首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >An In Vitro Skin Irritation Test (SIT) using the EpiDerm Reconstructed Human Epidermal (RHE) Model
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An In Vitro Skin Irritation Test (SIT) using the EpiDerm Reconstructed Human Epidermal (RHE) Model

机译:使用EpiDerm重建的人类表皮(RHE)模型进行的体外皮肤刺激试验(SIT)

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摘要

The EpiDerm Skin Irritation test (EpiDerm SIT) was developed (1,2,3) and validated (4,5) for in vitro skin irritation testing of chemicals, including cosmetic and pharmaceutical ingredients. The EpiDerm SIT utilizes the 3D in vitro reconstructed human epidermal (RHE) model EpiDerm. The procedure described in this protocol allows for discrimination between irritants of GHS category 2 and non-irritants (6). The test is performed over the course of a 4 day time period, consisting of pre-incubation, 60 minute exposure, 42 hour post-incubation and MTT viability assay. After tissue receipt and overnight pre-incubation (Day 0), tissues are topically exposed to the test chemicals (Day 1), which can be liquid, semi-solids, solid or wax. Three tissues are used for each test chemical, as well as for the positive control (5% aq. SDS solution), and a negative control (DPBS). Chemical exposure lasts for 60 minutes, 35 min of which the tissues are kept in an incubator at 37°C. The test substances are then removed from the tissue surface by an extensive washing procedure. The tissue inserts are blotted and transferred to fresh medium. After a 24 hr incubation period (Day 2), the medium is exchanged. The medium can be saved for further analysis of cytokines or other endpoints of interest. After the medium exchange, tissues are incubated for an additional 18 hours. At the end of the entire 42h post-incubation (day 3), the tissues are transferred into yellow MTT solution and incubated for 3 hours. The resultant purple-blue formazan salt, formed mainly by mitochondrial metabolism, is extracted for 2 hours using isopropanol. The optical density of the extracted formazan is determined using a spectrophotometer. A chemical is classified as an irritant if the tissue viability relative to the negative control treated tissues is reduced below 50%. This procedure can be used as full replacement of the in vivo rabbit skin irritation test for hazard identification and labeling of chemicals in line with EU regulations (7).
机译:开发了(1,2,3)的EpiDerm皮肤刺激测试(EpiDerm SIT),并通过了(4,5)验证,可用于化学药品(包括化妆品)的体外皮肤刺激测试和药物成分。 EpiDerm SIT利用3D体外重建的人类表皮(RHE)模型EpiDerm。该协议中描述的过程允许区分GHS第2类刺激物和非刺激性(6)。该测试在为期4天的过程中执行,包括预培养,60分钟暴露,培养后42小时和MTT活力测定。接受组织并进行过夜预培养(第0天)后,将组织局部暴露于测试化学物质(第1天),这些化学物质可以是液体,半固体,固体或蜡。每种测试化学品以及阳性对照(5%SDS水溶液)和阴性对照(DPBS)使用三个组织。化学暴露持续60分钟,其中35分钟将组织置于37°C的恒温箱中。然后通过大量清洗程序从组织表面除去测试物质。组织插入物被吸干并转移到新鲜培养基中。孵育24小时后(第2天),更换培养基。可以保存培养基,以进一步分析细胞因子或其他感兴趣的终点。更换培养基后,将组织再孵育18小时。在整个孵育后42小时(第3天)结束时,将组织转移到黄色MTT溶液中并孵育3小时。使用异丙醇将所得的主要由线粒体代谢形成的紫蓝色甲maz盐萃取2小时。使用分光光度计确定提取的甲maz的光密度。如果组织相对于阴性对照治疗的组织的生存力降低到50%以下,则将其分类为刺激物。该程序可完全替代体内兔子皮肤刺激性测试,以符合欧盟法规(7)进行危害识别和化学标签。

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