A microchip integrating cell array positioning with in situ single-cell impedance measurement

The Analyst ◽  
2015 ◽  
Vol 140 (19) ◽  
pp. 6571-6578 ◽  
Author(s):  
Xiaoliang Guo ◽  
Rong Zhu ◽  
Xianli Zong

A micro-chip integrating cell positioning with in situ, real-time and long-time impedance measurement on a single cell using nano-modified measuring electrodes.

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Hervé Straub ◽  
Leo Eberl ◽  
Manfred Zinn ◽  
René M. Rossi ◽  
Katharina Maniura-Weber ◽  
...  

Abstract Background Studying bacterial adhesion and early biofilm development is crucial for understanding the physiology of sessile bacteria and forms the basis for the development of novel antimicrobial biomaterials. Microfluidics technologies can be applied in such studies since they permit dynamic real-time analysis and a more precise control of relevant parameters compared to traditional static and flow chamber assays. In this work, we aimed to establish a microfluidic platform that permits real-time observation of bacterial adhesion and biofilm formation under precisely controlled homogeneous laminar flow conditions. Results Using Escherichia coli as the model bacterial strain, a microfluidic platform was developed to overcome several limitations of conventional microfluidics such as the lack of spatial control over bacterial colonization and allow label-free observation of bacterial proliferation at single-cell resolution. This platform was applied to demonstrate the influence of culture media on bacterial colonization and the consequent eradication of sessile bacteria by antibiotic. As expected, the nutrient-poor medium (modified M9 minimal medium) was found to promote bacterial adhesion and to enable a higher adhesion rate compared to the nutrient-rich medium (tryptic soy broth rich medium ). However, in rich medium the adhered cells colonized the glass surface faster than those in poor medium under otherwise identical conditions. For the first time, this effect was demonstrated to be caused by a higher retention of newly generated bacteria in the rich medium, rather than faster growth especially during the initial adhesion phase. These results also indicate that higher adhesion rate does not necessarily lead to faster biofilm formation. Antibiotic treatment of sessile bacteria with colistin was further monitored by fluorescence microscopy at single-cell resolution, allowing in situ analysis of killing efficacy of antimicrobials. Conclusion The platform established here represents a powerful and versatile tool for studying environmental effects such as medium composition on bacterial adhesion and biofilm formation. Our microfluidic setup shows great potential for the in vitro assessment of new antimicrobials and antifouling agents under flow conditions.


The Analyst ◽  
2012 ◽  
Vol 137 (13) ◽  
pp. 3011 ◽  
Author(s):  
Fareid Asphahani ◽  
Myo Thein ◽  
Kui Wang ◽  
David Wood ◽  
Sau Shun Wong ◽  
...  

Author(s):  
Justin Gullotta ◽  
Lakshmi Krishnan ◽  
Dylan Share ◽  
Daniel Walczyk ◽  
Raymond Puffer

The most critical step in high temperature proton exchange membrane (PEM) MEA manufacturing is sealing of the membrane between the two electrodes. This sealing process is typically conducted using a precision hydraulic thermal press. In order to achieve cost-effective high-volume MEA manufacturing, it is important to reduce the variability in MEA performance due to variations in incoming material properties and dimensions, and to reduce the unit process cycle time. This paper explains the application of real time adaptive process controls (APC) combined with effective in-situ diagnostics during the MEA sealing process to achieve greater uniformity and performance of high temperature PEM MEAs. The in-situ impedance measurement is carried out in a precision thermal press using a milliohmmeter by reading the complex impedance of the MEA at 1 kHz as the components of the MEA are sealed. This signal is then used to adjust the pressing process parameters in real time to achieve more uniform MEA performance. An experiment was carried out in an attempt to identify the impedance parameter which correlated most closely with the MEA’s future performance. Using these impedance parameters during pressing, we are able to reliably produce MEAs using the real time APC technique that perform consistently in a single cell test fixture with more than a 50% reduction in pressing time.


Author(s):  
Anna Maria Marbà-Ardébol ◽  
Joern Emmerich ◽  
Michael Muthig ◽  
Peter Neubauer ◽  
Stefan Junne

Lab on a Chip ◽  
2013 ◽  
Vol 13 (7) ◽  
pp. 1316 ◽  
Author(s):  
Yingru Liu ◽  
Brett Kirkland ◽  
James Shirley ◽  
Zhibin Wang ◽  
Peipei Zhang ◽  
...  

Author(s):  
Lin Zhou ◽  
Nahoko Kasai ◽  
Hizuru Nakajima ◽  
Shungo Kato ◽  
Sifeng Mao ◽  
...  

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