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首页> 外文期刊>Biological & pharmaceutical bulletin >Stomach- and site-selective delivery of 5-fluorouracil following its application on the gastric serosal surface in rats.
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Stomach- and site-selective delivery of 5-fluorouracil following its application on the gastric serosal surface in rats.

机译:5-氟尿嘧啶在大鼠胃浆膜表面上的胃和部位选择性递送。

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摘要

The present study was undertaken to elucidate the stomach- and site-selective delivery of 5-fluorouracil (5-FU) following its application on the gastric serosal surface in rats. An experimental system utilizing a cylindrical diffusion cell attached to the gastric serosal surface was established. To evaluate the gastric distribution of 5-FU, the stomach was separated into the site under the diffusion cell (site 1) and the site not under the diffusion cell (site 2). Furthermore, the mucosal side at site 1 was separated from the serosal side. After intravenous and oral administration of 5-FU, the 5-FU concentrations at sites 1 and 2 until 240 min were similar. After gastric serosal surface application of 5-FU, however, the concentration of 5-FU at site 1 until 240 min was approximately 10-fold higher than that at site 2, and was sustained. Furthermore, the 5-FU concentration on the mucosal side at site 1 and the serosal side at site 1 were comparable after gastric serosal surface application. The blood concentration of 5-FU was low (<4.4 microg/ml) until 240 min after gastric serosal surface application. The maximum blood concentration of 5-FU after gastric serosal surface application was significantly lower than after intravenous administration. Thus, the stomach- and site-selective delivery system following application on the gastric serosal surface could be applied with anticancer drugs for the treatment of gastric cancer.
机译:进行本研究以阐明5-氟尿嘧啶(5-FU)在大鼠胃浆膜表面的应用后在胃和部位的选择性递送。建立了利用附着在胃浆膜表面的圆柱形扩散池的实验系统。为了评估5-FU在胃中的分布,将胃分为扩散池下方的部位(部位1)和不在扩散池下方的部位(部位2)。此外,部位1处的粘膜侧与浆膜侧分离。静脉内和口服施用5-FU后,直到240分钟,部位1和2处的5-FU浓度相似。然而,在胃浆膜表面应用5-FU后,直到240分钟,部位1处的5-FU浓度比部位2处的浓度高约10倍,并且持续存在。此外,在应用胃浆膜表面后,部位1的粘膜侧和部位1的浆膜侧的5-FU浓度相当。 5-FU的血药浓度一直很低(<4.4 microg / ml),直到应用胃浆膜表面后240分钟为止。胃浆膜表面施用后5-FU的最大血药浓度明显低于静脉内施用后。因此,在胃浆膜表面上施用后的胃和部位选择性递送系统可以与抗癌药一起用于治疗胃癌。

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