Rhee Stephen, Xia Chunguang, Chandra Aditya, Hamon Morgan, Lee Geonhui, Yang Chen, Guo Zaixun, Sun Bingjie
BMF Biotechnology, Inc., San Diego, CA 92121, USA.
BMF Nano Material Technology Co., Ltd., Shenzhen 518100, China.
Bioengineering (Basel). 2024 Oct 23;11(11):1055. doi: 10.3390/bioengineering11111055.
In this study, we present a novel 3D perfused skin-on-a-chip model fabricated using micro-precision 3D printing, which offers a streamlined and reproducible approach for incorporating perfusion. Perfused skin models are well-regarded for their advantages, such as improved nutrient supply, enhanced barrier function, and prolonged tissue viability. However, current models often require complex setups, such as self-assembled endothelial cells or sacrificial rods, which are prone to variability and time-consuming. Our model uses projection micro-stereolithography 3D printing to create precise microcapillary-like channels using a biocompatible resin, overcoming the drug-absorbing properties of PDMS. A customized chip holder allows for the simultaneous culture of six perfused chips, enabling high-throughput testing. The engineered skin-on-a-chip features distinct dermis and epidermis layers, confirmed via H&E staining and immunostaining. To evaluate drug screening capabilities, inflammation was induced using TNF-α and treated with dexamethasone, with cytokine levels compared to 2D cultures and human skin biopsies. Our 3D model exhibited drug response trends similar to human skin, while showing reduced cytotoxicity over time compared to biopsies. This perfused skin-on-a-chip provides a reliable, physiologically relevant alternative for drug and cosmetics screening, simplifying perfusion setup while preserving key benefits.
在本研究中,我们展示了一种使用微精密3D打印制造的新型3D灌注芯片皮肤模型,该模型为纳入灌注提供了一种简化且可重复的方法。灌注皮肤模型因其优点而备受关注,如改善营养供应、增强屏障功能和延长组织活力。然而,当前模型通常需要复杂的设置,如自组装内皮细胞或牺牲棒,这些方法容易出现变异性且耗时。我们的模型使用投影微立体光刻3D打印技术,用生物相容性树脂创建精确的微毛细血管样通道,克服了聚二甲基硅氧烷(PDMS)的药物吸收特性。定制的芯片支架允许同时培养六个灌注芯片,实现高通量测试。通过苏木精和伊红(H&E)染色及免疫染色证实,工程化的芯片皮肤具有不同的真皮和表皮层。为了评估药物筛选能力,使用肿瘤坏死因子-α(TNF-α)诱导炎症,并用地塞米松治疗,将细胞因子水平与二维培养和人体皮肤活检进行比较。我们的3D模型表现出与人体皮肤相似的药物反应趋势,同时与活检相比,随着时间的推移细胞毒性降低。这种灌注芯片皮肤为药物和化妆品筛选提供了一种可靠的、生理相关的替代方案,简化了灌注设置,同时保留了关键优势。