Fernandez-Carro Estibaliz, Angenent Maricke, Gracia-Cazaña Tamara, Gilaberte Yolanda, Alcaine Clara, Ciriza Jesús
Tissue Microenvironment (TME) Lab, Aragón Institute of Engineering Research (I3A), University of Zaragoza, 50018 Zaragoza, Spain.
Department of Dermatology, University Hospital Miguel Servet, IIS Aragón, 50018 Zaragoza, Spain.
Pharmaceutics. 2022 Jul 6;14(7):1417. doi: 10.3390/pharmaceutics14071417.
Preclinical research remains hampered by an inadequate representation of human tissue environments which results in inaccurate predictions of a drug candidate's effects and target's suitability. While human 2D and 3D cell cultures and organoids have been extensively improved to mimic the precise structure and function of human tissues, major challenges persist since only few of these models adequately represent the complexity of human tissues. The development of skin-on-chip technology has allowed the transition from static 3D cultures to dynamic 3D cultures resembling human physiology. The integration of vasculature, immune system, or the resident microbiome in the next generation of SoC, with continuous detection of changes in metabolism, would potentially overcome the current limitations, providing reliable and robust results and mimicking the complex human skin. This review aims to provide an overview of the biological skin constituents and mechanical requirements that should be incorporated in a human skin-on-chip, permitting pharmacological, toxicological, and cosmetic tests closer to reality.
临床前研究仍然受到人类组织环境代表性不足的阻碍,这导致对候选药物的效果和靶点适用性的预测不准确。虽然人类二维和三维细胞培养以及类器官已经得到了广泛改进,以模拟人类组织的精确结构和功能,但主要挑战依然存在,因为这些模型中只有少数能够充分体现人类组织的复杂性。芯片上皮肤技术的发展使得从静态三维培养向类似人体生理学的动态三维培养转变成为可能。在下一代芯片上皮肤中整合脉管系统、免疫系统或常驻微生物群,并持续检测代谢变化,可能会克服当前的局限性,提供可靠且稳健的结果,并模拟复杂的人类皮肤。本综述旨在概述应纳入人类芯片上皮肤的生物皮肤成分和机械要求,以便进行更贴近实际的药理学、毒理学和化妆品测试。