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肠道中“未搅动”水层对口服给药后吸收速率和吸收程度的影响。

Effect of 'unstirred' water layer in the intestine on the rate and extent of absorption after oral administration.

作者信息

Chiou W L

机构信息

Department of Pharmaceutics and Pharmacodynamics, College of Pharmacy, University of Illinois at Chicago 60612.

出版信息

Biopharm Drug Dispos. 1994 Nov;15(8):709-17. doi: 10.1002/bdd.2510150808.

Abstract

The presence of an aqueous diffusion layer or 'unstirred' water layer adjacent to the intestinal membrane has long been regarded as a potential barrier for intestinal absorption of compounds. Theoretical analyses were performed in the present study to quantitatively determine the effect of this layer on the rate and extent of absorption of passively absorbed compounds with different membrane absorption half-lives (10 to 300 min) in humans, dogs, rabbits, rats and mice. Diffusion half-lives across this (40 microns thick) layer were estimated to be 5.8, 2.5, 1.1, 0.65 and 0.32 min, respectively, in the distended intestine of the above five species. These half-lives are reduced by about 5-fold when the intestine is about 80% 'flat' in fasting state. The results of extensive analysis indicate that the presence of such a layer is generally expected to have a relatively mild or insignificant effect on the rate of absorption and an insignificant effect on the extent of absorption. The study also indicates that an aqueous layer of 708 microns has practically no effect on the extent of absorption of progesterone, a highly lipophilic compound, in rats. For prediction of or correlation with the fraction of oral dose absorbed after oral administration, the present study indicates that use of apparent or effective permeability rather than unbiased or true wall (membrane) permeability, as advocated earlier by others, should generally suffice.

摘要

长期以来,人们一直认为在肠膜附近存在水扩散层或“未搅动”水层是化合物肠道吸收的潜在障碍。本研究进行了理论分析,以定量确定该层对人类、狗、兔子、大鼠和小鼠中具有不同膜吸收半衰期(10至300分钟)的被动吸收化合物的吸收速率和程度的影响。在上述五个物种的扩张肠道中,穿过该(40微米厚)层的扩散半衰期估计分别为5.8、2.5、1.1、0.65和0.32分钟。当肠道在禁食状态下约80%“扁平”时,这些半衰期会减少约5倍。广泛分析的结果表明,通常预计这样一层的存在对吸收速率的影响相对较小或不显著,对吸收程度的影响不显著。该研究还表明,708微米的水层对大鼠中高度亲脂性化合物孕酮的吸收程度实际上没有影响。对于口服给药后吸收的口服剂量分数的预测或相关性,本研究表明,使用表观或有效渗透率而不是其他人先前主张的无偏或真实壁(膜)渗透率通常就足够了。

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