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ECVAM retrospective validation of in vitro micronucleus test (MNT)

机译:ECVAM体外微核试验(MNT)的回顾性验证

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摘要

In the past decade several studies comparing the in vitro chromosome aberration test (CAT) and the in vitro micronucleus test (MNT) were performed. A high correlation was observed in each of the studies (>85%); however, no formal validation for the micronucleus in vitro assay had been carried out. Therefore, a working group was established by the European Centre for the Validation of Alternative Methods (ECVAM) to perform a retrospective validation of the existing data, in order to evaluate the validity of the in vitro MNT on the basis of the modular validation approach. The primary focus of this retrospective validation was on the evaluation of the potential of the in vitro MNT as alternative to the standard in vitro CAT. The working group evaluated, in a first step, the available published data and came to the conclusion that two studies [German ring trial, von der Hude, W., Kalweit, S., Engelhardt, G. et al. (2000) In-vitro micronucleus assay with Chinese hamster V79 cells: results of a collaborative study with 26 chemicals. Mutat. Res., 468, 137–163, and SFTG International Collaborative Study, Lorge, E., Thybaud, V., Aardema, M., Oliver, J., Wataka, A., Lorenzon, G. and Marzin, D. (2006) SFTG International Collaborative Study on in-vitro micronucleus test I. General conditions and overall conclusions of the study. Mutat. Res., 607, 13–36] met the criteria for a retrospective validation according to the criteria previously defined by the working group. These two studies were evaluated in depth (including the reanalysis of raw data) and provided the information required for assessing the reliability (reproducibility) of the test. For the assessment of the concordance between the in vitro MNT and the in vitro CAT, additional published data were considered. Based on this retrospective validation, the ECVAM Validation Management Team concluded that the in vitro MNT is reliable and relevant and can therefore be used as an alternative method to the in vitro CAT. Following peer review, these conclusions were formally endorsed by the ECVAM Scientific Advisory Committee.
机译:在过去的十年中,进行了一些比较体外染色体畸变测试(CAT)和体外微核测试(MNT)的研究。在每个研究中均观察到高度相关性(> 85%);但是,尚未对微核体外测定法进行正式验证。因此,欧洲替代方法验证中心(ECVAM)成立了一个工作组,对现有数据进行回顾性验证,以便在模块化验证方法的基础上评估体外MNT的有效性。回顾性验证的主要重点是评估体外MNT替代标准体外CAT的潜力。工作组首先评估了可用的公开数据,得出的结论是,两项研究[德国环试验,冯·德·胡德(W. der der Hude),卡尔维特(S.),恩格哈特(Engelhardt)等。 (2000)用中国仓鼠V79细胞进行体外微核分析:与26种化学物质合作研究的结果。笨蛋Res。,468,137–163,和SFTG国际合作研究,Lorge,E.,Thybaud,V.,Aardema,M.,Oliver,J.,Wataka,A.,Lorenzon,G.和Marzin,D.( 2006)SFTG体外微核试验国际合作研究I.研究的一般条件和总体结论。笨蛋[Res。,607,13–36]符合根据工作组先前定义的标准进行追溯验证的标准。对这两项研究进行了深入评估(包括对原始数据的重新分析),并提供了评估测试可靠性(可重复性)所需的信息。为了评估体外MNT和体外CAT之间的一致性,考虑了其他已公开的数据。基于此回顾性验证,ECVAM验证管理团队得出结论,体外MNT是可靠且相关的,因此可以用作体外CAT的替代方法。经过同行评审,这些结论得到ECVAM科学咨询委员会的正式认可。

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