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肾功能损害对醋酸艾司利卡西平药代动力学的影响。

Effect of renal impairment on the pharmacokinetics of eslicarbazepine acetate.

作者信息

Maia J, Almeida L, Falcão A, Soares E, Mota F, Potgieter M A, Potgieter J H, Soares-da-Silva P

机构信息

Department of Research and Development, BIAL (Portela & Ca SA), S. Mamede do Coronado, Portugal.

出版信息

Int J Clin Pharmacol Ther. 2008 Mar;46(3):119-30. doi: 10.5414/cpp46119.

Abstract

OBJECTIVE

Antiepileptic drugs are often used in patients with some degree of renal impairment. The objective of this study was to evaluate the effect of renal function on the pharmacokinetics of eslicarbazepine acetate (ESL, formerly known as BIA 2-093), a new antiepileptic drug under clinical development.

METHODS

ESL pharmacokinetics following 800 mg single dose was characterized in subjects with normal renal function (n=8, control group), and in patients with mild renal impairment (n=8), moderate renal impairment (n=8), severe renal impairment (n=8), and end-stage renal disease requiring hemodialysis (n=8).

RESULTS

ESL suffered extensive first-pass hydrolysis to eslicarbazepine (S-licarbazepine), the main active metabolite. While eslicarbazepine Cmax did not significantly differ between the different groups, the extent of systemic exposure, assessed by AUC, increased when renal function decreased. Eslicarbazepine CL/F and CLR were, respectively, 3.40 l/h and 1.04 l/h (17.3 ml/min) in the control group, and 2.10 l/h (35.0 ml/min) and 0.61 l/h (10.2 ml/min) in the mild, 1.60 l/h (26.7 ml/min) and 0.22 l/h (3.7 ml/min) in the moderate, and 1.33 l/h (21.2 ml/min) and 0.09 l/h (1.5 ml/min) in the severe renal impairment groups. Although the total amount of eslicarbazepine recovered in urine until 72 h post-dose was similar in the control and mild renal impairment groups, a decrease was found in the moderate and severe renal impairment groups. Major metabolites recovered in urine were eslicarbazepine and its glucuronide form. Clearance of minor metabolites (R-licarbazepine, oxcarbazepine and their glucuronides) was also dependent on renal function. In patients with end-stage renal disease, dialysis was effective in removing the ESL metabolites from the circulation.

CONCLUSIONS

ESL metabolites are excreted primarily by renal route and their clearance is dependent on renal function. ESL dosage adjustment may be necessary in patients with a creatinine clearance <60 ml/min.

摘要

目的

抗癫痫药物常用于有一定程度肾功能损害的患者。本研究的目的是评估肾功能对醋酸艾司利卡西平(ESL,原名BIA 2-093,一种正在进行临床开发的新型抗癫痫药物)药代动力学的影响。

方法

对肾功能正常的受试者(n = 8,对照组)、轻度肾功能损害患者(n = 8)、中度肾功能损害患者(n = 8)、重度肾功能损害患者(n = 8)以及需要血液透析的终末期肾病患者(n = 8)进行单剂量800 mg的ESL药代动力学特征研究。

结果

ESL在首过代谢过程中大量水解为主要活性代谢产物艾司利卡西平(S-利卡西平)。虽然不同组之间艾司利卡西平的Cmax无显著差异,但通过AUC评估的全身暴露程度在肾功能下降时增加。对照组中艾司利卡西平的CL/F和CLR分别为3.40 l/h和1.04 l/h(17.3 ml/min),轻度肾功能损害组分别为2.10 l/h(35.0 ml/min)和0.61 l/h(10.2 ml/min),中度肾功能损害组分别为1.60 l/h(26.7 ml/min)和0.22 l/h(3.7 ml/min),重度肾功能损害组分别为1.33 l/h(21.2 ml/min)和0.09 l/h(1.5 ml/min)。虽然给药后72小时内对照组和轻度肾功能损害组尿中回收的艾司利卡西平总量相似,但中度和重度肾功能损害组出现下降。尿中回收的主要代谢产物为艾司利卡西平及其葡萄糖醛酸结合物。次要代谢产物(R-利卡西平、奥卡西平及其葡萄糖醛酸结合物)的清除也依赖于肾功能。在终末期肾病患者中,透析可有效清除循环中的ESL代谢产物。

结论

ESL代谢产物主要通过肾脏途径排泄,其清除依赖于肾功能。肌酐清除率<60 ml/min的患者可能需要调整ESL剂量。

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