Veng-Pedersen P, Wilhelm J A, Zakszewski T B, Osifchin E, Waters S J
College of Pharmacy, University of Iowa, Iowa City 52242, USA.
J Pharm Sci. 1995 Sep;84(9):1101-6. doi: 10.1002/jps.2600840913.
A continuous fentanyl infusion was administered to eight adult, male beagle dogs for a duration of approximately 400 min at a rate of 30 micrograms/kg/h. The extent of respiratory depression was quantified by continuous, noninvasive, transcutaneous pCO2 recordings. Upon reaching a pseudosteady-state of respiratory depression at approximately 120 min of fentanyl infusion, the animals then received, in a 2 x 2 crossover fashion separated by approximately 3 weeks, 30-minute equiefficacious infusions of nalmefene (12 micrograms/kg/h) or naloxone (48 micrograms/kg/h). Multiple venous blood samples were taken throughout the dosing regimen, and the resulting fentanyl, nalmefene, or naloxone plasma concentrations were determined. The concentration-time data were analyzed by noncompartmental methods and subsequently linked to the pharmacodynamic effect data by a competitive antagonism link model. Separately, the biophase concentrations were linked to the plasma concentration-time profiles through a single-exponential conduction function. The various pharmacokinetic/pharmacodynamic parameters resulting from this semiparametric analysis were analyzed by ANOVA, using a statistical model that considers carryover effects. The results of these analyses indicate that several pharmacokinetic/pharmacodynamic parameters of the two antagonists were comparable. However, nalmefene had a significantly more protracted terminal disposition and a significantly greater persistency in the biophase evaluated over the experimental time frame from 0 to 450 min.
以30微克/千克/小时的速率对8只成年雄性比格犬持续输注芬太尼约400分钟。通过连续、无创的经皮二氧化碳记录对呼吸抑制程度进行量化。在芬太尼输注约120分钟达到呼吸抑制的假稳态后,动物以2×2交叉方式接受纳美芬(12微克/千克/小时)或纳洛酮(48微克/千克/小时)的30分钟等效剂量输注,两次输注间隔约3周。在整个给药方案过程中采集多个静脉血样,测定所得的芬太尼、纳美芬或纳洛酮血浆浓度。浓度-时间数据采用非房室方法进行分析,随后通过竞争性拮抗连接模型与药效学效应数据相关联。另外,通过单指数传导函数将生物相浓度与血浆浓度-时间曲线相关联。采用考虑残留效应的统计模型,通过方差分析对该半参数分析得到的各种药代动力学/药效学参数进行分析。这些分析结果表明,两种拮抗剂的几个药代动力学/药效学参数具有可比性。然而,在0至450分钟的实验时间范围内评估,纳美芬在生物相中的终末处置明显更持久,持续性明显更强。