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布比卡因在犬静脉注射和硬膜外给药后的处置及药理作用。

Bupivacaine disposition and pharmacologic effects after intravenous and epidural administrations in dogs.

作者信息

Franquelo C, Toledo A, Manubens J, Cristòfol C, Arboix M

机构信息

Divisió de Farmacologia, Facultat de Veterinària, UAB, Rubi (Toledo), Spain.

出版信息

Am J Vet Res. 1995 Aug;56(8):1087-91.

PMID:8533982
Abstract

Pharmacokinetic variables of bupivacaine (BPV) were determined after IV and epidural administrations in the same 6 dogs. Plasma BPV concentration curves after IV administration were adjusted to biexponential kinetics: a rapid distribution phase was followed by a slower elimination phase, with half-life of 34.5 +/- 7.8 minutes. Mean plasma clearance was 20.2 +/- 7.4 ml/min/kg of body weight, and mean volume of distribution at steady state was 0.7 +/- 0.2 L/kg. After epidural administration, absorption was rapid. Peak plasma concentration, 1.4 +/- 0.4 microgram/ml, was detected approximately 5 minutes after BPV administration. The half-life corresponding to epidural administration (179 +/- 33.6 minutes) was 5 to 6 times longer than that observed after IV administration, possibly because of the slow release of BPV from the epidural space. Induction times were short (2.3 +/- 2.2 minutes); anesthesia quickly began and lasted for more than 2 hours (158 +/- 48.8 minutes). During that period, BPV plasma concentration ranged between 1.4 and 0.2 microgram/ml. Changes in systolic blood pressure and heart rate were correlated to high plasma concentration of BPV. These modifications were observed for the first 30 minutes, reaching baseline values after 60 minutes.

摘要

在同6只犬中静脉注射和硬膜外注射布比卡因(BPV)后测定其药代动力学变量。静脉注射后血浆BPV浓度曲线调整为双指数动力学:快速分布相后是较慢的消除相,半衰期为34.5±7.8分钟。平均血浆清除率为20.2±7.4毫升/分钟/千克体重,稳态分布容积平均为0.7±0.2升/千克。硬膜外注射后,吸收迅速。在BPV给药后约5分钟检测到血浆峰浓度为1.4±0.4微克/毫升。硬膜外注射对应的半衰期(179±33.6分钟)比静脉注射后观察到的半衰期长5至6倍,可能是因为BPV从硬膜外腔缓慢释放。诱导时间短(2.3±2.2分钟);麻醉迅速开始并持续超过2小时(158±48.8分钟)。在此期间,BPV血浆浓度在1.4至0.2微克/毫升之间。收缩压和心率的变化与BPV的高血浆浓度相关。这些改变在最初30分钟观察到,60分钟后达到基线值。

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