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Pharmacokinetics of buccal mucosal administration of fentanyl in a carboxymethylcellulose gel compared with IV administration in dogs

机译:与犬静脉注射相比,羧甲基纤维素凝胶中的芬太尼经颊粘膜给药的药代动力学

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摘要

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.
机译:评价了芬太尼静脉注射(0.01 mg / kg)和羧甲基纤维素凝胶(0.05 mg / kg)应用于六只健康的成年中型至大型犬的颊粘膜的药代动力学。经粘膜(TM)给药后5分钟,所有狗的血清芬太尼水平均达到治疗目标以上(0.95 ng / ml)。除了与芬太尼相关的治疗靶点上方更长的血清芬太尼浓度持续时间外,静脉输注芬太尼和TM芬太尼之间均未发现明显的药代动力学差异。 TM芬太尼可以快速达到血清芬太尼浓度,被认为是IV给药的无创替代药物。

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