同时和交错给药半固体营养物对大鼠口服卡马西平药代动力学的影响。

K. Nagai, S. Fukuno, R. Moriwaki, H. Kuroda, S. Omotani, T. Miura, Y. Hatsuda, M. Myotoku, H. Konishi
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引用次数: 0

摘要

在本研究中,我们研究了同时和交错给药PG-soft ace-MP TM (PG),一种新型半固体肠内营养物质,对大鼠口服卡马西平(CBZ)的药代动力学的影响,因为在吸收过程中药物相互作用的可能性很高。与PG同时给药时,CBZ的药动学行为明显改变,血清CBZ最大浓度(Cmax)显著降低,平均停留时间(MRT)显著增加。消除常数(ke)也显著升高,但血清CBZ浓度-时间曲线下面积(AUC)和到达Cmax的时间(Tmax)无显著变化。然而,在CBZ给药和PG给药之间等待20分钟(相当于上述Tmax的时间间隔),这些药代动力学参数的变化被消除了。本研究表明PG干扰CBZ从消化道的吸收,尽管CBZ和PG的交错给药阻止了它们的相互作用。
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Influence of concurrent and staggered dosing of semi-solid nutrients on the pharmacokinetics of orally administered carbamazepine in rats.
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 (Cmax) significantly decreased and the mean residence time (MRT) significantly increased. The elimination constant (ke) also significantly increased, but there were no significant changes in the area under the serum CBZ concentration versus time curve (AUC) and the time to reach Cmax (Tmax). However, these changes in the pharmacokinetic parameters were eliminated by waiting 20 min, the time interval equivalent to the Tmax 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.
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