脐静脉
基质凝胶
血管内皮生长因子
原位
基质(化学分析)
癌细胞
材料科学
细胞外基质
化学
生物医学工程
微流控
纳米技术
细胞培养
生物物理学
细胞生物学
细胞
癌症研究
癌症
体外
血管内皮生长因子受体
生物
生物化学
医学
有机化学
遗传学
复合材料
作者
Ziting Qian,Jiayuan Fei,Shenfei Zong,Kuo Yang,Lang Li,Ruiyang Liu,Zhuyuan Wang,Yiping Cui
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2019-12-30
卷期号:5 (1): 208-216
被引量:27
标识
DOI:10.1021/acssensors.9b02085
摘要
A multifunctional microfluidic platform was demonstrated to monitor the interaction between tumor cells and endothelial cells by integrating a three-dimensional (3D) cell culture unit with a protein detection unit. In such a chip, breast cancer cells MCF7 were seeded into the collagen to form a 3D tumor environment while human umbilical vein endothelial cells (HUVECs) are seeded in the channel next to the collagen matrix. Thus, an in situ growth of angiogenic sprouting can be visualized through fluorescence in the 3D collagen matrix after a coculture of MCF7 and HUVEC after 4 days, which cannot be observed in the 2D culture environment. On the other hand, gold@silver core-shell nanorods were used as surface-enhanced Raman scattering (SERS) immunoprobes for the detection of the secretion of cytokine (vascular endothelial growth factor, VEGF). The limit of detection of the VEGF is 100 pg/mL. Further, as LiCl and bevacizumab can act as a promoter and an inhibitor of VEGF, the dynamic change of the concentration of VEGF under the stimulation of them was monitored by SERS signals. Thus, this integrated SERS microfluidic platform creates opportunity for the fundamental research of interaction between tumors and endothelial cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI