Osmotic erythrocyte lysis for chemical- and label-free impedance cytometry

Author(s):  
T.E. Winkler ◽  
H. Ben-Yoav ◽  
D.L. Kelly ◽  
R. Ghodssi
Lab on a Chip ◽  
2019 ◽  
Vol 19 (10) ◽  
pp. 1736-1746 ◽  
Author(s):  
Chayakorn Petchakup ◽  
Hui Min Tay ◽  
King Ho Holden Li ◽  
Han Wei Hou

A novel integrated inertial-impedance cytometer for rapid and label-free electrical profiling of neutrophil extracellular trap formation (NETosis).


Small ◽  
2021 ◽  
Vol 17 (21) ◽  
pp. 2170101
Author(s):  
Lingyan Gong ◽  
Chayakorn Petchakup ◽  
Pujiang Shi ◽  
Pei Leng Tan ◽  
Lay Poh Tan ◽  
...  

2020 ◽  
Vol 1101 ◽  
pp. 90-98 ◽  
Author(s):  
J.S. McGrath ◽  
C. Honrado ◽  
J.H. Moore ◽  
S.J. Adair ◽  
W.B. Varhue ◽  
...  

2021 ◽  
Vol 6 (1) ◽  
pp. 24
Author(s):  
Diana Isabel Sandoval Bojorquez ◽  
Eduardo Sergio Oliveros Mata ◽  
Julian Schütt ◽  
Michael Bachmann ◽  
Larysa Baraban

Impedance cytometry represents a technique that allows the electronic characterization of colloids and living cells in a highly miniaturized way. In contrast with impedance spectroscopy, the measurements are performed at a fixed frequency, providing real-time monitoring of the species traveling over the sensor. By measuring the electrical properties of particles in suspension, the dielectric characteristics (electric conductivity and capacitance) of both cells and particles can be readily determined. During the last years, this technique has been broadly investigated; however, it is still not trivial to differentiate particles of similar size based on their dielectric characteristics. A way to increase the discrimination abilities of this technique could be the integration of nanostructures into the impedance platforms. In this work, we present the impedance cytometry study of particles using microfluidic channels aligned over interdigitated gold nanowire structures as our impedimetric sensor. The characterization of particles of different sizes and their comparison with particles of different compositions will provide an understanding of the correlation between the electrical signal and the characteristics of each particle. This approach is an attractive element for label-free detection platforms that can be integrated into lab-on-a-chip systems and further implemented for single-cell analysis.


2021 ◽  
pp. 129864
Author(s):  
Chayakorn Petchakup ◽  
Paul Edward Hutchinson ◽  
Hui Min Tay ◽  
Sheng Yuan Leong ◽  
King Ho Holden Li ◽  
...  

Small ◽  
2021 ◽  
pp. 2007500
Author(s):  
Lingyan Gong ◽  
Chayakorn Petchakup ◽  
Pujiang Shi ◽  
Pei Leng Tan ◽  
Lay Poh Tan ◽  
...  

2017 ◽  
Author(s):  
King Ho Holden Li ◽  
Chayakorn Petchakup ◽  
Hui Min Tay ◽  
Nishanth Menon ◽  
Han Wei Hou

2018 ◽  
Author(s):  
Jatin Panwar ◽  
Rahul Roy

AbstractMicrofluidic impedance cytometry (MIC) provides a non-optical and label-free method for single cell detection and classification in microfluidics. However, the cleanroom intensive infrastructure required for MIC electrode fabrication limits its wide implementation in microfluidic analysis. To bypass the conventional metal (platinum) electrode fabrication protocol, we fabricated coplanar ‘in-contact’ Field’s metal (icFM) microelectrodes in multilayer elastomer devices with a single photolithography step. Our icFM microelectrodes displayed excellent and comparable performance to the platinum electrodes for detection of single erythrocytes with a lock-in amplifier based MIC setup. We further characterized it for water-in-oil droplets generated in a T-junction microfluidic channel and found high sensitivity and long-term operational stability of these electrodes. Finally, to facilitate droplet based single cell analysis, we demonstrate detection and quantification of single cells entrapped in aqueous droplets.


Author(s):  
H. J. Kirch ◽  
G. Spates ◽  
R. Droleskey ◽  
W.J. Kloft ◽  
J.R. DeLoach

Blood feeding insects have to rely on the protein content of mammalian blood to insure reproduction. A substantial quantity of protein is provided by hemoglobin present in erythrocytes. Access to hemoglobin is accomplished only via erythrocyte lysis. It has been shown that midgut homogenates from the blood feeding stable fly, Stomoxys calcitrans, contain free fatty acids and it was proposed that these detergent-like compounds play a major role as hemolysins in the digestive physiology of this species. More recently sphingomyelinase activity was detected in midgut preparations of this fly, which would provide a potential tool for the enzymatic cleavage of the erythrocyte's membrane sphingomyelin. The action of specific hemolytic factors should affect the erythrocyte's morphology. The shape of bovine erythrocytes undergoing in vitro hemolysis by crude midgut homogenates from the stable fly was examined by scanning and transmission electron microscopy.


2020 ◽  
Author(s):  
Nikolas Hundt

Abstract Single-molecule imaging has mostly been restricted to the use of fluorescence labelling as a contrast mechanism due to its superior ability to visualise molecules of interest on top of an overwhelming background of other molecules. Recently, interferometric scattering (iSCAT) microscopy has demonstrated the detection and imaging of single biomolecules based on light scattering without the need for fluorescent labels. Significant improvements in measurement sensitivity combined with a dependence of scattering signal on object size have led to the development of mass photometry, a technique that measures the mass of individual molecules and thereby determines mass distributions of biomolecule samples in solution. The experimental simplicity of mass photometry makes it a powerful tool to analyse biomolecular equilibria quantitatively with low sample consumption within minutes. When used for label-free imaging of reconstituted or cellular systems, the strict size-dependence of the iSCAT signal enables quantitative measurements of processes at size scales reaching from single-molecule observations during complex assembly up to mesoscopic dynamics of cellular components and extracellular protrusions. In this review, I would like to introduce the principles of this emerging imaging technology and discuss examples that show how mass-sensitive iSCAT can be used as a strong complement to other routine techniques in biochemistry.


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