A beta-camera integrated with a microfluidic chip for radioassays based on real-time imaging of glycolysis in small cell populations.
A beta-camera integrated with a microfluidic chip for radioassays based on real-time imaging of glycolysis in small cell populations.
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基于小细胞群体糖酵解的实时成像,与微流体芯片集成的Beta相机。
DOI:
10.2967/jnumed.110.078725
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发表时间:
2011-05
期刊:
影响因子:
--
通讯作者:
Chatziioannou AF
中科院分区:
文献类型:
--
作者:
Vu NT;Yu ZT;Comin-Anduix B;Søndergaard JN;Silverman RW;Chang CY;Ribas A;Tseng HR;Chatziioannou AF
An integrated β-camera and microfluidic chip was developed that is capable of quantitative imaging of glycolysis radioassays using 18F-FDG in small cell populations down to a single cell. This paper demonstrates that the integrated system enables digital control and quantitative measurements of glycolysis in B-RafV600E–mutated melanoma cell lines in response to specific B-Raf inhibition. The β-camera uses a position-sensitive avalanche photodiode to detect charged particle–emitting probes within a microfluidic chip. The integrated β-camera and microfluidic chip system was calibrated, and the linearity was measured using 4 different melanoma cell lines (M257, M202, M233, and M229). Microfluidic radioassays were performed with cell populations ranging from hundreds of cells down to a single cell. The M229 cell line has a homozygous B-RafV600E mutation and is highly sensitive to a B-Raf inhibitor, PLX4032. A microfluidic radioassay was performed over the course of 3 days to assess the cytotoxicity of PLX4032 on cellular 18F-FDG uptake. The β-camera is capable of imaging radioactive uptake of 18F-FDG in microfluidic chips. 18F-FDG uptake for a single cell was measured using a radioactivity concentration of 37 MBq/mL during the radiotracer incubation period. For in vitro cytotoxicity monitoring, the β-camera showed that exposure to 1 µM PLX4032 for 3 days decreased the 18F-FDG uptake per cell in highly sensitive M229 cells, compared with vehicle controls. The integrated β-camera and microfluidic chip can provide digital control of live cell cultures and allow in vitro quantitative radioassays for multiple samples simultaneously.
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影响因子:
6.1
作者:
Lavén, M;Velikyan, I;Wallenborg, S
通讯作者:
Wallenborg, S
DOI:
10.1016/s0168-9002(01)01724-7
发表时间:
2002-02-01
影响因子:
1.4
作者:
Bertolucci, E;Conti, M;Russo, P
通讯作者:
Russo, P
影响因子:
3.5
作者:
Russo, P.;Lauria, A.;Lastoria, S.
通讯作者:
Lastoria, S.
影响因子:
56.9
作者:
Unger, MA;Chou, HP;Quake, SR
通讯作者:
Quake, SR
影响因子:
3.5
作者:
Cabello, Jorge;Bailey, Alexis;Wells, Kevin
通讯作者:
Wells, Kevin