Carlson Amy M, Kelly Richard, Fetterer David P, Rico Pedro J, Bailey Emily J
Veterinary Medicine Division, The United States Army Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Statistics, The United States Army Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
J Am Assoc Lab Anim Sci. 2016;55(4):436-42.
Fentanyl is a μ-opioid agonist that often is used as the analgesic component for balanced anesthesia in both human and veterinary patients. Minimal information has been published regarding appropriate dosing, and the pharmacokinetics of fentanyl are unknown in NHP. The pharmacokinetic properties of 2 transdermal fentanyl delivery methods, a solution (2.6 and 1.95 mg/kg) and a patch (25 μg/h), were determined when applied topically to the dorsal scapular area of cynomolgus macaques (Macaca fascicularis). Serum fentanyl concentrations were analyzed by using liquid chromatography-mass spectrometry. Compared with the patch, the transdermal fentanyl solution generated higher drug concentrations over longer time. Adverse reactions occurred in the macaques that received the transdermal fentanyl solution at 2.6 mg/kg. Both preparations showed significant interanimal variability in the maximal serum drug levels, time to achieve maximal fentanyl levels, elimination half-life, and AUC values. Both the maximal concentration and the time at which this concentration occurred were increased in macaques compared with most other species after application of the transdermal fentanyl patch and compared with dogs after application of the transdermal fentanyl solution. The pharmacokinetic properties of transdermal fentanyl in macaques are markedly different from those in other veterinary species and preclude its use as a long-acting analgesic drug in NHP.
芬太尼是一种μ阿片受体激动剂,常用于人类和兽医患者的平衡麻醉镇痛成分。关于合适剂量的公开信息极少,且食蟹猴的芬太尼药代动力学尚不清楚。将两种透皮芬太尼给药方法,即溶液(2.6和1.95mg/kg)和贴剂(25μg/h)局部应用于食蟹猴(猕猴)肩胛背部区域后,测定其药代动力学特性。采用液相色谱 - 质谱法分析血清芬太尼浓度。与贴剂相比,透皮芬太尼溶液在更长时间内产生更高的药物浓度。接受2.6mg/kg透皮芬太尼溶液的猕猴出现了不良反应。两种制剂在最大血清药物水平、达到最大芬太尼水平的时间、消除半衰期和AUC值方面均表现出显著的动物间变异性。与应用透皮芬太尼贴剂后的大多数其他物种相比,以及与应用透皮芬太尼溶液后的犬类相比,猕猴应用后最大浓度及其出现时间均有所增加。透皮芬太尼在猕猴体内的药代动力学特性与其他兽医物种明显不同,因此不能将其用作食蟹猴的长效镇痛药。