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Alterations in Pharmacokinetics of Orally Administered Carbamazepine in Rats Treated with Sodium alginate: Possible Interaction between Therapeutic Drugs and Semi-solid Enteral Nutrients

机译:用藻酸钠治疗的大鼠口服尿道药代动力学的改变:治疗药物和半固体肠内营养素之间的可能相互作用

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Objective 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. Method 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. Findings 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_(e)) among the groups. In the in vitro assay, CBZ was adsorbed by SA in the solution used to reflect fluid in the intestinal tract. Conclusions 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.
机译:目的利用肠内营养素在准确的营养管理中起着极其重要的作用。藻酸钠(SA)经常用于肠内营养素的半凝固。在本研究中,我们研究了口服施用的猪氨基(CBZ)的药代动力学谱是否通过在药物的给药之前和之后的SA治疗来改变。此外,使用体外分析检查SA对CBZ的吸附效应。在CBZ给药后立即向大鼠口服施用方法SA。通过非室内方法分析其口服给药后的CBZ浓度谱。使用超滤装置在离心后评价CBZ在SA上的吸附。通过用SA处理减少每个取样点处的口服施用CBZ的血清浓度,并且当在给予药物后立即摄入SA时,在CBZ浓度下观察到的降低程度较大,这与在曲线(AUC)下区域的值中观察到的改变。在组中的末端阶段(K_(e))的消除速率下没有注意到的显着差异。在体外测定中,CBZ通过SA吸附在用于反射肠道中的流体的溶液中。结论SA通过药代动力学相互作用,CBZ的药理学效果可能降低,并且应仔细关注施用CBZ和半固体肠内营养素的时间。

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