scholarly journals Sorting droplets into many outlets

Lab on a Chip ◽  
2021 ◽  
Author(s):  
Saurabh Vyawahare ◽  
Michael Brundage ◽  
Aleksandra Kijac ◽  
Michael Gutierrez ◽  
Martina de Geus ◽  
...  

Droplet sorter manufacturable in plastic (COC) or elastomer (PDMS), featuring ionic liquid electrodes and stackable sorting junctions. We use it to make a cell sorter, introducing methods for breaking emulsions and collecting single droplets.

2019 ◽  
Vol 33 ◽  
pp. 100574 ◽  
Author(s):  
Ngoc Tan Nguyen ◽  
Mirza Saquib Sarwar ◽  
Claire Preston ◽  
Aziliz Le Goff ◽  
Cédric Plesse ◽  
...  

1979 ◽  
Vol 27 (1) ◽  
pp. 280-283 ◽  
Author(s):  
J T Merrill ◽  
P N Dean ◽  
J W Gray

We have investigated the accuracy with which droplets containing cells can be sorted individually onto known and thus relocatable positions. The presence and random arrival of cells and particles in the sorter jet disturbs the orderly production and deflection of droplets, causing a dispersion of sorted droplet trajectories. The magnitude of this dispersion is a function of the phase relationship between the arrival of a cell at the end of the jet and the droplet formation. Using a modified Becton Dickinson Fluorescence-Activated Cell Sorter, we selected for sorting only those droplets that formed with a cell near the center of the droplet. We used this technique to sort Lewis lung tumor cells. The dispersion of droplet positions was reduced from over 3% to about 1% of an average deflection of typically 15 mm for a nozzle with a 50-micron diameter orifice. Sorting onto a surface such as magnetic tape or a microscope slide introduces another uncertainty in position because the cell may be located anywhere within the wetted radius of the droplet on the slide. Sorting onto less-wettable surfaces reduces the wetted radius and thus the variation in cell position.


2021 ◽  
Author(s):  
Agnes Heering ◽  
Ivo Leito ◽  
Markus Lahe ◽  
Martin Vilbaste

The purpose of this document is to present technical guidance of measuring pHabsH2O difference (ΔpHabsH2O value) between two solutions by differential potentiometry in a cell with two compartments connected by a salt bridge filled with an ionic liquid.


Biomaterials ◽  
2010 ◽  
Vol 31 (32) ◽  
pp. 8445-8453 ◽  
Author(s):  
Chien-Chen Lin ◽  
Mei-Hui Ni ◽  
Yu-Chung Chang ◽  
Hsiu-Lun Yeh ◽  
Feng-Huei Lin

2013 ◽  
Vol 21 (6) ◽  
pp. 472-484 ◽  
Author(s):  
Afsaneh Safavi ◽  
Norooz Maleki ◽  
Farzaneh Aghakhani Mahyari ◽  
Mohammad Mahdi Doroodmand

Blood ◽  
1980 ◽  
Vol 56 (5) ◽  
pp. 923-925 ◽  
Author(s):  
ME Osband ◽  
EB Cohen ◽  
RP McCaffrey ◽  
HM Shapiro

Abstract Histamine receptors have been demonstrated on lymphocyte membranes by a variety of techniques. We now report a method that allows for the flow cytometric analysis of histamine receptors on human peripheral T cells. Histamine is conjugated to fluoresceinated human albumin by the coupling agent ECDI. This conjugated histamine compound (FHA-his) binds to approximately 45% of T cells. Fluoresceinated human albumin alone (FHA), not conjugated to histamine, does not bind to T cells. In addition, unconjugated histamine can inhibit completely the binding seen with FHA-his. We conclude that this technique demonstrates specific FHA-his binding to histamine receptors on T cells and can be used to determine the number of cells bearing such receptors. In addition, the reagent could be used with a cell sorter to isolate distinct histamine-receptor-bearing (HR+) cells for further immunologic study.


2016 ◽  
Vol 01 (01) ◽  

Objective: When cells are incubated with various particles in phagocytosis experiment, the cells include two populations. One is the population which engulfed the particles; the other is the population which did not engulf them. We separated both populations by use of a cell sorter and evaluated the cell death of the population which engulfed the particles to clarify the cytotoxic effect by the phagocytized particles in this study. Methods and Results: Thioglycollate-elicited peritoneal macrophages engulfed 100 nm and 1000 nm of non-crystalline silica and polystyrene particles. Phagocytosis of these particles increased depending on the quantity of added particles. The treatment of the cells with 1000 nm silica particles induced release of lactate dehydrogenase (LDH) and production of interleukin-1β (IL-1β). On the other hand, 100 nm silica particles did not increase the LDH release and the IL-1β production. Polystyrene particles also did not have cytotoxic and inflammatory effects. To elucidate the relation of phagocytosis and cytotoxicity, the cells incubated with 1000 nm silica particles were divided into non-phagocytic and phagocytic population by use of a cell sorter. As most of dead cells stained by propidium iodide were observed in the phagocytic cells population, the phagocytosis of 1000 nm silica particle was associated with cell damage directly. The silica-induced cell death was not accompanied with the externalization of phosphatidylserine in the plasma membrane. Conclusions: These results indicated the following things: (1) The engulfment of certain size of the silica particles induced cell death in the macrophages, (2) The cell death was not typical apoptosis and (3) The cell death was accompanied with the activation of inflammasome.


Development ◽  
1985 ◽  
Vol 88 (1) ◽  
pp. 15-24
Author(s):  
Marianne Krefft ◽  
Ludwig Voet ◽  
James H. Gregg ◽  
Keith L. Williams

Double labelling experiments on Dictyostelium discoideum cells at different developmental stages were carried out using monoclonal antibodies MUD1 (prespore specific), MUD9 (strong label on prestalk and anterior-like cells) and a fluorescence-activated cell sorter. The monoclonal antibody MUD9, which recognizes the surface of prestalk and anterior-like cells strongly and prespore cells weakly, is also present on the surface of vegetative amoebae and on mature stalk cells but not on the spore surface. Sharing of an antigenic determinant between vegetative, prestalk and anterior-like cells is consistent with these cells being ‘less differentiated’ than prespore cells.


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