Serum Pharmacokinetics of a Highly Concentrated Buprenorphine Formulation in Older Female Sprague-Dawley Rats (Rattus norvegicus).

Kristopher G Galang, Heather K Knych, Rhonda S Oates
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Abstract

Laboratory rats (Rattus norvegicus) are common animal models used in biomedical, psychological, and toxicological research. Their long-established research use has driven the progressive refinement of experimental techniques so that associated pain/distress may be ameliorated. One of these refinements is the use of opioids to provide analgesia. Buprenorphine, a partial mu-opioid agonist with high affinity for mu receptors, is commonly used for rodents, as the longer duration of action compared with morphine reduces the need for direct handling during administration of supplemental doses. While conventional buprenorphine (CB) requires dosing two to four times per day to provide sufficient pain control in many mammalian species, a novel, highly concentrated formulation of buprenorphine (HCB; Simbadol) is the first FDA-approved, veterinary-specific opioid labeled for every 24-hour dosing in cats (Felis catus). We hypothesized that, at the labeled feline dose of 0.24 mg/kg SC, HCB would achieve buprenorphine serum concentrations ≥1 ng/mL in older adult female Sprague-Dawley rats for at least 12 to 24 hours. Mean peak serum concentrations of 13.79 ± 6.76 ng/mL occurred 0.5 hour after administration. Twelve hours postadministration, the mean serum concentration was 2.12 ± 0.59 ng/mL with all treated rats maintaining individual serum concentrations well above 1 ng/mL. Twenty-four hours postadministration, the mean serum concentration was 1.02 ± 0.33 ng/mL with 4 of 6 rats maintaining individual serum concentrations of greater than or equal to 0.99 ng/mL. With the exception of a minor, focal injection site reaction in one animal, none of the other known side effects of opioid administration in rats were observed. These results support that administration of HCB at 0.24 mg/kg SC to older adult female SD rats produces serum buprenorphine concentrations consistent with analgesia for at least 12 hours and for up to 24 hours in some rats.

高浓度丁丙诺啡制剂在老年雌性Sprague-Dawley大鼠(褐家鼠)体内的血清药代动力学。
褐家鼠(Rattus norvegicus)是生物医学、心理学和毒理学研究中常用的动物模型。它们长期建立的研究用途推动了实验技术的逐步完善,从而可以改善相关的疼痛/痛苦。其中一个改进是使用阿片类药物来提供镇痛。丁丙诺啡是一种对mu受体具有高亲和力的部分mu-阿片激动剂,通常用于啮齿类动物,因为与吗啡相比,作用时间更长,在给药期间减少了直接处理的需要。传统的丁丙诺啡(CB)需要每天服用两到四次才能在许多哺乳动物中提供足够的疼痛控制,而一种新型的、高度浓缩的丁丙诺啡(HCB; Simbadol)是第一个经fda批准的、兽医专用的阿片类药物,每24小时给猫服用一次。我们假设,在标记猫剂量为0.24 mg/kg SC的情况下,HCB可以使老年雌性Sprague-Dawley大鼠的丁丙诺啡血清浓度≥1 ng/mL至少12至24小时。给药后0.5小时平均血药浓度峰值为13.79±6.76 ng/mL。给药12小时后,平均血清浓度为2.12±0.59 ng/mL,所有给药大鼠的个体血清浓度均保持在1 ng/mL以上。给药24小时后,平均血清浓度为1.02±0.33 ng/mL, 6只大鼠中有4只维持大于或等于0.99 ng/mL的个体血清浓度。除了在一只动物中出现轻微的局灶性注射部位反应外,在大鼠中没有观察到阿片类药物给药的其他已知副作用。这些结果支持,给成年雌性SD大鼠0.24 mg/kg剂量的HCB使血清丁丙诺啡浓度与镇痛至少12小时一致,在一些大鼠中可达24小时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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