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头孢羟氨苄的肾脏排泄机制研究。

Studies on the renal excretion mechanisms of cefadroxil.

作者信息

Granero L, Gimeno M J, Torres-Molina F, Chesa-Jiménez J, Peris J E

机构信息

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of Valencia, Spain.

出版信息

Drug Metab Dispos. 1994 May-Jun;22(3):447-50.

PMID:8070323
Abstract

The mechanisms of renal excretion of cefadroxil were investigated in conscious rats. The drug was intravenously infused at several infusion rates (0.27, 1.08, 5.40, 12.00, and 31.35 mg/hr), and the total and renal clearances were determined after the steady-state was reached. Renal clearance accounted for approximately 91% of total clearance. Renal clearance of cefadroxil increased from 2.51 +/- 0.39 to 3.57 +/- 0.43 ml/min as the steady-state cefadroxil plasma concentration increased from 1.7 +/- 0.3 to 24.4 +/- 3.8 micrograms/ml, and this has been attributed to a saturable renal tubular reabsorption of the antibiotic. The ratio of unbound cefadroxil renal clearance to glomerular filtration rate was larger than unity, which indicates that the antibiotic also undergoes active renal tubular secretion. When cefadroxil was administered together with cephalexin, an increase in the renal clearance of cefadroxil was observed, which has been attributed to a competitive inhibition of the tubular reabsorption of cefadroxil by cephalexin. A pharmacokinetic model for the renal excretion of cefadroxil was developed, and mathematical expressions showing the relationship between renal clearance and steady-state plasma concentration were deduced.

摘要

在清醒大鼠中研究了头孢羟氨苄的肾排泄机制。以几种输注速率(0.27、1.08、5.40、12.00和31.35毫克/小时)静脉输注该药物,在达到稳态后测定总清除率和肾清除率。肾清除率约占总清除率的91%。随着头孢羟氨苄稳态血浆浓度从1.7±0.3微克/毫升增加到24.4±3.8微克/毫升,头孢羟氨苄的肾清除率从2.51±0.39毫升/分钟增加到3.57±0.43毫升/分钟,这归因于抗生素的肾小管重吸收存在饱和现象。未结合的头孢羟氨苄肾清除率与肾小球滤过率之比大于1,这表明该抗生素也经历肾小管主动分泌。当头孢羟氨苄与头孢氨苄一起给药时,观察到头孢羟氨苄的肾清除率增加,这归因于头孢氨苄对头孢羟氨苄肾小管重吸收的竞争性抑制。建立了头孢羟氨苄肾排泄的药代动力学模型,并推导了显示肾清除率与稳态血浆浓度之间关系的数学表达式。

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