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首页> 外文期刊>Alternatives to laboratory animals: ATLA >Further verification of an in vitro tier system for the identification of cosmetic ingredients that are not ocular irritants.
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Further verification of an in vitro tier system for the identification of cosmetic ingredients that are not ocular irritants.

机译:用于鉴定不是眼刺激性化妆品成分的体外分级系统的进一步验证。

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A tier evaluation system for the identification of cosmetic ingredients that are not ocular irritants was applied to 59 cosmetic ingredients, for which in vivo data were available. The tier system employs monolayer cultures of SIRC cells, an established cell line originally derived from rabbit cornea, and a threedimensional living dermal model (LDM; MATREX(TM)), which consists of human dermal fibroblasts in a contracted collagen lattice. The effects of ingredients on monolayer cultures of SIRC cells were determined by Crystal Violet staining (in the SIRC-CVS assay), and the effects on the LDM were measured by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (in the LDM-MTT assay). The classifications of eye irritancy predicted by the in vitro system were compared with previously reported data obtained with the in vivo Draize rabbit eye test. The in vivo classification was based on appearance of corneal damage, or a maximal average score (MAS) of 15 as the cut-off point. The SIRC-CVS assay was effective in the prediction of compounds that would be non-irritants at a concentration of 10%, while the subsequent LDM-MTT assay could predict non-irritancy at various lower and higher concentrations, including 10%. The tier system gave very few false-negative predictions, though false positives were unavoidable. Performing the LDM-MTT assay with an additional 73 ingredients gave similar results in the prediction of non-irritancy at various concentrations. Our findings indicate that the tier system may be suitable for the safety assessment of eye irritancy of ingredients intended to be used in cosmetics and medicated cosmetics in Japan.
机译:将用于鉴定不是眼刺激物的化妆品成分的分级评估系统应用于59种化妆品成分,可获得体内数据。分层系统采用单层培养的SIRC细胞,最初源自兔角膜的已建立细胞系以及三维活体真皮模型(LDM; MATREX™),该模型由处于收缩胶原蛋白晶格中的人真皮成纤维细胞组成。通过结晶紫染色(在SIRC-CVS分析中)确定成分对SIRC细胞单层培养的影响,并通过使用3-(4,5-二甲基噻唑-2-基)-2测定对LDM的影响,5-二苯基溴化四氮唑(在LDM-MTT分析中)。将体外系统预测的眼睛刺激性分类与体内Draize兔眼测试获得的先前报道数据进行了比较。体内分类基于角膜损伤的出现或最高平均分(MAS)15作为分界点。 SIRC-CVS分析可有效预测浓度为10%的非刺激性化合物,而随后的LDM-MTT分析则可预测各种较低和较高浓度(包括10%)的非刺激性。尽管不可避免地会出现误报,但层级系统很少给出假阴性预测。用其他73种成分进行LDM-MTT分析得出的预测在各种浓度下无刺激性的结果相似。我们的研究结果表明,该分级系统可能适合用于日本化妆品和药用化妆品中成分对眼睛刺激性的安全性评估。

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