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大鼠口服给药后聚苯乙烯微球从胃肠道向循环系统的转移。

The transfer of polystyrene microspheres from the gastrointestinal tract to the circulation after oral administration in the rat.

作者信息

Eyles J, Alpar O, Field W N, Lewis D A, Keswick M

机构信息

Pharmaceutical Sciences Institute, Aston University, Birmingham, UK.

出版信息

J Pharm Pharmacol. 1995 Jul;47(7):561-5. doi: 10.1111/j.2042-7158.1995.tb06714.x.

Abstract

Factors relating to the transfer of latex microspheres of 0.87 micron mean diameter from the gastrointestinal tract (GIT) to the circulation have been investigated. The rapidity of appearance and the number of particles increased when the volume of water used as a suspending vehicle was increased. This was probably due to barrier cell integrity being compromised so that the movement of particles across the enterocytes would be enhanced. Particles were swept into these channels by the waterflow. The tonicity of the fluid was important as isotonic and hypertonic saline were not as effective as water in transferring particles. Particles were transferred from GIT segments adjacent to the stomach which may in part explain the rapid appearance of particles in the circulation. Particle uptake was blocked by cytochalasin B which suggests an active component may also be involved.

摘要

已对与平均直径为0.87微米的乳胶微球从胃肠道(GIT)转移至循环系统相关的因素进行了研究。当用作悬浮媒介的水量增加时,微球出现的速度和数量会增加。这可能是由于屏障细胞的完整性受到损害,从而增强了微粒穿过肠上皮细胞的移动。微粒被水流冲进这些通道。液体的张力很重要,因为等渗和高渗盐水在微粒转移方面不如水有效。微粒从紧邻胃部的胃肠道段转移,这可能部分解释了微粒在循环系统中迅速出现的原因。细胞松弛素B可阻断微粒摄取,这表明可能还涉及一个活跃成分。

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