Chae J-W, Song B-J, Baek I-H, Yun H-Y, Ma J Y, Kwon K-I
College of Pharmacy, Chungnam National University, Daejeon, Korea.
College of Pharmacy, Kyungsung University, Busan, Korea.
J Vet Pharmacol Ther. 2015 Oct;38(5):497-9. doi: 10.1111/jvp.12200. Epub 2015 Jan 27.
This study was performed to determine the pharmacokinetic profile of mosapride in fasting and fed states. A single 5-mg oral dose of mosapride was administered to fasted (n = 15) and fed (n = 12) beagle dogs, and the plasma concentrations of mosapride were measured by liquid chromatography-tandem mass spectrometry. The resultant data were analyzed by noncompartmental analysis (NCA). Mosapride was absorbed in fasted and fed dogs with similar Tmax . Both Cmax and AUC were significantly higher in the fasting group than in fed dogs, being four times (10.51 μg/mL vs. 2.76 μg/mL) and 3.5 times higher (38.53 h · μg/mL vs. 10.22 h · μg/mL), respectively. These findings suggest that food intake affects the pharmacokinetics of mosapride and that the dosage regimen for this drug need to be reconsidered.
本研究旨在确定莫沙必利在禁食和进食状态下的药代动力学特征。对15只禁食和12只进食的比格犬口服单次5毫克莫沙必利,并采用液相色谱 - 串联质谱法测定血浆中莫沙必利的浓度。所得数据通过非房室分析(NCA)进行分析。莫沙必利在禁食和进食的犬中均被吸收,Tmax相似。禁食组的Cmax和AUC均显著高于进食犬,分别高出四倍(10.51μg/mL对2.76μg/mL)和3.5倍(38.53 h·μg/mL对10.22 h·μg/mL)。这些发现表明食物摄入会影响莫沙必利的药代动力学,需要重新考虑该药物的给药方案。