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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Intralaboratory and interlaboratory evaluation of the EpiDerm 3D human reconstructed skin micronucleus (RSMN) assay.
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Intralaboratory and interlaboratory evaluation of the EpiDerm 3D human reconstructed skin micronucleus (RSMN) assay.

机译:EpiDerm 3D人体重建皮肤微核(RSMN)分析的实验室内和实验室间评估。

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摘要

A novel in vitro human reconstructed skin micronucleus (RSMN) assay has been developed using the EpiDerm 3D human skin model [R. D. Curren, G. C. Mun, D. P. Gibson, and M. J. Aardema, Development of a method for assessing micronucleus induction in a 3D human skin model EpiDerm, Mutat. Res. 607 (2006) 192-204]. The RSMN assay has potential use in genotoxicity assessments as a replacement for in vivo genotoxicity assays that will be banned starting in 2009 according to the EU 7th Amendment to the Cosmetics Directive. Utilizing EpiDerm tissues reconstructed with cells from four different donors, intralaboratory and interlaboratory reproducibility of the RSMN assay were examined. Seven chemicals were evaluated in three laboratories using a standard protocol. Each chemical was evaluated in at least two laboratories and in EpiDerm tissues from at least two different donors. Three model genotoxins, mitomycin C (MMC), vinblastine sulfate (VB) and methyl methanesulfonate (MMS) induced significant, dose-related increases in cytotoxicity and MN induction in EpiDerm tissues. Conversely, four dermal non-carcinogens, 4-nitrophenol (4-NP), trichloroethylene (TCE), 2-ethyl-1,3-hexanediol (EHD), and 1,2-epoxydodecane (EDD) were negative in the RSMN assay. Results between tissues reconstructed from different donors were comparable. These results indicate the RSMN assay using the EpiDerm 3D human skin model is a promising new in vitro genotoxicity assay that allows evaluation of chromosome damage following "in vivo-like" dermal exposures.
机译:已使用EpiDerm 3D人体皮肤模型开发了一种新型的体外人体重建皮肤微核(RSMN)分析。 D.Curren,G.C.Mun,D.P.Gibson和M.J.Aardema,评估3D人皮肤模型EpiDerm的微核诱导方法的开发,Mutat。 Res。 607(2006)192-204]。根据欧盟《化妆品指令第7修正案》,自2009年起将禁止在体内进行基因遗传毒性测定,因此RSMN测定法在遗传毒性评估中具有潜在的用途。利用来自四个不同供体的细胞重建的EpiDerm组织,检查了实验室内和实验室间RSMN测定的可重复性。使用标准协议,在三个实验室中对七种化学品进行了评估。至少在两个实验室和至少两个不同供体的EpiDerm组织中对每种化学品进行了评估。三种模型基因毒素,丝裂霉素C(MMC),硫酸长春碱(VB)和甲磺酸甲酯(MMS)在EpiDerm组织中诱导了明显的剂量相关的细胞毒性和MN诱导。相反,四种皮肤非致癌物,4-硝基苯酚(4-NP),三氯乙烯(TCE),2-乙基-1,3-己二醇(EHD)和1,2-环氧十二烷(EDD)呈阴性。 。从不同供体重建的组织之间的结果具有可比性。这些结果表明,使用EpiDerm 3D人体皮肤模型进行的RSMN测定是一种很有前途的新的体外遗传毒性测定,它可以评估“体内样”皮肤暴露后的染色体损伤。

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