Pharmacokinetic profile of etodolac in special populations.

L Z Benet
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Abstract

The pharmacokinetics of etodolac in healthy normal volunteers has been extensively studied and is well described. Etodolac is characterised by a high oral bioavailability, low clearance, a small volume of distribution, and a 7-hour half-life. It is essentially completely metabolised, therefore little is excreted unchanged. Etodolac is highly protein bound. To investigate the effect of disease states or concomitant drug administration on a patient's response to etodolac, additional pharmacokinetic studies were carried out in special populations. Since etodolac has a well-defined pharmacokinetic-pharmacodynamic relationship, measurement of pharmacokinetic parameters is clinically relevant. Data from studies to date show that disease states, underlying conditions, and concomitantly administered highly protein-bound drugs have essentially no effect on etodolac pharmacokinetics. Therefore, etodolac can generally be given without the need for dosage modifications in special populations such as uncompromised elderly patients, those with moderate renal impairment, and patients with stable hepatic disease.

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依托多拉酸在特殊人群中的药代动力学特征。
依托多拉酸在健康正常志愿者体内的药代动力学已经得到了广泛的研究和很好的描述。依托度酸的特点是口服生物利用度高,清除率低,分布体积小,半衰期为7小时。它基本上是完全代谢,因此很少是不变的排泄。依托度酸是高度蛋白结合的。为了研究疾病状态或伴随药物给药对患者对依托度酸反应的影响,在特殊人群中进行了额外的药代动力学研究。由于依托度酸具有明确的药代动力学-药效学关系,因此测量药代动力学参数具有临床意义。迄今为止的研究数据表明,疾病状态、潜在条件和伴随使用的高蛋白结合药物基本上对依托多拉酸的药代动力学没有影响。因此,对于特殊人群,如未受损的老年患者、中度肾功能损害患者和稳定型肝病患者,通常无需调整剂量即可给予依托度酸。
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