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在实验动物环境中多剂量瓶中稀释卡洛芬的无菌性和稳定性

Sterility and Stability of Diluted Carprofen in a Multidose Vial in the Laboratory Animal Setting.

作者信息

Simonek Gregory D, Alarcio Gwendolyne G, Brignolo Laurie L

机构信息

School of Veterinary Medicine, University of California, Davis, California;, Email:

California Animal Health and Food Safety Laboratory System, University of California, Davis, California.

出版信息

J Am Assoc Lab Anim Sci. 2017 May 1;56(3):296-298.

Abstract

Using compounded multidose vials (cMDV) is a common practice in the laboratory animal setting, where medications often are diluted to provide appropriate doses to rodents. However, bacterial contamination of MDV has been well established in both the human and veterinary medical literature. For this study, we created 14 cMDV by diluting carprofen into sterile water (dilution, 1:10) and stored 6 cMDV each at 5 and 24 °C. The stoppers of the cMDV were not cleaned with alcohol, and all were punctured twice daily for 28 d. The sterility of the diluted carprofen was evaluated by assessing bacterial growth on days 0, 7, 14, 21, and 28 and by testing for bacterial endotoxin on days 0 and 28. We used liquid chromatography-tandem mass spectrometry to assess the stability of 2 cMDV, with each cMDV being divided into the 2 storage-temperature subsets for days 0, 7, 14, 21, and 28. Neither bacterial contamination nor endotoxin was detected, and drug stability was stable over the 28 d. We suggest that with pragmatic techniques, such as secondary containment and consistent use of new needles, the contents of cMDV can remain sterile and stable for 28 d.

摘要

在实验动物环境中,使用复合多剂量瓶(cMDV)是一种常见做法,在这种环境中,药物通常会被稀释以给啮齿动物提供合适的剂量。然而,人类和兽医学文献中均已明确证实多剂量瓶存在细菌污染问题。在本研究中,我们通过将卡洛芬稀释于无菌水中(稀释比例为1:10)制备了14个cMDV,并分别在5℃和24℃下各储存6个cMDV。cMDV的瓶塞未用酒精清洁,所有瓶子每天穿刺两次,持续28天。通过评估第0、7、14、21和28天的细菌生长情况以及检测第0天和第28天的细菌内毒素来评估稀释后卡洛芬的无菌性。我们使用液相色谱 - 串联质谱法评估2个cMDV的稳定性,每个cMDV在第0、7、14、21和28天被分为两个储存温度组。未检测到细菌污染和内毒素,并且药物稳定性在28天内保持稳定。我们建议,采用诸如二级防护和持续使用新针头之类的实用技术,cMDV的内容物可在28天内保持无菌和稳定。

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