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评价和比较两种常见绒猴(Callithrix jacchus)中丁丙诺啡控释制剂的药代动力学特征和安全性。

Evaluation and comparison of pharmacokinetic profiles and safety of two extended-release buprenorphine formulations in common marmosets (Callithrix jacchus).

机构信息

Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA, USA.

Department of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, UT, USA.

出版信息

Sci Rep. 2023 Jul 22;13(1):11864. doi: 10.1038/s41598-023-38973-2.

Abstract

While sustained-release buprenorphine (BSR) is used as a long-lasting opioid analgesic in common marmosets (Callithrix jacchus), there are no published studies on pharmaceutical-grade extended-release buprenorphine options such as Ethiqa XR (EXR) for this species. However, BSR is a compounded product and has been reported to cause injection site reactions in multiple species, including marmosets. Additionally, now with the availability of EXR, a pharmaceutical-grade veterinary product, the use of BSR in laboratory animals is not compliant with the Guide for the Care and Use of Laboratory Animals (Guide) unless scientifically justified and approved by the IACUC. We compared pharmacokinetic and safety profiles of BSR (0.15 mg/kg) and EXR (0.1-0.2 mg/kg) administered subcutaneously to adult marmosets. Blood was collected by venipuncture of the saphenous vein at multiple time points (0.25-72 h) and analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). EXR between 0.1 and 0.2 mg/kg resulted in a dose-dependent increase in C (1.43-2.51 ng/mL) and were not statistically different from BSR (1.82 ng/mL). T, lambda, and t were not statistically different between formulations. Mean plasma buprenorphine concentrations for BSR and EXR exceeded the therapeutic threshold (0.1 ng/mL) within 0.25 h and lasted for > 72 h. Mild sedation, but neither respiratory depression nor ataxia, was observed for both formulations. BSR injection sites had significantly higher histopathological scores compared to EXR. Video recordings for monitoring drug-induced behavioral changes showed increased animal activity levels after BSR and EXR versus saline controls. Norbuprenorphine, a buprenorphine metabolite associated with respiratory depression, was detected in the plasma after BSR and EXR administration as well as by in vitro liver microsome assays. In conclusion, we recommend using EXR over BSR as a long-lasting buprenorphine analgesic in marmosets because EXR is a pharmaceutical-grade formulation that is compliant with FDA guidelines and the Guide as well as exhibits comparable PK and safety profiles as BSR.

摘要

虽然缓释丁丙诺啡(BSR)被用作普通狨猴(Callithrix jacchus)的长效阿片类镇痛药,但尚无关于此类药物的医药级缓释丁丙诺啡(如 Ethiqa XR,EXR)的研究报告。然而,BSR 是一种复合产品,据报道会引起多种物种(包括狨猴)的注射部位反应。此外,现在有了医药级兽医产品 EXR,BSR 在实验动物中的使用不再符合《实验室动物护理和使用指南》(Guide)的规定,除非经过科学论证并得到 IACUC 的批准。我们比较了皮下给予成年狨猴 BSR(0.15mg/kg)和 EXR(0.1-0.2mg/kg)的药代动力学和安全性特征。通过静脉穿刺采集 saphenous 静脉的血液,在多个时间点(0.25-72h)采集并通过液相色谱-串联质谱法(LC-MS/MS)进行分析。0.1-0.2mg/kg 的 EXR 导致 C(1.43-2.51ng/mL)呈剂量依赖性增加,与 BSR(1.82ng/mL)无统计学差异。两种制剂的 T、lambda 和 t 无统计学差异。BSR 和 EXR 的平均血浆丁丙诺啡浓度在 0.25h 内超过治疗阈值(0.1ng/mL),并持续超过 72h。两种制剂均观察到轻度镇静,但无呼吸抑制或共济失调。BSR 注射部位的组织病理学评分明显高于 EXR。用于监测药物引起的行为变化的视频记录显示,BSR 和 EXR 给药后动物活动水平增加,而与生理盐水对照相比。诺布丁诺啡,一种与呼吸抑制相关的丁丙诺啡代谢物,在 BSR 和 EXR 给药后以及在体外肝微粒体测定中均有检测到。总之,我们建议在狨猴中使用 EXR 替代 BSR 作为长效丁丙诺啡镇痛药,因为 EXR 是一种医药级制剂,符合 FDA 指南和《指南》的规定,并且与 BSR 具有相似的 PK 和安全性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2340/10363172/ce449489d105/41598_2023_38973_Fig1_HTML.jpg

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