肺癌
阿法替尼
吉非替尼
肺
癌症研究
医学
埃罗替尼
药理学
癌症
病理
表皮生长因子受体
内科学
作者
Jianfeng Tan,Xindi Sun,Jianhua Zhang,Huili Li,Jun Kuang,Lulu Xu,Xinghua Gao,Chengbin Zhou
出处
期刊:Biosensors
[Multidisciplinary Digital Publishing Institute]
日期:2022-08-09
卷期号:12 (8): 618-618
被引量:21
摘要
In this study, we used three-dimensional (3D) printing to prepare a template of a microfluidic chip from which a polydimethylsiloxane (PDMS)lung chip was successfully constructed. The upper and lower channels of the chip are separated by a microporous membrane. The upper channel is seeded with lung cancer cells, and the lower channel is seeded with vascular endothelial cells and continuously perfused with cell culture medium. This lung chip can simulate the microenvironment of lung tissue and realize the coculture of two kinds of cells at different levels. We used a two-dimensional (2D) well plate and a 3D lung chip to evaluate the effects of different EGFR-targeting drugs (gefitinib, afatinib, and osimertinib) on tumor cells. The 3D lung chip was superior to the 2D well plate at evaluating the effect of drugs on the NCI-H650, and the results were more consistent with existing clinical data. For primary tumor cells, 3D lung chips have more advantages because they simulate conditions that are more similar to the physiological cell microenvironment. The evaluation of EGFR-targeted drugs on lung chips is of great significance for personalized diagnosis and treatment and pharmacodynamic evaluation.
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