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叠氮化钠不太适合作为体外克隆形成试验中药物诱导致死率的阳性对照。

Sodium azide is less suitable as a positive control of drug-induced lethality for in vitro clonogenic assays.

作者信息

Lelieveld P, Aapro M S, van Lambalgen R, van den Berg K J

出版信息

Invest New Drugs. 1986;4(4):367-71. doi: 10.1007/BF00173509.

DOI:10.1007/BF00173509
PMID:3583644
Abstract

Sodium azide (6 mg/ml) was used as a positive control for drug-induced lethality in an in vitro clonogenic assay. Petri dishes containing control and sodium azide treated cultures of WiDr cells were placed together in a large Petri dish and incubated at 37 degrees C in an atmosphere of 10% CO2 in air. No growth was observed. Control cells formed colonies only when the dishes were separated from the sodium azide dishes. Using a microtiter plate the toxic effect was inversely related to the distance of the test cultures from the sodium azide treated cultures. These results suggested the formation of a toxic gas or vapour from sodium azide under cell culture conditions, probably an azide. Chemical analysis was based on characteristic reactions, such as the production of a precipitate with silver ions or formation of a red-coloured complex with ferric salts. On a microtiter plate, a gradient of the expected precipitate or red colour was observed, the highest amounts adjacent to the wells containing sodium azide. These results show that sodium azide acts as a positive control of drug-induced lethality for in vitro clonogenic assays. However, the formation of a highly toxic vapour, most likely hydrazaic acid, makes it a less suitable standard.

摘要

叠氮化钠(6毫克/毫升)在体外克隆形成试验中用作药物诱导致死性的阳性对照。将含有WiDr细胞对照培养物和经叠氮化钠处理的培养物的培养皿一起放置在一个大培养皿中,并在37摄氏度、含10%二氧化碳的空气环境中孵育。未观察到生长。只有当培养皿与叠氮化钠培养皿分开时,对照细胞才形成菌落。使用微量滴定板时,毒性作用与测试培养物与经叠氮化钠处理的培养物之间的距离呈负相关。这些结果表明,在细胞培养条件下,叠氮化钠会形成一种有毒气体或蒸气,可能是一种叠氮化物。化学分析基于特征反应,例如与银离子产生沉淀或与铁盐形成红色络合物。在微量滴定板上,观察到预期沉淀或红色的梯度,最高量出现在含有叠氮化钠的孔附近。这些结果表明,叠氮化钠在体外克隆形成试验中可作为药物诱导致死性的阳性对照。然而,形成一种剧毒蒸气,很可能是氢叠氮酸,使其不太适合作为标准物质。

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Reduced cell viability in vitro following exposure to a routine laboratory disinfectant. A cautionary note.暴露于常规实验室消毒剂后体外细胞活力降低。一则警示。

本文引用的文献

1
Usefulness of abrin as a positive control for the human tumor clonogenic assay.相思子毒素作为人类肿瘤克隆形成试验阳性对照的效用。
Invest New Drugs. 1983;1(4):277-81. doi: 10.1007/BF00177410.
2
Development of a miniaturized, improved nucleic acid precursor incorporation assay for chemosensitivity testing of human solid tumors.开发一种用于人类实体瘤化学敏感性测试的小型化、改进的核酸前体掺入测定法。
Cancer Res. 1985 Nov;45(11 Pt 1):5436-41.
3
Application of a human tumor colony-forming assay to new drug screening.人肿瘤集落形成试验在新药筛选中的应用。
Cytotechnology. 1990 Sep;4(2):109-10. doi: 10.1007/BF00365090.
Cancer Res. 1985 May;45(5):2145-53.
4
Characterization of the WIDR: a human colon carcinoma cell line.WIDR的特性:一种人结肠癌细胞系。
In Vitro. 1979 Jun;15(6):401-8. doi: 10.1007/BF02618407.