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肝脏器官芯片在成药性评价中的应用进展

Application of liver-on-a-chip in druggability evaluation

  • 摘要: 成药性评价是新药研发的核心环节,而现有体外肝脏模型的预测准确性低与成本高昂,是制约该环节的关键瓶颈。因此,制药行业愈发需要可靠的肝脏体外模型以提高新药研发效率。由于传统动物模型和体外2D培养模型在模拟体内生理和病理上存在着局限性,近年来,借助微流控技术、体外细胞培养技术和生物传感技术的进步,肝脏器官芯片(liver-on-a-chip, LOC)在新药研发领域日益得到关注,有望成为解决成药性评价痛点的有力武器。本文在介绍肝脏器官芯片构建技术的基础上,着重从疾病模型构建、药物代谢研究和药物安全性评价等角度总结现有肝脏器官芯片的研究和应用,分析其在成药性评价中起到的作用,并探讨该领域当前面临的挑战与未来展望。

     

    Abstract: Druggability evaluation is one of the core processes in new drug development, yet the inaccuracy and high cost of existing in vitro liver models have been a major technical bottleneck, leading to an increasing demand from the pharmaceutical industry for reliable in vitro liver models to enhance the efficiency of new drug research and development. Traditional animal models and in vitro 2D culture models have their limitations in simulating in vivo physiological and pathological conditions, making it challenging to accurately predict drug efficacy and safety. With the advancement of microfluidic technology, in vitro cell culture, and biosensor technology, liver-on-a-chip (LOC) has garnered increasing attention in the field of new drug development in recent years, and is expected to become a powerful tool for addressing the challenges in druggability evaluation. While introducing the construction technology of LOC, this article mainly summarizes the research and application of existing LOC from the perspectives of disease model construction, drug metabolism research, and drug safety evaluation. Furthermore, it analyzes the role of LOC in druggability evaluation and discusses the current challenges and prospects in this field.

     

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