scholarly journals Fluorescence-Activated on-Chip Cell Culture Sorting (O3CS): Smart Petri Dish

Author(s):  
Molchanov Pavel G ◽  
Moreno-Cuevas Jorge E ◽  
Hernández Martin ◽  
Gonzalez-Garza Maria Teresa ◽  
Garcia Charles ◽  
...  
Keyword(s):  
Lab on a Chip ◽  
2013 ◽  
Vol 13 (18) ◽  
pp. 3714 ◽  
Author(s):  
Bi-Yi Xu ◽  
Shan-Wen Hu ◽  
Guang-Sheng Qian ◽  
Jing-Juan Xu ◽  
Hong-Yuan Chen

Author(s):  
Guoan Zheng ◽  
Seung Ah Lee ◽  
Xiaoze Ou ◽  
Changhuei Yang
Keyword(s):  

2018 ◽  
Vol 115 (26) ◽  
pp. E5926-E5933 ◽  
Author(s):  
Cristian Soitu ◽  
Alexander Feuerborn ◽  
Ann Na Tan ◽  
Henry Walker ◽  
Pat A. Walsh ◽  
...  

Many proofs of concept have demonstrated the potential of microfluidics in cell biology. However, the technology remains inaccessible to many biologists, as it often requires complex manufacturing facilities (such as soft lithography) and uses materials foreign to cell biology (such as polydimethylsiloxane). Here, we present a method for creating microfluidic environments by simply reshaping fluids on a substrate. For applications in cell biology, we use cell media on a virgin Petri dish overlaid with an immiscible fluorocarbon. A hydrophobic/fluorophilic stylus then reshapes the media into any pattern by creating liquid walls of fluorocarbon. Microfluidic arrangements suitable for cell culture are made in minutes using materials familiar to biologists. The versatility of the method is demonstrated by creating analogs of a common platform in cell biology, the microtiter plate. Using this vehicle, we demonstrate many manipulations required for cell culture and downstream analysis, including feeding, replating, cloning, cryopreservation, lysis plus RT-PCR, transfection plus genome editing, and fixation plus immunolabeling (when fluid walls are reconfigured during use). We also show that mammalian cells grow and respond to stimuli normally, and worm eggs develop into adults. This simple approach provides biologists with an entrée into microfluidics.


Micromachines ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 369 ◽  
Author(s):  
Yu-suke Torisawa ◽  
Yi-Chung Tung

Recent advances in microsystems technology and cell culture techniques have led to the development of organ-on-chip microdevices to model functional units of organs [...]


IEEE Access ◽  
2020 ◽  
Vol 8 ◽  
pp. 70733-70745
Author(s):  
Yumin Liao ◽  
Ningmei Yu ◽  
Dian Tian ◽  
Chen Wang ◽  
Shuaijun Li ◽  
...  

2019 ◽  
Vol 9 (4) ◽  
pp. 621 ◽  
Author(s):  
Samira Uharek ◽  
Sara Baratchi ◽  
Jiu Zhu ◽  
Majed Alshehri ◽  
Arnan Mitchell ◽  
...  

Water jacket systems are routinely used to control the temperature of Petri dish cell culture chambers. Despite their widespread use, the thermal characteristics of such systems have not been fully investigated. In this study, we conducted a comprehensive set of theoretical, numerical and experimental analyses to investigate the thermal characteristics of Petri dish chambers under stable and transient conditions. In particular, we investigated the temperature gradient along the radial axis of the Petri dish under stable conditions, and the transition period under transient conditions. Our studies indicate a radial temperature gradient of 3.3 °C along with a transition period of 27.5 min when increasing the sample temperature from 37 to 45 °C for a standard 35 mm diameter Petri dish. We characterized the temperature gradient and transition period under various operational, geometric, and environmental conditions. Under stable conditions, reducing the diameter of the Petri dish and incorporating a heater underneath the Petri dish can effectively reduce the temperature gradient across the sample. In comparison, under transient conditions, reducing the diameter of the Petri dish, reducing sample volume, and using glass Petri dish chambers can reduce the transition period.


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