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单次给予油酸钠后大鼠苯妥英血浆蛋白结合的长期损害

Prolonged impairment of the plasma-protein binding of phenytoin in the rat after a single dose of sodium oleate.

作者信息

Colburn W A, Gibaldi M

出版信息

Drug Metab Dispos. 1978 Jul-Aug;6(4):452-5.

PMID:28926
Abstract

The plasma-protein binding of phenytoin in rats was impaired for more than 14 days after a single injection of sodium oleate compared to that observed in saline-treated controls. A maximum free (unbound) phenytoin fraction value of about 0.30 was found between 30 and 120 min after oleate administration. The free fraction decreased to about 0.20 after 14 days. The free fraction of phenytoin in control rats was essentially constant over this period and averaged about 0.17. The impaired plasma-protein binding of phenytoin was unaffected by prolonged dialysis but was effectively reversed by charcoal treatment of the plasma. Comparison of the in vivo and in vitro effects of sodium oleate on phenytoin binding in plasma indicates that the reduction in binding is unrelated to the in vivo oleate concentration in plasma at the time of the binding determination. For example, 5 min after a bolus injection of oleate, the plasma free fraction of phenytoin was about 0.33. A comparable concentration of oleate in control plasma resulted in a free phenytoin fraction of only 0.21.

摘要

与生理盐水处理的对照组相比,大鼠单次注射油酸钠后,苯妥英的血浆蛋白结合受损超过14天。在给予油酸钠后30至120分钟之间,发现苯妥英的最大游离(未结合)分数值约为0.30。14天后,游离分数降至约0.20。在此期间,对照大鼠中苯妥英的游离分数基本恒定,平均约为0.17。苯妥英受损的血浆蛋白结合不受长时间透析的影响,但通过血浆的活性炭处理可有效逆转。油酸钠对血浆中苯妥英结合的体内和体外作用比较表明,结合的减少与结合测定时血浆中的体内油酸盐浓度无关。例如,快速注射油酸钠5分钟后,苯妥英的血浆游离分数约为0.33。对照血浆中相当浓度 的油酸钠导致游离苯妥英分数仅为0.21。

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