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[二甲基亚砜对卡那霉素在腹膜内沉积的影响]

[Kanamycin deposition in the peritoneum as affected by dimexide].

作者信息

Zverev V M, Aleksevich Ia I, Rybas' A S, Khomitskiĭ N V

出版信息

Antibiotiki. 1981 Feb;26(2):102-4.

PMID:7212688
Abstract

The effect of dimexid (dimethylsulfoxide) on kanamycin absorption from the peritoneum was studied on normal albino rats with aseptic peritonitis. Contrary to the present opinion that the rate of various drug absorption into the blood increases under the effect of dimexid, it was shown that intraperitoneal administration of dimexid and kanamycin resulted in deposition of kanamycin in the peritoneum followed by its slow liberation into the blood channel. The concentration of kanamycin in the peritoneum increased 3--8 times under the effect of dimexid, thus prolonging its retention time by 10--13 hours. The depositing effect was more pronounced in the animals with peritonitis.

摘要

在患有无菌性腹膜炎的正常白化大鼠身上研究了二甲亚砜(Dimexid)对卡那霉素从腹膜吸收的影响。与目前认为在二甲亚砜作用下各种药物进入血液的速率会增加的观点相反,研究表明腹腔注射二甲亚砜和卡那霉素会导致卡那霉素在腹膜中沉积,随后缓慢释放到血液循环中。在二甲亚砜的作用下,腹膜中卡那霉素的浓度增加了3至8倍,从而使其保留时间延长了10至13小时。在患有腹膜炎的动物中,这种沉积作用更为明显。

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