Hollander D, Dadufalza V D, Fairchild P A
J Lab Clin Med. 1981 Oct;98(4):591-8.
The small intestinal absorption of aspirin at pharmacological concentrations was studied in the unanesthetized rat by using a single-pass perfusion technique. The rate of aspirin absorption remained linear with its concentration (0.5 to 10 mM). Intestinal aspirin absorption increased as the concentration of hydrogen ion, sodium taurocholate, and ascorbic acid in the perfusate increased. Aspirin absorption did not change after ethanol addition. At pH 3.5 or 6.5, intestinal absorption of aspirin was greater than gastric absorption of the compound. Aspirin was not absorbed by the stomach at pH 6.5. These experiments indicate that aspirin can be absorbed to an appreciable extent in its ionized form by the small intestine but not by the stomach.
采用单通道灌注技术,在未麻醉的大鼠身上研究了药理浓度下阿司匹林的小肠吸收情况。阿司匹林的吸收速率与其浓度(0.5至10 mM)呈线性关系。随着灌注液中氢离子、牛磺胆酸钠和抗坏血酸浓度的增加,肠道对阿司匹林的吸收增加。添加乙醇后,阿司匹林的吸收没有变化。在pH 3.5或6.5时,肠道对阿司匹林的吸收大于胃对该化合物的吸收。在pH 6.5时,胃不吸收阿司匹林。这些实验表明,阿司匹林可以以离子化形式在小肠中被大量吸收,但在胃中则不会。