羧甲基纤维素凝胶芬太尼口腔黏膜给药与静脉给药的药代动力学比较。

Veterinary Therapeutics Pub Date : 2008-01-01
Amy A Little, Ursula Krotscheck, Dawn M Boothe, Hollis N Erb
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引用次数: 0

摘要

研究了芬太尼静脉给药(0.01 mg/kg)和羧甲基纤维素凝胶给药(0.05 mg/kg)在6只健康成年中大型犬口腔黏膜的药代动力学。经黏膜(TM)给药后5分钟,所有狗的血清芬太尼水平均高于治疗目标(0.95 ng/ml)。除了与TM给药相关的血清芬太尼浓度高于治疗靶点的持续时间较长外,IV和TM芬太尼之间没有明显的药代动力学差异。TM芬太尼可以被认为是一种非侵入性的静脉给药,可以快速达到血清芬太尼浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics of buccal mucosal administration of fentanyl in a carboxymethylcellulose gel compared with IV administration in dogs.

The pharmacokinetics of fentanyl administrated IV (0.01 mg/kg) and in a carboxymethylcellulose gel (0.05 mg/kg) applied to the buccal mucosa of six healthy adult medium- to large-breed dogs was evaluated. At 5 minutes after transmucosal (TM) administration, serum fentanyl levels above the therapeutic target (0.95 ng/ml) were achieved in all dogs. Except for the longer duration of serum fentanyl concentrations above the therapeutic target associated with TM administration, no significant pharmacokinetic differences were found between IV and TM fentanyl. TM fentanyl may be considered a noninvasive alternative to IV administration with rapid achievement of serum fentanyl concentrations.

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