Continuous inertial focusing, ordering, and separation of particles in microchannels
By D. Di Carlo, D. Irimia, R. Tompkins, Mehmet Toner. Proceedings of the National Academy of Sciences of the United States of America, 2007
1,696 citations recorded by the source corpus.
Subfields: Biomedical Engineering, Electrical and Electronic Engineering
View Paper: https://www.semanticscholar.org/paper/2da397a79a8916b2de055a60cb36781e13a239f9
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomedical Engineering
- Nam-Trung Nguyen
- Jeffrey F. Morris
- Jean-Philippe Matas
- É. Guazzelli
- D. Di Carlo
- Xiangchun Xuan
- Junjie Zhu
- Christopher Church
In Electrical and Electronic Engineering
- Nam-Trung Nguyen
- Xiangchun Xuan
- Junjie Zhu
- Christopher Church
- Mehmet Toner
- Weihua Li
- Jeffrey F. Morris
- Jongyoon Han
Citations in the corpus
- Particle focusing in microfluidic devices (2010, methodology): “Reprinted from Di Carlo et al. (2007) with permission from PNAS, National Academy of Sciences Fig. 10 Inertial focusing of 7 lm polymer beads in a straight multiorifice microchannel at different particle Reynolds numbers, Rep.”
- Label-free cell separation and sorting in microfluidic systems (2010, background): “Lastly, their independence from external force fields eases their integration into massively parallel systems [65, 73].”
- Particle inertial focusing and its mechanism in a serpentine microchannel (2014, background): “Di Carlo et al. (2007) introduced an asymmetric serpentine channel to focus particles into one streak in 2D (top view), and later, this asymmetric serpentine channel was combined with a straight section to successfully focus particles in 3D.”
- Inertial Focusing for Tumor Antigen–Dependent and –Independent Sorting of Rare Circulating Tumor Cells (2013, methodology): “After the magnetic labeling of cells in whole blood, this capture platform integrates three sequential microfluidic technologies within a single automated system: (i) debulking by separation of nucleated cells, including CTCs and white blood cells (WBCs), from red blood cells (RBCs) and platelets us”