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戊巴比妥在犬体内的药代动力学。

Pharmacokinetics of pentobarbital in the dog.

作者信息

Frederiksen M C, Henthorn T K, Ruo T I, Atkinson A J

出版信息

J Pharmacol Exp Ther. 1983 May;225(2):355-60.

PMID:6842399
Abstract

The pharmacokinetics of pentobarbital were studied after i.v. administration of a 30-mg/kg dose to five dogs. Pentobarbital plasma concentrations were measured with a new gas chromatographic method, utilizing on-column methylation of pentobarbital and as a butabarbital internal standard. The kinetics of pentobarbital distribution and elimination were analyzed with a three-compartment open mammillary model. The elimination-phase half-life of pentobarbital was 8.2 +/- 2.2 hr. The steady-state volume of pentobarbital distribution was 1.08 +/- 0.21 liters/kg and the elimination clearance was 0.0013 +/- 0.0004 liters/min X kg. Threshold pentobarbital concentrations required to suppress the corneal reflex and withdrawal response to pain were 26.4 +/- 4.6 and 23.0 +/- 2.9 micrograms/ml, respectively. These results should facilitate the design of i.v. anesthetic regimens with pentobarbital.

摘要

给五只狗静脉注射30毫克/千克剂量的戊巴比妥后,对其药代动力学进行了研究。采用一种新的气相色谱法测定戊巴比妥血浆浓度,该方法利用戊巴比妥的柱上甲基化并以丁巴比妥作为内标。用三室开放乳头模型分析戊巴比妥的分布和消除动力学。戊巴比妥的消除相半衰期为8.2±2.2小时。戊巴比妥分布的稳态容积为1.08±0.21升/千克,消除清除率为0.0013±0.0004升/分钟×千克。抑制角膜反射和对疼痛的退缩反应所需的戊巴比妥阈值浓度分别为26.4±4.6和23.0±2.9微克/毫升。这些结果应有助于设计戊巴比妥静脉麻醉方案。

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