Department of Reproductive and Developmental Sciences, University of Trieste, and Institute of Child Health IRCCS Burlo Garofolo, Trieste, Italy.
Antimicrob Agents Chemother. 2010 Apr;54(4):1644-6. doi: 10.1128/AAC.01172-09. Epub 2010 Jan 19.
The pharmacokinetics of the aminoglycoside tobramycin was evaluated after oral administration to fed or fasting (15 h) mice. As expected, under normal feeding conditions, oral absorption was negligible; however, fasting induced a dramatic increase in tobramycin bioavailability. The dual-sugar test with lactulose and l-rhamnose confirmed increased small bowel permeability via the paracellular route in fasting animals. When experiments aimed at increasing the oral bioavailability of hydrophilic compounds are performed, timing of fasting should be extremely accurate.
我们评估了氨基糖苷类药物妥布霉素在给予进食或禁食(15 小时)小鼠后的药代动力学。正如预期的那样,在正常进食条件下,口服吸收可忽略不计;然而,禁食可显著增加妥布霉素的生物利用度。乳糖和 L-鼠李糖的双糖试验证实禁食动物通过细胞旁途径增加了小肠通透性。当进行旨在提高亲水性化合物口服生物利用度的实验时,禁食时间应非常准确。