Suppr超能文献

采用改良的大鼠原位吸收法研究非马沙坦在胃肠道的局部吸收情况。

Regional Absorption of Fimasartan in the Gastrointestinal Tract by an Improved in situ Absorption Method in Rats.

作者信息

Kim Tae Hwan, Paik Soo Heui, Chi Yong Ha, Bulitta Jürgen B, Lee Da Young, Lim Jun Young, Chung Seung Eun, Song Chang Ho, Jeong Hyeon Myeong, Shin Soyoung, Shin Beom Soo

机构信息

College of Pharmacy, Catholic University of Daegu, Gyeongsan, Gyeongbuk 38430 Korea.

College of Pharmacy, Sunchon National University, Sunchon, Jeonnam 57992, Korea.

出版信息

Pharmaceutics. 2018 Oct 3;10(4):174. doi: 10.3390/pharmaceutics10040174.

Abstract

The aim of the present study was to assess the regional absorption of fimasartan by an improved in situ absorption method in comparison with the conventional in situ single-pass perfusion method in rats. After each gastrointestinal segment of interest was identified, fimasartan was injected into the starting point of each segment and the unabsorbed fimasartan was discharged from the end point of the segment. Blood samples were collected from the jugular vein to evaluate the systemic absorption of the drug. The relative fraction absorbed () values in the specific gastrointestinal region calculated based on the area under the curve (AUC) values obtained after the injection of fimasartan into the gastrointestinal segment were 8.2% ± 3.2%, 23.0% ± 12.1%, 49.7% ± 11.5%, and 19.1% ± 11.9% for the stomach, duodenum, small intestine, and large intestine, respectively, which were comparable with those determined by the conventional in situ single-pass perfusion. By applying the fraction of the dose available at each gastrointestinal segment following the oral administration, the actual fraction absorbed () values at each gastrointestinal segment were estimated at 10.9% for the stomach, 27.1% for the duodenum, 40.7% for the small intestine, and 5.4% for the large intestine, which added up to the gastrointestinal bioavailability () of 84.1%. The present method holds great promise to assess the regional absorption of a drug and aid to design new drug formulations.

摘要

本研究的目的是通过改进的原位吸收方法,与传统的大鼠原位单通道灌注方法相比,评估非马沙坦的区域吸收情况。在确定每个感兴趣的胃肠道段后,将非马沙坦注入每个段的起点,并将未吸收的非马沙坦从段的终点排出。从颈静脉采集血样以评估药物的全身吸收情况。基于将非马沙坦注入胃肠道段后获得的曲线下面积(AUC)值计算的特定胃肠道区域的相对吸收分数()值,胃、十二指肠、小肠和大肠分别为8.2%±3.2%、23.0%±12.1%、49.7%±11.5%和19.1%±11.9%,与传统原位单通道灌注法测定的值相当。通过应用口服给药后每个胃肠道段可用剂量的分数,估计每个胃肠道段的实际吸收分数()值,胃为10.9%,十二指肠为27.1%,小肠为40.7%,大肠为5.4%,它们加起来的胃肠道生物利用度()为84.1%。本方法在评估药物的区域吸收和辅助设计新药物制剂方面具有很大的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de9f/6320822/0e4a69fb65ed/pharmaceutics-10-00174-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验