Optofluidic chip for single cell trapping and stretching fabricated by a femtosecond laser

2010 ◽  
Vol 3 (4) ◽  
pp. 234-243 ◽  
Author(s):  
Francesca Bragheri ◽  
Lorenzo Ferrara ◽  
Nicola Bellini ◽  
Krishna C. Vishnubhatla ◽  
Paolo Minzioni ◽  
...  
Author(s):  
L. Ferrara ◽  
F. Bragheri ◽  
P. Minzioni ◽  
I. Cristiani ◽  
K. C. Vishnubhatla ◽  
...  

Author(s):  
Francesca Bragheri ◽  
Roberto Osellame

AbstractSingle cell sorting based either on fluorescence or on mechanical properties has been exploited in the last years in microfluidic devices. Hydrodynamic focusing allows increasing the efficiency of theses devices by improving the matching between the region of optical analysis and that of cell flow. Here we present a very simple solution fabricated by femtosecond laser micromachining that exploits flow laminarity in microfluidic channels to easily lift the sample flowing position to the channel portion illuminated by the optical waveguides used for single cell trapping and analysis.


Lab on a Chip ◽  
2021 ◽  
Author(s):  
Huichao Chai ◽  
Yongxiang Feng ◽  
Fei Liang ◽  
Wenhui Wang

Successful single-cell isolation is a pivotal technique for subsequent biological and chemical analysis of single cells. Although significant advances have been made in single-cell isolation and analysis techniques, most passive...


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
B. Deng ◽  
X. F. Li ◽  
D. Y. Chen ◽  
L. D. You ◽  
J. B. Wang ◽  
...  

Microfluidic cell-based arraying technology is widely used in the field of single-cell analysis. However, among developed devices, there is a compromise between cellular loading efficiencies and trapped cell densities, which deserves further analysis and optimization. To address this issue, the cell trapping efficiency of a microfluidic device with two parallel micro channels interconnected with cellular trapping sites was studied in this paper. By regulating channel inlet and outlet status, the microfluidic trapping structure can mimic key functioning units of previously reported devices. Numerical simulations were used to model this cellular trapping structure, quantifying the effects of channel on/off status and trapping structure geometries on the cellular trapping efficiency. Furthermore, the microfluidic device was fabricated based on conventional microfabrication and the cellular trapping efficiency was quantified in experiments. Experimental results showed that, besides geometry parameters, cellular travelling velocities and sizes also affected the single-cell trapping efficiency. By fine tuning parameters, more than 95% of trapping sites were taken by individual cells. This study may lay foundation in further studies of single-cell positioning in microfluidics and push forward the study of single-cell analysis.


2009 ◽  
Vol 24 (12) ◽  
pp. 3637-3644 ◽  
Author(s):  
Ling-Sheng Jang ◽  
Pao-Hua Huang ◽  
Kung-Chieh Lan

2016 ◽  
Vol 32 (3) ◽  
pp. 422-429 ◽  
Author(s):  
Miao Yu ◽  
Zongzheng Chen ◽  
Cheng Xiang ◽  
Bo Liu ◽  
Handi Xie ◽  
...  

Lab on a Chip ◽  
2010 ◽  
Vol 10 (7) ◽  
pp. 857 ◽  
Author(s):  
Stefan Kobel ◽  
Ana Valero ◽  
Jonas Latt ◽  
Philippe Renaud ◽  
Matthias Lutolf

Lab on a Chip ◽  
2017 ◽  
Vol 17 (23) ◽  
pp. 4077-4088 ◽  
Author(s):  
Lindong Weng ◽  
Felix Ellett ◽  
Jon Edd ◽  
Keith H. K. Wong ◽  
Korkut Uygun ◽  
...  

A passive pumping, single-cell trapping microarray was developed to monitor volumetric change of multiple, single cells following hypertonic exposure.


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