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首页> 外文期刊>European journal of pharmaceutical sciences >Site of drug absorption after oral administration: Assessment of membrane permeability and luminal concentration of drugs in each segment of gastrointestinal tract.
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Site of drug absorption after oral administration: Assessment of membrane permeability and luminal concentration of drugs in each segment of gastrointestinal tract.

机译:口服后药物吸收的部位:评估胃肠道各部分中药物的膜通透性和腔内浓度。

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This study was conducted to assess the site of drug absorption in the gastrointestinal (GI) tract after oral administration. Drug permeability to different regions of rat intestine, jejunum, ileum and colon, was measured by in situ single-pass perfusion method. It was revealed that the epithelial surface area should not be a determinant of the regional difference in the intestinal permeability of highly permeable drugs. Effects of the mucus layer at the surface of the epithelium and the fluidity of the epithelial cell membrane on the drug permeability were investigated. These factors are demonstrated to contribute to the regional differences in intestinal drug permeability. The luminal drug concentration in each segment of the GI tract after oral administration was measured directly in fasted rats. Water ingested orally was absorbed quickly in the jejunum and the luminal fluid volume was diminished in the middle to lower part of the small intestine. According to the absorption of water luminal concentration of atenolol, a drug with low permeability, was elevated and exceeded the initial dose concentration. In contrast, the concentration of highly permeable drugs, antipyrine and metoprolol, decreased quickly in the upper part of the intestine and a significant amount of drugs was not detected in the lower jejunum and the ileum. From the time-profiles of luminal drug concentration, fraction of dose absorbed from each segment of the GI tract was calculated. Both antipyrine and metoprolol were found to be absorbed quickly at the upper part of the small intestine. In addition, the possible contribution of gastric absorption was demonstrated for these drugs. The pattern of site-dependent absorption of atenolol showed the higher absorbability in the middle and lower portion of the jejunum. These informations on site-dependent absorption of drugs are considered to be important for effective oral delivery systems.
机译:进行此项研究以评估口服后胃肠道(GI)中药物的吸收部位。通过原位单程灌注方法测量对大鼠肠,空肠,回肠和结肠不同区域的药物渗透性。揭示了上皮表面积不应决定高渗透性药物的肠渗透性的区域差异。研究了上皮表面粘液层和上皮细胞膜流动性对药物渗透性的影响。这些因素被证明有助于肠道药物渗透性的区域差异。口服后直接在禁食大鼠中测量胃肠道各段的腔内药物浓度。口服摄入的水在空肠中迅速吸收,小肠中部至下部的腔液量减少。根据水的吸收腔内阿替洛尔的浓度,具有低渗透性的药物被升高并超过了初始剂量浓度。相反,高渗透性药物安替比林和美托洛尔的浓度在肠道上部迅速下降,而在空肠下部和回肠未检测到大量药物。根据腔内药物浓度的时间曲线,计算从胃肠道各部分吸收的剂量比例。发现安替比林和美托洛尔均在小肠上部迅速吸收。此外,这些药物证明了胃吸收的可能作用。依赖部位的阿替洛尔吸收模式显示出在空肠中部和下部的较高吸收性。这些关于药物的部位依赖性吸收的信息被认为对于有效的口服递送系统很重要。

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