• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过将HepG2球体封装在明胶水凝胶基质中来增强肝毒性评估:弥合从二维到三维培养的差距。

Enhanced hepatotoxicity assessment through encapsulated HepG2 spheroids in gelatin hydrogel matrices: Bridging the gap from 2D to 3D culture.

作者信息

Park Se Yeon, Koh Won-Gun, Lee Hyun Jong

机构信息

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.

出版信息

Eur J Pharm Biopharm. 2024 Sep;202:114417. doi: 10.1016/j.ejpb.2024.114417. Epub 2024 Jul 14.

DOI:10.1016/j.ejpb.2024.114417
PMID:39013493
Abstract

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.

摘要

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。

相似文献

1
Enhanced hepatotoxicity assessment through encapsulated HepG2 spheroids in gelatin hydrogel matrices: Bridging the gap from 2D to 3D culture.通过将HepG2球体封装在明胶水凝胶基质中来增强肝毒性评估:弥合从二维到三维培养的差距。
Eur J Pharm Biopharm. 2024 Sep;202:114417. doi: 10.1016/j.ejpb.2024.114417. Epub 2024 Jul 14.
2
Integrated in vitro models for hepatic safety and metabolism: evaluation of a human Liver-Chip and liver spheroid.用于肝安全性和代谢的体外整合模型:人肝芯片和肝球体的评估。
Arch Toxicol. 2019 Apr;93(4):1021-1037. doi: 10.1007/s00204-019-02427-4. Epub 2019 Mar 26.
3
A 3D spheroid model of quadruple cell co-culture with improved liver functions for hepatotoxicity prediction.一种具有改善肝功能的四重细胞共培养 3D 球体模型,用于肝毒性预测。
Toxicology. 2024 Jun;505:153829. doi: 10.1016/j.tox.2024.153829. Epub 2024 May 11.
4
Effects of mechanical properties of gelatin methacryloyl hydrogels on encapsulated stem cell spheroids for 3D tissue engineering.甲基丙烯酰化明胶水凝胶的力学性能对用于三维组织工程的包封干细胞球状体的影响。
Int J Biol Macromol. 2022 Jan 1;194:903-913. doi: 10.1016/j.ijbiomac.2021.11.145. Epub 2021 Nov 25.
5
A sub-chronic Xysmalobium undulatum hepatotoxicity investigation in HepG2/C3A spheroid cultures compared to an in vivo model.亚慢性弯叶黑黄檀肝毒性在 HepG2/C3A 球体培养物中的研究与体内模型比较。
J Ethnopharmacol. 2019 Jul 15;239:111897. doi: 10.1016/j.jep.2019.111897. Epub 2019 Apr 19.
6
Evaluation of a Three-Dimensional Primary Human Hepatocyte Spheroid Model: Adoption and Industrialization for the Enhanced Detection of Drug-Induced Liver Injury.三维原代人肝细胞球体模型的评估:用于增强药物性肝损伤检测的采用和工业化。
Chem Res Toxicol. 2021 Dec 20;34(12):2485-2499. doi: 10.1021/acs.chemrestox.1c00227. Epub 2021 Nov 19.
7
Evaluation of allylated gelatin as a bioink supporting spontaneous spheroid formation of HepG2 cells.评价烯丙基化明胶作为一种生物墨水,支持 HepG2 细胞自发形成球体。
Int J Biol Macromol. 2024 Aug;274(Pt 1):133259. doi: 10.1016/j.ijbiomac.2024.133259. Epub 2024 Jun 20.
8
High-throughput confocal imaging of differentiated 3D liver-like spheroid cellular stress response reporters for identification of drug-induced liver injury liability.高通量共聚焦成像技术在分化的 3D 类肝球体细胞应激反应报告基因中的应用,用于鉴定药物诱导的肝损伤风险。
Arch Toxicol. 2019 Oct;93(10):2895-2911. doi: 10.1007/s00204-019-02552-0. Epub 2019 Aug 27.
9
A 3D cell printing-fabricated HepG2 liver spheroid model for high-content in situ quantification of drug-induced liver toxicity.一种基于 3D 细胞打印技术构建的 HepG2 肝球体模型,用于高内涵原位定量检测药物诱导的肝毒性。
Biomater Sci. 2021 Sep 7;9(17):5939-5950. doi: 10.1039/d1bm00749a. Epub 2021 Jul 27.
10
Proteomic responses of HepG2 cell monolayers and 3D spheroids to selected hepatotoxins.HepG2 细胞单层和 3D 球体对选定肝毒物的蛋白质组学反应。
Toxicol Lett. 2019 Jan;300:40-50. doi: 10.1016/j.toxlet.2018.10.030. Epub 2018 Oct 28.

引用本文的文献

1
Light-Intensity-Dependent Control of Collagen Hydrogel Properties via Riboflavin Phosphate-Mediated Photocrosslinking.通过磷酸核黄素介导的光交联对胶原水凝胶特性进行光强度依赖性控制。
Materials (Basel). 2025 Feb 14;18(4):828. doi: 10.3390/ma18040828.
2
Hydrogel-Based Strategies for Liver Tissue Engineering.基于水凝胶的肝组织工程策略
Chem Bio Eng. 2024 Sep 24;1(11):887-915. doi: 10.1021/cbe.4c00079. eCollection 2024 Dec 26.
3
Three-dimensional models: from cell culture to Patient-Derived Organoid and its application to future liposarcoma research.
三维模型:从细胞培养到患者来源的类器官及其在未来脂肪肉瘤研究中的应用。
Oncol Res. 2024 Dec 20;33(1):1-13. doi: 10.32604/or.2024.053635. eCollection 2025.
4
Spheroid-Hydrogel-Integrated Biomimetic System: A New Frontier in Advanced Three-Dimensional Cell Culture Technology.球体 - 水凝胶集成仿生系统:先进三维细胞培养技术的新前沿。
Cells Tissues Organs. 2025;214(2):128-147. doi: 10.1159/000541416. Epub 2024 Sep 12.