scholarly journals Microfluidic Cell Sorter (μFCS) for On-chip Capture and Analysis of Single Cells

2012 ◽  
Vol 1 (4) ◽  
pp. 432-436 ◽  
Author(s):  
Jaehoon Chung ◽  
Huilin Shao ◽  
Thomas Reiner ◽  
David Issadore ◽  
Ralph Weissleder ◽  
...  
2012 ◽  
Vol 1 (4) ◽  
pp. 365-365
Author(s):  
Jaehoon Chung ◽  
Huilin Shao ◽  
Thomas Reiner ◽  
David Issadore ◽  
Ralph Weissleder ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Haoran Wang ◽  
Anton Enders ◽  
John-Alexander Preuss ◽  
Janina Bahnemann ◽  
Alexander Heisterkamp ◽  
...  

Abstract3D printing of microfluidic lab-on-a-chip devices enables rapid prototyping of robust and complex structures. In this work, we designed and fabricated a 3D printed lab-on-a-chip device for fiber-based dual beam optical manipulation. The final 3D printed chip offers three key features, such as (1) an optimized fiber channel design for precise alignment of optical fibers, (2) an optically clear window to visualize the trapping region, and (3) a sample channel which facilitates hydrodynamic focusing of samples. A square zig–zag structure incorporated in the sample channel increases the number of particles at the trapping site and focuses the cells and particles during experiments when operating the chip at low Reynolds number. To evaluate the performance of the device for optical manipulation, we implemented on-chip, fiber-based optical trapping of different-sized microscopic particles and performed trap stiffness measurements. In addition, optical stretching of MCF-7 cells was successfully accomplished for the purpose of studying the effects of a cytochalasin metabolite, pyrichalasin H, on cell elasticity. We observed distinct changes in the deformability of single cells treated with pyrichalasin H compared to untreated cells. These results demonstrate that 3D printed microfluidic lab-on-a-chip devices offer a cost-effective and customizable platform for applications in optical manipulation.


Author(s):  
T. Ichiki ◽  
T. Ujiie ◽  
T. Hara ◽  
Y. Horiike ◽  
K. Yasuda

2011 ◽  
Vol 79A (5) ◽  
pp. 361-367 ◽  
Author(s):  
M. Z. Islam ◽  
J. N. McMullin ◽  
Y. Y. Tsui

2017 ◽  
Vol 9 (47) ◽  
pp. 6719-6724
Author(s):  
Melinda A. Lake ◽  
Seth A. Berry ◽  
David J. Hoelzle

We demonstrate an empirical method and a balanced random forest statistical analysis to study the efficacy of microfluidic cell sorter designs with an imbalanced distribution of outcomes. The study uses polystyrene beads as model cells and studies the effects of design variables on the outcome of the beads at a Y-shaped bifurcation.


Author(s):  
Yi Gu ◽  
Rui Tang ◽  
Alex Ce Zhang ◽  
Yuanyuan Han ◽  
Yu-Hwa Lo

2014 ◽  
Vol 87 ◽  
pp. 62-65
Author(s):  
Yoshikazu Hirai ◽  
Daisuke Takagi ◽  
Satoshi Anai ◽  
Yoshitomo Chihara ◽  
Toshiyuki Tsuchiya ◽  
...  

Author(s):  
Michael Grad ◽  
Lubomir Smilenov ◽  
David Brenner ◽  
Daniel Attinger

In this work we describe the control and characterization of the switching time and hydrodynamic stress in a microfluidic cell sorter. The device was designed to sort small (<1000) populations of live cells in buffer solution labeled with standard bio-markers such as live dyes or green fluorescent protein (GFP). Sorting occurs through a hydrodynamic switching technique where high-speed solenoid valves control a sheath flow used to steer sorted cells away from the unsorted bulk population. The device is constructed from a reusable hard plastic polymethylmethacrylate (PMMA) chip machined with 127μm × 50μm microchannels and sealed with adhesive tape. Open reservoirs in the chip facilitate pipette access, standard microscope visualization, and a simple disassembly and cleaning procedure. The sorting frequency of this type of device is typically limited by the hydrodynamic switching time. Here, we present a theoretical and numerical analysis of the device switching time. These results show that the sorter switching time t is practically limited by the velocity of the flow and the characteristic length between inlet and outlet channels. We validate this theoretical result with experimental data obtained from flow visualizations, along with experiments conducted to evaluate the repeatability of the hydrodynamic switching scheme and the survival rate of sorted fibroblast cells Manually operated, the sorting frequencies were approximately 10 cells per minute, with switching time constants of approximately 130ms. Current throughput is limited by this switching time to approximately 450 cells per minute. Automation can increase the velocity and reduce the spacing between cells, thereby increasing throughput by at least an order of magnitude. The cell sorter was then tested by manually sorting 100 beads in 7 minutes, and 30 cells in less than 3 minutes, and was successfully used in the framework of a study on the bystander effect occurring during cell irradiation. Experiments with Trypan Blue dye verified that cell viability was maintained during the sorting process.


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