Azmin M N, Stuart J F, Florence A T
Cancer Chemother Pharmacol. 1985;14(3):238-42. doi: 10.1007/BF00258124.
This paper describes further exploration of the effect of polysorbate 80 on the absorption, distribution, and elimination of methotrexate (MTX). This study has confirmed the earlier finding that polysorbate 80 could increase the absorption of MTX from the mouse gastrointestinal tract and enhance the drugs uptake into the brain. The experiments reported here suggest that polysorbate 80 has a direct effect on the blood-brain barrier leading to the increased uptake of MTX, which is evident following IV administration. Measurements of MTX excreted in the urine and faeces confirmed the role of polysorbate 80 in facilitating the excretion of MTX into the bile and urine. Polysorbate 80 administered PO did not cause any reduction of plasma volume, thus excluding the possibility that the higher MTX concentrations measured in mice after concurrent administration of polysorbate PO might result from a reduction in blood volume due to osmotic effects. At the doses given, polysorbate 80 appeared not to have a damaging effect on the gastrointestinal mucosa.
本文描述了对聚山梨酯80对甲氨蝶呤(MTX)吸收、分布和消除影响的进一步探索。本研究证实了先前的发现,即聚山梨酯80可增加MTX从小鼠胃肠道的吸收,并增强药物进入大脑的摄取。此处报道的实验表明,聚山梨酯80对血脑屏障有直接作用,导致MTX摄取增加,静脉给药后这一现象很明显。对尿液和粪便中排出的MTX的测量证实了聚山梨酯80在促进MTX排泄到胆汁和尿液中的作用。口服聚山梨酯80不会导致血浆量减少,因此排除了同时口服聚山梨酯后小鼠体内测得的较高MTX浓度可能是由于渗透作用导致血容量减少所致的可能性。在给定剂量下,聚山梨酯80似乎对胃肠道黏膜没有损害作用。