大鼠植入丁丙诺啡脂质体的长期研究。

Michael Guarnieri, Cory Brayton, Betty M Tyler
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引用次数: 2

摘要

研究阿片类药物的动物模型越来越引起人们的兴趣。我们已经在Fischer F344/NTac大鼠中检查了丁丙诺啡植入物的短期安全性,该大鼠接受了过量丁丙诺菲的胆固醇甘油三酯悬浮液的治疗。单次注射0.65 mg/kg可在3天内提供临床显著的血液镇痛水平。过量2至10倍剂量的药物脂质悬浮液的化学、血液学、凝血和尿液分析值均在正常范围内。组织病理学检查结果并不显著。药物注射周围的皮肤和下层组织并不明显。在此,我们报告了对注射0.65和1.3的雌性大鼠的长期随访研究结果 mg/kg。14个月的评估显示,没有发现可归因于药物或脂质悬浮液的异常结果。这些结果证实了胆固醇-甘油三酯载体系统在实验室动物皮下给药的安全性,并表明该模型可用于研究阿片类药物治疗的长期效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Long-Term Study of a Lipid-Buprenorphine Implant in Rats.

Animal models to study opiates are of growing interest. We have examined the short-term safety of buprenorphine implants in Fischer F344/NTac rats treated with excess doses of a cholesterol-triglyceride suspension of buprenorphine. A single injection of 0.65 mg/kg afforded clinically significant blood levels of analgesia for 3 days. Chemistry, hematology, coagulation, and urinalysis values with 2- to 10-fold excess doses of the drug-lipid suspension were within normal limits. Histopathology findings were unremarkable. The skin and underlying tissue surrounding the drug injection were unremarkable. Here we report the results of a long-term follow-up study of female rats injected with 0.65 and 1.3 mg/kg. The 14-month evaluation showed no abnormal findings that could be attributed to the drug or lipid suspension. These results confirm the safety of cholesterol-triglyceride carrier systems for subcutaneous drug delivery in laboratory animals and suggest that this model may be used to study long-term effects of opiate therapy.

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