Nagai Katsuhito, Omotani Sachiko, Ito Akihiko, Nishimura Ikumi, Hatsuda Yasutoshi, Mukai Junji, Teramachi Hitomi, Myotoku Michiaki
Faculty of Pharmacy, Laboratory of Practical Pharmacy and Pharmaceutical Care, Osaka Ohtani University, Tondabayashi, Japan.
Department of gastroenterology, National Hospital Organization Higashi-Ohmi General Medical Center, Higashiomi, Japan.
Drug Res (Stuttg). 2019 Feb;69(3):168-172. doi: 10.1055/a-0662-5701. Epub 2018 Aug 13.
The use of enteral nutrients plays an extremely important role in accurate nutrition management. Sodium alginate (SA) is frequently used for the semi-solidification of enteral nutrients. In the present study, we investigated whether the pharmacokinetic profile of orally administered carbamazepine (CBZ) is altered by a treatment with SA immediately before and after dosing of the drug. Furthermore, the adsorption effects of SA on CBZ were examined using an in vitro analysis.
SA was orally administered to rats just before and immediately after CBZ dosing. The CBZ concentration profile following its oral administration was analyzed by a non-compartmental method. The adsorption of CBZ onto SA was evaluated after centrifugation using an ultrafiltration device.
The serum concentration of orally administered CBZ at each sampling point was reduced by the treatment with SA, and the extent of the decrease observed in the concentration of CBZ was larger when SA was ingested immediately after administration of the drug, which was consistent with the alteration observed in the value of the area under the curve (AUC). No significant differences were noted in the elimination rate at the terminal phase (k) among the groups. In the in vitro assay, CBZ was adsorbed by SA in the solution used to reflect fluid in the intestinal tract.
The pharmacological efficacies of CBZ might be reduced by SA through the pharmacokinetic interactions, and that the careful attention should be paid to the timing of administration of CBZ and semi-solid enteral nutrients.
肠内营养物质的使用在精准营养管理中发挥着极其重要的作用。海藻酸钠(SA)常用于肠内营养物质的半固化。在本研究中,我们调查了在给药前后立即用SA治疗是否会改变口服卡马西平(CBZ)的药代动力学特征。此外,使用体外分析研究了SA对CBZ的吸附作用。
在给CBZ之前和之后立即给大鼠口服SA。采用非房室模型方法分析口服CBZ后的浓度变化情况。使用超滤装置离心后评估CBZ在SA上的吸附情况。
在每个采样点,口服CBZ的血清浓度因SA治疗而降低,并且在给药后立即摄入SA时,观察到的CBZ浓度下降幅度更大,这与曲线下面积(AUC)值的变化一致。各组间终末相消除率(k)无显著差异。在体外试验中,在用于反映肠道内液体的溶液中,CBZ被SA吸附。
SA可能通过药代动力学相互作用降低CBZ的药理疗效,因此应谨慎注意CBZ与半固体肠内营养物质的给药时间。