Nagai K, Fukuno S, Moriwaki R, Kuroda H, Omotani S, Miura T, Hatsuda Y, Myotoku M, Konishi H
Laboratory of Clinical Pharmacy and Therapeutics, Osaka Ohtani University, Tondabayashi, Japan;, Email:
Laboratory of Clinical Pharmacy and Therapeutics, Osaka Ohtani University, Tondabayashi, Japan.
Pharmazie. 2022 Apr 10;77(3):118-120. doi: 10.1691/2022.1756.
In the present study, we examined the effects of concurrent and staggered dosing of PG-soft ace-MP TM (PG), novel semi-solid enteral nutrients, on the pharmacokinetics of orally administered carbamazepine (CBZ) in rats due to the high possibility of drug interaction during the absorption process. The pharmacokinetic behavior of CBZ was considerably altered when administered concurrently with PG. The maximum serum CBZ concentration (C) significantly decreased and the mean residence time (MRT) significantly increased. The elimination constant (k) also significantly increased, but there were no significant changes in the area under the serum CBZ concentration time curve (AUC) and the time to reach C (T). However, these changes in the pharmacokinetic parameters were eliminated by waiting 20 min, the time interval equivalent to the T described above, between CBZ administration and PG dosing. This study suggested that PG interferes with CBZ absorption from the digestive tract, although staggered administration of CBZ and PG prevented their interaction.
在本研究中,由于吸收过程中存在药物相互作用的高可能性,我们研究了新型半固体肠内营养剂PG-soft ace-MP TM(PG)同时给药和错开给药对大鼠口服卡马西平(CBZ)药代动力学的影响。当与PG同时给药时,CBZ的药代动力学行为发生了显著改变。血清CBZ最大浓度(Cmax)显著降低,平均驻留时间(MRT)显著增加。消除常数(k)也显著增加,但血清CBZ浓度-时间曲线下面积(AUC)和达到Cmax的时间(Tmax)没有显著变化。然而,通过在CBZ给药和PG给药之间等待20分钟(与上述Tmax相当的时间间隔),消除了药代动力学参数的这些变化。本研究表明,PG会干扰CBZ从消化道的吸收,尽管错开CBZ和PG的给药可防止它们的相互作用。