丙洛芬)光学构型的转化

Inversion of optical configuration of alpha-methylfluorene-2-acetic acid (cicloprofen) in rats and monkeys.

作者信息

Lan S J, Kripalani K J, Dean A V, Egli P, Difazio L T, Schreiber E C

出版信息

Drug Metab Dispos. 1976 Jul-Aug;4(4):330-9.

PMID:8287
Abstract

A simple and sensitive radiometric method to determine the individual enantiomers of cicloprofen has been developed. 14C-Cicloprofen was converted to its L-leucine diastereoisomers, which were separated by thin-layer chromatography and quantified by measuring the radioactivity in the area corresponding to each individual diastereoisomer. This technique has also been used to measure the enantiomers of unlabeled cicloprofen by condensing with 14C-labeled L-leucine. By using the radiometric method, a unique biotransformation process, the inversion of the (-)-enantiomer of alpha-methylfluorene-2-acetic acid to its (+)-enantiomer, has been demonstrated in the rat and monkey. The rate of (-)- to (+)-inversion was found to be faster in the rat than in the monkey. After single or repeated oral adminstration of the racemic modification or the (-)-enantiomer of cicloprofen to both species, the ratio of (+)- to (-)-enantiomers of cicloprofen in plasma, urine, or bile increased with time. At 5, 22, and 48 hr after oral administration of a single 50-mg/kg dose of the (-)-enantiomer, 14C-cicloprofen in rat plasma contained 20, 50, and 79%, respectively, of the (+)-enantiomer. After receiving the same dose of (-)-enantiomer, monkey plasma contained 16.5% and 32% of (+)-enantiomer at 8 and 24 hr, respectively. After oral administration of a single 50-mg/kg dose of the (+)-enantiomer of 14C-cicloprofen to rats and monkeys, the percentage of (-)-enantiomer in plasma varied from 2 to 15%. Since the administered (+)-enantiomer contained 4% of (-)-enantiomer and the (+)-enantiomer was excreted at a faster rate than its (-)-antipode by rats or monkeys, it is not known whether an occasional small percentage increase of (-)-enantiomer in plasma resulted from the (+)-to-(-) inversion, or from faster elimination of the (+)-enantiomer. Nevertheless, if (+)-to-(-) inversion does occur in these two species, the rate is much slower than for the (-)-to-(+) inversion.

摘要

已开发出一种简单且灵敏的放射性测定法来测定环丙洛芬的各个对映体。将14C - 环丙洛芬转化为其L - 亮氨酸非对映异构体,通过薄层色谱法分离,并通过测量与每个单独非对映异构体相对应区域的放射性进行定量。该技术还用于通过与14C标记的L - 亮氨酸缩合来测量未标记环丙洛芬的对映体。通过使用放射性测定法,在大鼠和猴子中已证明了一种独特的生物转化过程,即α - 甲基芴 - 2 - 乙酸的( - ) - 对映体转化为其( + ) - 对映体。发现大鼠中( - ) - 向( + ) - 转化的速率比猴子快。对这两个物种单次或重复口服消旋体或环丙洛芬的( - ) - 对映体后,血浆、尿液或胆汁中环丙洛芬的( + ) - 与( - ) - 对映体的比例随时间增加。在单次口服50mg/kg剂量的( - ) - 对映体后5、22和48小时,大鼠血浆中的14C - 环丙洛芬分别含有20%、50%和79%的( + ) - 对映体。接受相同剂量的( - ) - 对映体后,猴子血浆在8和24小时分别含有16.5%和32%的( + ) - 对映体。给大鼠和猴子单次口服50mg/kg剂量的14C - 环丙洛芬的( + ) - 对映体后,血浆中( - ) - 对映体的百分比在2%至15%之间变化。由于所给予的( + ) - 对映体含有4%的( - ) - 对映体,并且大鼠或猴子中( + ) - 对映体的排泄速度比其( - ) - 对映体快,所以尚不清楚血浆中( - ) - 对映体偶尔出现的小百分比增加是由于( + ) - 向( - ) - 转化,还是由于( + ) - 对映体的更快消除。然而,如果在这两个物种中确实发生了( + ) - 向( - ) - 转化,其速率比( - ) - 向( + ) - 转化慢得多。

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