Organ-on-a-chip for dynamic tumor drug resistance investigation

被引:19
作者
Shao, Changmin [1 ,2 ]
Yu, Yunru [1 ,3 ]
Lei, Xin [1 ]
Cao, Jie [1 ]
Zhao, Yuanjin [1 ,3 ]
Ye, Fangfu [1 ,2 ,4 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Joint Ctr Translat Med, Wenzhou 325035, Peoples R China
[2] Univ Chinese Acad Sci, Wenzhou Inst, Zhejiang Engn Res Ctr Tissue Repair Mat, Joint Ctr Translat Med, Wenzhou 325000, Peoples R China
[3] Southeast Univ, Nanjing Drum Tower Hosp, Sch Biol Sci & Med Engn, Dept Clin Lab, Nanjing 210096, Peoples R China
[4] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Microfluidics; Cell spheroid; Organ-on-a-chip; Inverse opal; Drug resistance; CANCER; CULTURE;
D O I
10.1016/j.cej.2023.141739
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
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.
引用
收藏
页数:7
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