Subcutaneous Implants of Buprenorphine-Cholesterol-Triglyceride Powder in Mice.

Journal of veterinary medicine Pub Date : 2014-01-01 Epub Date: 2014-11-27 DOI:10.1155/2014/365673
L DeTolla, R Sanchez, E Khan, B Tyler, M Guarnieri
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引用次数: 6

Abstract

Subcutaneous drug implants are convenient systems for the long-term delivery of drugs in animals. Lipid carriers are logical tools because they generally allow for higher doses and low toxicity. The present study used an US Food and Drug Administration Target Animal Safety test system to evaluate the safety of a subcutaneous implant of a cholesterol-triglyceride-buprenorphine powder in 120 BALB/c mice. Mice were evaluated in 4- and 12-day trials with 1- and 5-fold doses of the intended 3 mg/kg dose of drug. One male mouse treated with three 3 mg/kg doses and surgery on days 0, 4, and 8 died on day 9. The cause of death was not determined. In the surviving 119 mice there was no evidence of skin reaction at the site of the implant. Compared to control animals treated with saline, weight measurements, clinical pathology, histopathology, and clinical observations were unremarkable. These results demonstrate that the lipid carrier is substantially safe. Cholesterol-triglyceride-drug powders may provide a valuable research tool for studies of analgesic and inflammatory drug implants in veterinary medicine.

Abstract Image

丁丙诺啡-胆固醇-甘油三酯粉末小鼠皮下植入。
皮下药物植入是动物体内长期给药的方便系统。脂质载体是合理的工具,因为它们通常允许更高的剂量和低毒性。本研究使用美国食品和药物管理局的靶动物安全测试系统来评估120只BALB/c小鼠皮下植入胆固醇-甘油三酯-丁丙诺啡粉末的安全性。小鼠在4天和12天的试验中被评估为1倍和5倍剂量的预期3mg /kg剂量的药物。1只雄性小鼠分别在第0、4和8天接受3次3 mg/kg剂量的治疗和手术,第9天死亡。死亡原因尚未确定。在存活的119只小鼠中,植入部位没有皮肤反应的迹象。与生理盐水治疗的对照组动物相比,体重测量、临床病理、组织病理学和临床观察均无显著差异。这些结果表明,脂质载体基本上是安全的。胆固醇-甘油三酯药物粉末可为兽药镇痛和消炎药植入物的研究提供有价值的研究工具。
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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