地高辛在大鼠体内的鼻腔吸收。

Y Kato, N Yagi, S Yamada, M Sato, R Kimura
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引用次数: 3

摘要

对大鼠鼻给药地高辛进行了研究,并与静脉、十二指肠和直肠给药进行了比较。结果表明,经鼻给药后血浆地高辛水平与静脉给药后相当。经十二指肠和直肠给药可显著降低血浆水平。这些数据表明地高辛通过鼻膜吸收是一种合理的方法。在原位鼻腔和肠道灌注实验中,地高辛从灌注液中消失,遵循明显的一级动力学。地高辛的鼻腔和肠道吸收率随着灌注量的增加而降低。吸收速率常数与1/容积的关系呈直线,表明地高辛是通过被动扩散过程从鼻黏膜吸收的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nasal absorption of digoxin in rats.

The nasal administration of digoxin was studied in rats and compared to intravenous, intraduodenal and rectal administration of the drug. The results indicated that the plasma level of digoxin after nasal administration was comparable to the level after intravenous injection. Administration by the intraduodenal and rectal routes resulted in considerably lower plasma levels. These data reveal that digoxin absorption across the nasal membranes is a reasonable approach. In the in situ nasal and intestinal perfusion experiments, digoxin disappeared from the perfusate following the apparent first-order kinetics. The nasal and intestinal absorption rate of digoxin was reduced by an increase in the perfusion volume. The plot of absorption rate constant against 1/volume resulted in a straight line, suggesting that digoxin is absorbed from nasal mucosa by a passive diffusion process.

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