Selective digestion of Ba2+/Ca2+ alginate gel microdroplets for single-cell handling

2018 ◽  
Vol 57 (6S1) ◽  
pp. 06HH02
Author(s):  
Masao Odaka ◽  
Akihiro Hattori ◽  
Kenji Matsuura ◽  
Kenji Yasuda
Lab on a Chip ◽  
2019 ◽  
Vol 19 (24) ◽  
pp. 4016-4020 ◽  
Author(s):  
Neus Godino ◽  
Felix Pfisterer ◽  
Tobias Gerling ◽  
Christian Guernth-Marschner ◽  
Claus Duschl ◽  
...  

We employ real-time image processing in the active control of dielectrophoretic actuation to select, isolate and arrange individual cells in a microfluidic channel.


2020 ◽  
Vol 20 (07) ◽  
pp. 2050050
Author(s):  
ROOZBEH ABEDINI-NASSAB

Recently, we introduced magnetophoretic circuits, composed of overlaid magnetic and metallic layers, as a novel single-cell analysis (SCA) tool. We showed the ability of these circuits in organizing large single-particle and particle-pair arrays. Assembling the cells in microarrays is performed with the ultimate goal of running temporal phenotypic analyses. However, for long-term studies, a suitable microenvironment for the cells to normally grow and differentiate is needed. Towards this goal, in this study, we run required biocompatibility tests, based on which we make the magnetophoretic-based microchip a suitable home for the cells to grow. The results confirm the ability of these chips in cell handling and show no unwanted cell behavior alteration due to the applied shear stress on them, the magnetic labeling, or the microenvironment. After this achievement, this tool would be ready for running important single-cell studies in oncology, virology, and medicine.


Lab on a Chip ◽  
2017 ◽  
Vol 17 (5) ◽  
pp. 855-863 ◽  
Author(s):  
John J. Kim ◽  
Elly Sinkala ◽  
Amy E. Herr

We demonstrate a lab-on-a-disc western blotting device that integrates cell handling and single-cell protein analysis of sparse (<200 cells) starting samples.


Author(s):  
Debby A. Jennings ◽  
Michael J. Morykwas ◽  
Louis C. Argenta

Grafts of cultured allogenic or autogenic keratlnocytes have proven to be an effective treatment of chronic wounds and burns. This study utilized a collagen substrate for keratinocyte and fibroblast attachment. The substrate provided mechanical stability and augmented graft manipulation onto the wound bed. Graft integrity was confirmed by light and transmission electron microscopy.Bovine Type I dermal collagen sheets (100 μm thick) were crosslinked with 254 nm UV light (13.5 Joules/cm2) to improve mechanical properties and reduce degradation. A single cell suspension of third passage neonatal foreskin fibroblasts were plated onto the collagen. Five days later, a single cell suspension of first passage neonatal foreskin keratinocytes were plated on the opposite side of the collagen. The grafts were cultured for one month.The grafts were fixed in phosphate buffered 4% formaldehyde/1% glutaraldehyde for 24 hours. Graft pieces were then washed in 0.13 M phosphate buffer, post-fixed in 1% osmium tetroxide, dehydrated, and embedded in Polybed 812.


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