脚手架
微流控芯片
抗药性
药品
同种类的
炸薯条
球体
生物医学工程
计算机科学
癌症研究
纳米技术
材料科学
药理学
化学
医学
生物
体外
微流控
电信
生物化学
物理
微生物学
热力学
作者
Changmin Shao,Yunru Yu,Lei Xin,Jie Cao,Yuanjin Zhao,Fangfu Ye
标识
DOI:10.1016/j.cej.2023.141739
摘要
Drug resistance continues to be the main limiting factor in the cure of cancer patients. Herein, an organ-on-a-chip platform based on inverse opal scaffold was proposed to generate tumor cell spheroids and study resistance dynamically. The relevant inverse opal scaffold with desired tridimensional porous structure was prepared by negatively replicating the assembled microfluidic droplet template. Benefitting from the ordered and uniform porous structure of the inverse opal scaffolds, hepatoma cells could aggregate in the pores of the scaffold and form large amounts of homogeneous hepatoma cell spheroids. The proposed liver tumor-on-a-chip was established by integrating the inverse opal scaffolds with a well-designed gradient microfluidic chip. The liver tumor models with varying degrees of drug-resistant phenotypes were realized by simply gradient injection of hepatoma parental and resistant cells into the microfluidic chip. Based on the resultant system, we have obtained the dynamic drug resistance performance of different tumor stages and diverse medication periods, which will provide extremely significant preclinical data for drug therapy of tumors. These features make the proposed organ-on-a-chip platform a valuable candidate for preclinical drug resistance evaluation.
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