294:. Not only does this allow for the ease of manipulating the environment of the cells, but having an open channel wall allows for a better understanding of biological interactions at this interface. Creating designs of microfluidic platforms with different compartments that are isolated and have different dimensions allows for co-culturing of several types of cells. These devices often incorporate droplet formation to encapsulate cells and act as transport and reaction vehicles in two or more immiscible phases, making it possible to carry out numerous parallel analyses using different conditions. Open microfluidics has also been coupled with fluorescence-activated
269:(SCF), and exposes cells to the surrounding environment. The miniaturization of this process allows for improved sensitivity, high throughput, and ease of manipulation and integration, as well as dimensions that can be more physiologically relevant. The benefits of both open and closed microfluidic platforms have allowed the option for the combination of the two, where the device is open for the introduction and culturing of cells, and can be sealed prior to analysis.
63:
22:
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298:(FACS) to allow for cells to be contained in individually sorted compartments in an open microfluidic network for culturing in an exposed environment. The exposure of one of the channel walls introduces the issue of evaporation and therefore cell loss, however this issue can be minimized by using droplet microfluidics where the cell-containing droplets are submerged in a
289:
conditioned medium to simulate the desired cell populations in traditional close-channel microfluidic devices. The challenge to support the cell growth and simultaneously study multiple cell types in a single device with an exposed channel is that the interactions between cells in this medium needs
326:
into the culture medium have both been posed as issues of using PDMS for biological studies, however these can be reduced by adopting pretreatment procedures to create optimal environments. Advantages of using PDMS include the ease of surface modification, low cost, biocompatibility, and optical
358:
and the cell culture medium is passively transported to the culture areas. A major advantage of this type of open-microfluidics includes the low cost, the variety of dimensions of porous papers that are commercially available, improved cell viability, adhesion, and migration over tissue culture
302:
oil. Although evaporation is a major disadvantage of using an open microfluidic system for cell culturing, the advantages over a closed system include ease of manipulation and access to the cells. For certain applications, such as the study of drug transport and lung function using
343:. Devices created with polystyrene by these methods include microfluidic platforms that integrate several microfluidic systems, creating arrays to study several cell cultures simultaneously. Another type of material that is used for open-microfluidic cell culturing is
327:
transparency. In addition, PDMS is an attractive material to use for generating oxygen gradients for cell culturing in studies that involve monitoring ROS governed cellular pathways due to its oxygen permeability. Plastics such as
688:
Nalayanda, Divya D.; Puleo, Christopher; Fulton, William B.; Sharpe, Leilani M.; Wang, Tza-Huei; Abdullah, Fizan (2009-05-30). "An open-access microfluidic model for lung-specific functional studies at an air-liquid interface".
387:
Lin, Dongguo; Li, Peiwen; Lin, Jinqiong; Shu, Bowen; Wang, Weixin; Zhang, Qiong; Yang, Na; Liu, Dayu; Xu, Banglao (2017-10-31). "Orthogonal
Screening of Anticancer Drugs Using an Open-Access Microfluidic Tissue Array System".
1300:
YAN, Wei; ZHANG, Qiong; CHEN, Bin; LIANG, Guang-Tie; LI, Wei-Xuan; ZHOU, Xiao-Mian; LIU, Da-Yu (June 2013). "Study on
Microenvironment Acidification by Microfluidic Chip with Multilayer-paper Supported Breast Cancer Tissue".
359:
plates. In addition, it is an attractive substrate for 3D cell culture devices due to its ability to incorporate essential characteristics such as oxygen and nutrient gradients, fluid flow that can control
290:
to be controlled since the timing and location of the interactions is critical. This issue can be addressed in several ways including the modification of the device design, using droplet microfluidics, and
967:
Regehr, Keil J.; Domenech, Maribella; Koepsel, Justin T.; Carver, Kristopher C.; Ellison-Zelski, Stephanie J.; Murphy, William L.; Schuler, Linda A.; Alarid, Elaine T.; Beebe, David J. (2009).
491:
Lovchik, Robert D.; Bianco, Fabio; Tonna, Noemi; Ruiz, Ana; Matteoli, Michela; Delamarche, Emmanuel (May 2010). "Overflow
Microfluidic Networks for Open and Closed Cell Cultures on Chip".
281:
can be patterned in microfluidic devices with one of the channel walls exposed in different geometries and designs depending on the behaviors and interactions to be studied, such as
829:
Birchler, Axel; Berger, Mischa; Jäggin, Verena; Lopes, Telma; Etzrodt, Martin; Misun, Patrick Mark; Pena-Francesch, Maria; Schroeder, Timm; Hierlemann, Andreas (2016-01-06).
1023:
Halldorsson, S., Lucumi, E., Gómez-Sjöberg, R., & Fleming, R. M. T. (2015). Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices.
831:"Seamless Combination of Fluorescence-Activated Cell Sorting and Hanging-Drop Networks for Individual Handling and Culturing of Stem Cells and Microtissue Spheroids"
1075:
Young, Edmond W. K.; Berthier, Erwin; Guckenberger, David J.; Sackmann, Eric; Lamers, Casey; Meyvantsson, Ivar; Huttenlocher, Anna; Beebe, David J. (2011-02-15).
742:"Microfluidic Confinement of Single Cells of Bacteria in Small Volumes Initiates High-Density Behavior of Quorum Sensing and Growth and Reveals Its Variability"
186:
35:
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Kaigala, G. V., Lovchik, R. D., & Delamarche, E. (2012). Microfluidics in the “open Space” for performing localized chemistry on biological interfaces.
84:
77:
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Ng, K., Gao, B., Yong, K. W., Li, Y., Shi, M., Zhao, X., … Xu, F. (2017). Paper-based cell culture platform and its emerging biomedical applications.
639:
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Casavant, B. P., Berthier, E., Theberge, A. B., Berthier, J., Montanez-Sauri, S. I., Bischel, L. L., … Beebe, D. J. (2013). Suspended microfluidics.
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Lee, J. J., Berthier, J., Brakke, K. A., Dostie, A. M., Theberge, A. B., & Berthier, E. (2018). Droplet
Behavior in Open Biphasic Microfluidics.
127:
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Mosadegh, Bobak; Dabiri, Borna E.; Lockett, Matthew R.; Derda, Ratmir; Campbell, Patrick; Parker, Kevin Kit; Whitesides, George M. (2014-02-12).
99:
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Lee, Sung Hoon; Heinz, Austen James; Shin, Sunghwan; Jung, Yong-Gyun; Choi, Sung-Eun; Park, Wook; Roe, Jung-Hye; Kwon, Sunghoon (April 2010).
433:"An open access microfluidic device for the study of the physical limits of cancer cell deformation during migration in confined environments"
106:
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113:
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Lo, J. F., Sinkala, E., & Eddington, D. T. (2010). Oxygen gradients for open well cellular cultures via microfluidic substrates.
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Li, Chao; Yu, Jiaquan; Schehr, Jennifer; Berry, Scott M.; Leal, Ticiana A.; Lang, Joshua M.; Beebe, David J. (2018-05-08).
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or co-culturing of several types of cells. A majority of cell culturing has been carried out by introducing the cells in a
318:(PDMS) is a common material for open microfluidic devices that introduces additional advantages and disadvantages. The
912:"Exclusive Liquid Repellency: An Open Multi-Liquid-Phase Technology for Rare Cell Culture and Single-Cell Processing"
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Guckenberger, David J.; de Groot, Theodorus E.; Wan, Alwin M. D.; Beebe, David J.; Young, Edmond W. K. (2015).
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Tao, F. F., Xiao, X., Lei, K. F., & Lee, I. C. (2015). Paper-based cell culture microfluidic system.
347:. Cell culturing on paper-based microfluidic devices is accomplished either by encapsulating cells in a
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and sample volume requirement, however using open microfluidic channels adds the benefit of removing
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The use of conventional microfluidic devices for cell studies has already improved upon the
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1077:"Rapid Prototyping of Arrayed Microfluidic Systems in Polystyrene for Cell-Based Assays"
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of small biological molecules from cell culturing samples as well as the release of
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Malboubi, Majid; Jayo, Asier; Parsons, Maddy; Charras, Guillaume (August 2015).
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can be used to create microfluidic devices by embossing and bonding methods,
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Boedicker, James Q.; Vincent, Meghan E.; Ismagilov, Rustem F. (2009-07-27).
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Schneider, Thomas; Kreutz, Jason; Chiu, Daniel T. (2013-03-15).
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cells, air exposure to is essential for developing the lungs.
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1245:"Three-Dimensional Paper-Based Model for Cardiac Ischemia"
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578:"The Potential Impact of Droplet Microfluidics in Biology"
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to monitor cellular interactions or complex populations.
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229:can be employed in the multidimensional
189:of all important aspects of the article.
1303:Chinese Journal of Analytical Chemistry
746:Angewandte Chemie International Edition
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185:Please consider expanding the lead to
96:"Cell culturing in open microfluidics"
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1081:Analytical Chemistry
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316:Polydimethylsiloxane
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329:polystyrene
300:fluorinated
1337:Categories
371:References
320:adsorption
277:Cells and
107:newspapers
74:references
36:improve it
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443:: 42–45.
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353:cellulose
324:oligomers
195:July 2019
179:summarize
137:July 2019
42:talk page
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365:hydrogel
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279:proteins
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