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一种研究啮齿动物肝脏药物代谢的非侵入性方法:大鼠氨基比林代谢

A noninvasive method for the study of hepatic drug metabolism in rodents: aminopyrine metabolism in rats.

作者信息

Moldowan M J

出版信息

Pharmacology. 1983;26(6):331-6. doi: 10.1159/000137819.

Abstract

A rapid, sensitive, and simple high-performance liquid chromatography method is described for the direct analysis of aminopyrine in saliva. The detection limit was found to be 12 ng/ml of sample. Accuracy and precision were maintained with as little as 1 microliter of saliva. Thus the rate of elimination of aminopyrine has been monitored noninvasively in rats. The aminopyrine half-life was found to be 59.5 +/- 10.5 (SD) min. The half-life was independent of an aminopyrine dose between 50 and 200 mg/kg. In rats single intraperitoneal doses of SKF 525-A (20 mg/kg) produced increases in aminopyrine half-life and salivary aminopyrine concentration. Phenobarbital induction lowered the aminopyrine half-life to 33.2 +/- 8.5 min and the salivary aminopyrine concentration.

摘要

本文描述了一种快速、灵敏且简便的高效液相色谱法,用于直接分析唾液中的氨基比林。检测限为每毫升样品12纳克。仅需1微升唾液就能保持准确度和精密度。因此,已对大鼠体内氨基比林的消除速率进行了非侵入性监测。发现氨基比林的半衰期为59.5±10.5(标准差)分钟。半衰期与50至200毫克/千克之间的氨基比林剂量无关。在大鼠中,单次腹腔注射SKF 525-A(20毫克/千克)会使氨基比林半衰期和唾液中氨基比林浓度增加。苯巴比妥诱导可将氨基比林半衰期降至33.2±8.5分钟,并降低唾液中氨基比林浓度。

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