Seegers J M, Olling M, Jager L P, Van Noordwijk J
J Pharm Sci. 1980 Aug;69(8):900-6. doi: 10.1002/jps.2600690811.
To study the pharmacokinetic interactions between aspirin (250 mg/kg) and simultaneously administered oral acetaminophen (125 mg/kg) or caffeine (50 mg/kg) in male rats, noninterfering GLC assays for these drugs were developed. Acetaminophen and caffeine both retarded the appearance of salicylate in plasma. During the elimination phase, acetaminophen enhanced plasms salicylate levels whereas caffeine did not. Aspirin reduced the plasms levels of both acetaminophen and caffeine during absorption and elimination. Regardless of whether the drugs had been administered separately or in combination, higher concentrations of salicylate, acetaminophen, and caffeine were found in the glandular part of the stomach compared to the nonglandular part (rumen). In both parts, the absorption of acetaminophen increased in the presence of aspirin. Simultaneous administration of aspirin with caffeine did not influence the absorption of either drug in the glandular and ruminal parts. The inhibitory action of acetaminophen and the potentiating action of caffeine on the erosive activity of aspirin are not due to any effects of these drugs on salicylate accumulation in glandular tissue.
为研究阿司匹林(250毫克/千克)与同时给予的口服对乙酰氨基酚(125毫克/千克)或咖啡因(50毫克/千克)在雄性大鼠体内的药代动力学相互作用,开发了针对这些药物的无干扰气相色谱分析法。对乙酰氨基酚和咖啡因均延迟了血浆中水杨酸盐的出现。在消除阶段,对乙酰氨基酚提高了血浆水杨酸盐水平,而咖啡因则没有。阿司匹林在吸收和消除过程中降低了对乙酰氨基酚和咖啡因的血浆水平。无论药物是单独给药还是联合给药,与非腺胃部(瘤胃)相比,腺胃部的水杨酸盐、对乙酰氨基酚和咖啡因浓度更高。在两个部位,阿司匹林存在时对乙酰氨基酚的吸收均增加。阿司匹林与咖啡因同时给药不影响腺胃部和瘤胃中任何一种药物的吸收。对乙酰氨基酚的抑制作用和咖啡因对阿司匹林侵蚀活性的增强作用并非由于这些药物对腺组织中水杨酸盐积累的任何影响。