Investigation of cell culture in microfluidic devices with different bi-layer substrates

2011 ◽  
Vol 88 (8) ◽  
pp. 1693-1697 ◽  
Author(s):  
Jian Shi ◽  
Li Liu ◽  
Yong Chen
Keyword(s):  
Cell Culture ◽  
Microfluidic Devices

Low density cell culture of locust neurons in closed-channel microfluidic devices

2010 ◽  
Vol 56 (8) ◽  
pp. 1003-1009 ◽  
Author(s):  
Katrin Göbbels ◽  
Anja Lena Thiebes ◽  
André van Ooyen ◽  
Uwe Schnakenberg ◽  
Peter Bräunig
Keyword(s):  
Cell Culture ◽  
Microfluidic Devices ◽  
Low Density ◽  
Closed Channel

scholarly journals A Modular Toolkit to Fabricate Microfluidic Devices for 3D Cell Culture and Near Real-time Measurements

2020 ◽  
Author(s):  
Giraso Kabandana ◽  
Adam Michael Ratajczak ◽  
Chengpeng Chen
Keyword(s):  
Cell Culture ◽  
Real Time ◽  
Low Cost ◽  
New Technology ◽  
Microfluidic Channel ◽  
3D Cell Culture ◽  
Microfluidic Devices ◽  
In Vitro Cell Cultures ◽  
Scoring Tools

Microfluidic technology has tremendously facilitated the development of in vitro cell cultures and studies. Conventionally, microfluidic devices are fabricated with extensive facilities by well-trained researchers, which hinders the widespread adoption of the technology for broader applications. Enlightened by the fact that low-cost microbore tubing is a natural microfluidic channel, we developed a series of adaptors in a toolkit that can twine, connect, organize, and configure the tubing to produce functional microfluidic units. Three subsets of the toolkit were thoroughly developed: the tubing and scoring tools, the flow adaptors, and the 3D cell culture suite. To demonstrate the usefulness and versatility of the toolkit, we assembled a microfluidic device and successfully applied it for 3D macrophage cultures, flow-based stimulation, and automated near real-time quantitation with new knowledge generated. Overall, we present a new technology that allows simple, fast, and robust assembly of customizable and scalable microfluidic devices with minimal facilities, which is broadly applicable to research that needs or could be enhanced by microfluidics.

scholarly journals Automation of Three-Dimensional Cell Culture in Arrayed Microfluidic Devices

2011 ◽  
Vol 16 (3) ◽  
pp. 171-185 ◽  
Author(s):  
Sara I. Montanez-Sauri ◽  
Kyung Eun Sung ◽  
John P. Puccinelli ◽  
Carolyn Pehlke ◽  
David J. Beebe
Keyword(s):  
Cell Culture ◽  
Three Dimensional ◽  
Microfluidic Devices ◽  
Dimensional Cell

Micro- and nanometer-scale patterned surface in a microchannel for cell culture in microfluidic devices

2007 ◽  
Vol 390 (3) ◽  
pp. 817-823 ◽  
Author(s):  
Makiko Goto ◽  
Takehiko Tsukahara ◽  
Kiichi Sato ◽  
Takehiko Kitamori
Keyword(s):  
Cell Culture ◽  
Microfluidic Devices ◽  
Nanometer Scale ◽  
Patterned Surface

scholarly journals Aspiration-mediated hydrogel micropatterning using rail-based open microfluidic devices for high-throughput 3D cell culture

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Dohyun Park ◽  
Jungseub Lee ◽  
Younggyun Lee ◽  
Kyungmin Son ◽  
Jin Woo Choi ◽  
...  
Keyword(s):  
Cell Culture ◽  
Capillary Pressure ◽  
Microfluidic Device ◽  
High Throughput ◽  
3D Cell Culture ◽  
Microfluidic Devices ◽  
Cell Types ◽  
Human Organ ◽  
Patterning Technique ◽  
Experimental Yield

AbstractMicrofluidics offers promising methods for aligning cells in physiologically relevant configurations to recapitulate human organ functionality. Specifically, microstructures within microfluidic devices facilitate 3D cell culture by guiding hydrogel precursors containing cells. Conventional approaches utilize capillary forces of hydrogel precursors to guide fluid flow into desired areas of high wettability. These methods, however, require complicated fabrication processes and subtle loading protocols, thus limiting device throughput and experimental yield. Here, we present a swift and robust hydrogel patterning technique for 3D cell culture, where preloaded hydrogel solution in a microfluidic device is aspirated while only leaving a portion of the solution in desired channels. The device is designed such that differing critical capillary pressure conditions are established over the interfaces of the loaded hydrogel solution, which leads to controlled removal of the solution during aspiration. A proposed theoretical model of capillary pressure conditions provides physical insights to inform generalized design rules for device structures. We demonstrate formation of multiple, discontinuous hollow channels with a single aspiration. Then we test vasculogenic capacity of various cell types using a microfluidic device obtained by our technique to illustrate its capabilities as a viable micro-manufacturing scheme for high-throughput cellular co-culture.

scholarly journals Surface modification of PDMS-based microfluidic devices with collagen using polydopamine as a spacer to enhance primary human bronchial epithelial cell adhesion

2020 ◽  
Author(s):  
Mohammadhossein Dabaghi ◽  
Shadi Shahriari ◽  
Neda Saraei ◽  
Kevin Da ◽  
Abiram Chandiramohan ◽  
...  
Keyword(s):  
Cell Culture ◽  
Surface Modification ◽  
Cell Adhesion ◽  
Microfluidic Devices ◽  
Extracellular Matrix Protein ◽  
Shear Stresses ◽  
Bronchial Epithelial ◽  
Ecm Proteins ◽  
Coating Methods ◽  
Organ On A Chip

AbstractPolydimethylsiloxane (PDMS) is a silicone-based synthetic material that is used in various biomedical applications due to its properties, including transparency, flexibility, permeability to gases, and ease of use. Though PDMS facilitates and realizes the fabrication of complicated geometries at the micro and nano scales, it does not optimally interact with cells for adherence and proliferation. Different strategies have been proposed to render PDMS to enhance cell attachment. The majority of these surface modification techniques have been offered for a static cell culture system. However, dynamic cell culture systems such as organ-on-a-chip devices are demanding platforms that recapitulate the complexity of a living tissue microenvironment. For organ-on-a-chip platforms, PDMS surfaces are usually coated by ECM proteins, which occur as a result of physical, weak bonding between PDMS and ECM proteins, and this binding can be degraded when it is exposed to shear stresses. This work reports static and dynamic coating methods to covalently bind collagen within a PDMS-based microfluidic device using polydopamine (PDA). These coating methods were evaluated using water contact angle measurement and atomic force microscopy (AFM) to find the optimum coating conditions. The biocompatibility of collagen-coated PDMS devices was assessed by culturing primary human bronchial epithelial cells (HBECs) in microfluidic devices. It was shown that both PDA coating methods could be used to bind collagen, thereby improving cell adhesion (around three times higher) without showing any discernible difference. These results suggested that such a surface modification can be used to coat an extracellular matrix protein onto PDMS-based microfluidic devices.

scholarly journals 3D printed microfluidic devices for cell culture

2021 ◽  
Vol 4 (s1) ◽  
Author(s):  
Marta Canta ◽  
Désirée Baruffaldi ◽  
Ignazio Roppolo ◽  
Annalisa Chiappone ◽  
Candido F. Pirri ◽  
...  
Keyword(s):  
Cell Culture ◽  
Microfluidic Device ◽  
Microfluidic Devices ◽  
3D Printed ◽  
Biomedical Field ◽  
Printed Materials

A successful application of the 3D printed materials in the biomedical field requires extensive studies to ensure their biocompatibility at every step of the process. Here, different components suitable for cell applications, including a microfluidic device, were 3D printed using common resins and a deep analysis of their biocompatibility and post printed protocols was conducted.

scholarly journals Enhancement of Virus Infection Using Dynamic Cell Culture in a Microchannel

Micromachines ◽  
2018 ◽  
Vol 9 (10) ◽  
pp. 482
Author(s):  
Jeong Kim ◽  
Hye Choi ◽  
Chul Kim ◽  
Hee Jin ◽  
Jae-sung Bae ◽  
...  
Keyword(s):  
Cell Culture ◽  
Virus Infection ◽  
Soft Lithography ◽  
Fluorescent Protein ◽  
Microfluidic Devices ◽  
Petri Dish ◽  
Culture Method ◽  
Dynamic Culture ◽  
Conventional Culture ◽  
Dynamic Cell

With increasing interest in induced pluripotent stem cells (iPSCs) in the field of stem cell research, highly efficient infection of somatic cells with virus factors is gaining importance. This paper presents a method of employing microfluidic devices for dynamic cell culture and virus infection in a microchannel. The closed space in the microchannel provided a better environment for viruses to diffuse and contact cell surfaces to infect cells. The microfluidic devices were fabricated by photolithography and soft lithography. NIH/3T3 fibroblast cells were cultured in the microfluidic device in static and dynamic conditions and compared with the conventional culture method of using Petri dishes. Virus infection was evaluated using an enhanced green fluorescent protein virus as a model. Dynamic culture in the microchannel showed similar growth of cells to that in Petri dish culture, but the virus infection efficiency was four-times higher. The proposed dynamic culture system could be useful in iPSC research by providing efficient virus infection tools.

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