Evaluation of Extended- and Immediate-Release Buprenorphine Formulations on Pharmacokinetics and Injection Site Lesions in Different Strains and Sex of Mice.

Susan Bolin, Wayne R Buck, Yan Sun, Donna Strasburg, Paige Ebert, DeAnne Stolarik, Yue-Ting Wang, Natalie Bratcher-Petersen, Sarah Clark
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Abstract

Buprenorphine is a commonly used analgesic in laboratory rodents for procedures of moderate to severe pain. We evaluated the pharmacokinetic properties of an immediate-release formulation of buprenorphine (Bup-IR) and an extended-release formulation (Bup-ER) in both sexes of 4 different strains of mice (C57BL/6, CD-1, BALB/c, and CB17 SCID) commonly used for dermatology and oncology research at our institution. Skin at the injection site was evaluated for 7 days postinoculation and scored for reactions and then collected for histopathologic analyses. Body weights were evaluated at 1 and 4 days postinoculation. We hypothesized that the administration of Bup-ER would provide a longer duration of blood drug concentration (>1 ng/mL; minimum analgesia threshold) compared with single-dose Bup-IR. We analyzed the standard dose for Bup-IR (0.3 mg/kg) and for Bup-ER (1 mg/kg), along with saline vehicle with blood collected at 1, 4, 24, 48, 72, and 96 hours following administration of Bup-ER and 0.25, 0.5, 1, 2, 3, 6, 9, 12, and 24 hours following administration of Bup-IR using MS. Bup-ER and Bup-IR levels were consistent among sexes of a given strain but varied between strains. Skin reactions, body weight loss, and histopathologic changes were greater in the Bup-ER-treated mice with some sex and strain differences. Due to changes found on histopathology of the skin sections taken from the injection site for Bup-ER-inoculated mice, a separate study to determine cytokine release following Bup-ER injection was performed and revealed only minor changes in a few cytokines. In conclusion, Bup-ER provided longer duration analgesia (>1 ng/mL) compared with Bup-IR. Based on differences found in the strains of mice evaluated, we recommend performing pharmacokinetic analyses for a given strain to determine the best dosing frequency and dose of buprenorphine (IR or ER) for procedures that require analgesia.

丁丙诺啡缓释和速释制剂在不同品系和性别小鼠体内的药动学和注射部位损伤评价。
丁丙诺啡是实验室啮齿类动物治疗中度至重度疼痛的常用镇痛药。我们评估了一种丁丙诺啡速释制剂(Bup-IR)和一种缓释制剂(Bup-ER)在4种不同的小鼠(C57BL/6、CD-1、BALB/c和CB17 SCID)两性中的药代动力学特性,这些小鼠通常用于我院皮肤病学和肿瘤学研究。接种后7天对注射部位的皮肤进行评估,并对反应进行评分,然后收集皮肤进行组织病理学分析。接种后1天和4天测定体重。我们假设与单剂量Bup-IR相比,给予Bup-ER可以提供更长的血药浓度持续时间(最低镇痛阈值)。我们分析了Bup-IR (0.3 mg/kg)和Bup-ER (1 mg/kg)的标准剂量,以及在Bup-ER给药后1、4、24、48、72和96小时以及在Bup-IR给药后0.25、0.5、1、2、3、6、9、12和24小时采集血液的生理盐水载体,使用ms分析了Bup-ER和Bup-IR水平在给定菌株的性别之间是一致的,但在菌株之间是不同的。bup - er治疗组小鼠的皮肤反应、体重减轻和组织病理学变化更大,存在一些性别和品系差异。由于从注射部位接种Bup-ER的小鼠皮肤切片的组织病理学变化,进行了一项单独的研究,以确定Bup-ER注射后的细胞因子释放,结果显示只有少数细胞因子发生了微小变化。综上所述,与Bup-IR相比,Bup-ER的镇痛持续时间更长(>.1 ng/mL)。根据评估小鼠品系的差异,我们建议对给定品系进行药代动力学分析,以确定需要镇痛的丁丙诺啡(IR或ER)的最佳给药频率和剂量。
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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