Park Se Yeon, Koh Won-Gun, Lee Hyun Jong
School of Chemical, Biological and Battery Engineering, Gachon University, 1342 Seongnam-daero, Seongnam-si, Gyeonggi-do 13120, Republic of Korea.
Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea.
Eur J Pharm Biopharm. 2024 Sep;202:114417. doi: 10.1016/j.ejpb.2024.114417. Epub 2024 Jul 14.
Conventional 2D drug screening often fails to accurately predict clinical outcomes. We present an innovative approach to improve hepatotoxicity assessment by encapsulating HepG2 spheroids in gelatin hydrogel matrices with different mechanical properties. Encapsulated spheroids exhibit sustained liver-specific functionality, enhanced expression of drug-metabolizing enzymes, and increased drug sensitivity compared to 2D cultures. The platform detects critical variations in drug response, with significant differences in IC values between 2D and spheroid cultures ranging from 1.3-fold to > 13-fold, particularly for acetaminophen. Furthermore, drug-metabolizing enzyme expression varies across hydrogel concentrations, suggesting a role for matrix mechanical properties in modulating hepatocyte function. This novel spheroid-hydrogel platform offers a transformative approach to hepatotoxicity assessment, providing increased sensitivity, improved prediction, and a more physiologically relevant environment. The use of such advanced in vitro models can accelerate drug development, reduce animal testing, and contribute to improved patient safety and clinical outcomes.
传统的二维药物筛选往往无法准确预测临床结果。我们提出了一种创新方法,通过将HepG2球体封装在具有不同机械性能的明胶水凝胶基质中来改进肝毒性评估。与二维培养相比,封装的球体表现出持续的肝脏特异性功能、药物代谢酶表达增强以及药物敏感性增加。该平台可检测药物反应中的关键差异,二维和球体培养之间的IC值存在显著差异,范围从1.3倍到>13倍,对乙酰氨基酚尤为明显。此外,药物代谢酶表达随水凝胶浓度而变化,表明基质机械性能在调节肝细胞功能中起作用。这种新型的球体-水凝胶平台为肝毒性评估提供了一种变革性方法,具有更高的灵敏度、更好的预测性以及更具生理相关性的环境。使用这种先进的体外模型可以加速药物开发,减少动物试验,并有助于提高患者安全性和临床结果。