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新型细胞因子标志物可用于使用重建人体表皮模型的医疗器械皮肤刺激测试。

Novel cytokine marker available for skin irritation testing of medical devices using reconstructed human epidermis models.

机构信息

Division of Medical Devices, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-9501, Japan.

Division of Medical Devices, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-9501, Japan.

出版信息

Toxicol In Vitro. 2020 Oct;68:104919. doi: 10.1016/j.tiv.2020.104919. Epub 2020 Jul 6.

Abstract

In biological safety evaluation of medical devices, false-negative results have been observed during skin irritation testing using the reconstructed human epidermis (RhE) model when measuring cell viability as a single marker. Therefore, to improve testing accuracy, this study conducted a comprehensive survey and performance evaluation of cytokines to identify a second marker. In addition to IL-1α, macrophage migration inhibitory factor (MIF) was newly identified as a candidate marker, in the Bio-Plex assay of EpiDerm model exposed to polymer sample extracts. Irritation based on cell viability level was not accurately determined in LabCyte model using silicone spiked with 25% heptanoic acid (HA). By contrast, the irritation potency was accurately assessed in detail by measuring IL-1α or MIF. Further, IL-1α and MIF levels in EpiDerm, LabCyte, and EpiSkin models stimulated with sodium dodecyl sulfate (SDS) were inversely correlated with cell viability, and were detected even at low SDS concentrations without cell toxicity. Additionally, MIF demonstrated greater S/N ratio and dose-dependency at high SDS concentrations in some models compared to IL-1α. These results indicated that MIF might be a useful second marker for improving the sensitivity and accuracy of skin irritation testing with RhE models.

摘要

在医疗器械的生物安全评价中,使用重建人表皮(RhE)模型进行皮肤刺激测试时,当将细胞活力作为单一标志物进行测量时,观察到假阴性结果。因此,为了提高测试准确性,本研究对细胞因子进行了全面调查和性能评估,以确定第二个标志物。除了 IL-1α,新鉴定出巨噬细胞移动抑制因子(MIF)是暴露于聚合物样品提取物的 EpiDerm 模型中的生物素标记物候选标志物。在使用 25%庚酸(HA)掺杂的硅酮的 LabCyte 模型中,基于细胞活力水平的刺激不能准确确定。相比之下,通过测量 IL-1α或 MIF 可以准确评估刺激强度。此外,用十二烷基硫酸钠(SDS)刺激的 EpiDerm、LabCyte 和 EpiSkin 模型中的 IL-1α和 MIF 水平与细胞活力呈负相关,并且在没有细胞毒性的低 SDS 浓度下也可以检测到。此外,与 IL-1α相比,MIF 在一些模型中在高 SDS 浓度下显示出更大的 S/N 比和剂量依赖性。这些结果表明,MIF 可能是提高 RhE 模型皮肤刺激测试灵敏度和准确性的有用的第二个标志物。

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