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肾脏疾病、年龄与奥沙西泮的药代动力学

Renal disease, age, and oxazepam kinetics.

作者信息

Murray T G, Chiang S T, Koepke H H, Walker B R

出版信息

Clin Pharmacol Ther. 1981 Dec;30(6):805-9. doi: 10.1038/clpt.1981.241.

Abstract

Effects of renal insufficiency and age on oxazepam kinetics were assessed in 13 normal subjects (21 to 72 yr old), four patients with renal insufficiency, and eight patients on hemodialysis. Normal intact oxazepam results were: mean elimination half-life (t1/2), 10 hr; area under the curve (AUC), 6.0 microgram.hr/ml; unbound oxazepam fraction (fup), 3.2%; maximum concentration of unbound oxazepam (Cmax,u), 16 ng/ml; and intrinsic (unbound drug) clearance (Clint), 2.9 l/hr/kg. Less than 1% of the dose was excreted intact in urine. Age differences had no influence on results. In renal insufficiency patients, t1/2 was prolonged to 25 hr, fup increased to 7%, and Cmax,u and Clint were unchanged. Volume of distribution of unbound oxazepam (Vu) increased, thereby prolonging t1/2. In dialysis patients, t1/2 was prolonged to 33 hr, fup increased to 6.2%, and Cmax,u and Clint again were unchanged. Oxazepam was undialyzable; since unbound oxazepam disposition kinetics are not altered, no dosage adjustment for patients is necessary.

摘要

在13名正常受试者(21至72岁)、4名肾功能不全患者和8名接受血液透析的患者中评估了肾功能不全和年龄对奥沙西泮动力学的影响。正常完整奥沙西泮的结果为:平均消除半衰期(t1/2)为10小时;曲线下面积(AUC)为6.0微克·小时/毫升;未结合奥沙西泮分数(fup)为3.2%;未结合奥沙西泮的最大浓度(Cmax,u)为16纳克/毫升;固有(未结合药物)清除率(Clint)为2.9升/小时/千克。不到1%的剂量以原形从尿液中排泄。年龄差异对结果无影响。在肾功能不全患者中,t1/2延长至25小时,fup增加至7%,Cmax,u和Clint不变。未结合奥沙西泮的分布容积(Vu)增加,从而延长了t1/2。在透析患者中,t1/2延长至33小时,fup增加至6.2%,Cmax,u和Clint再次不变。奥沙西泮不可透析;由于未结合奥沙西泮的处置动力学未改变,因此无需对患者进行剂量调整。

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