Fabrication of Microfiber-Templated Microfluidic Chips with Microfibrous Channels for High Throughput and Continuous Production of Nanoscale Droplets

2022 ◽  
pp. 127-134
Author(s):  
Guk-Young Ahn ◽  
Inseong Choi ◽  
Minju Song ◽  
Soo Kyung Han ◽  
Kangho Choi ◽  
...  
Micromachines ◽  
2020 ◽  
Vol 11 (3) ◽  
pp. 297 ◽  
Author(s):  
Kena Song ◽  
Guoqiang Li ◽  
Xiangyang Zu ◽  
Zhe Du ◽  
Liyu Liu ◽  
...  

Microfluidic systems have been widely explored based on microfluidic technology, and it has been widely used for biomedical screening. The key parts are the fabrication of the base scaffold, the construction of the matrix environment in the 3D system, and the application mechanism. In recent years, a variety of new materials have emerged, meanwhile, some new technologies have been developed. In this review, we highlight the properties of high throughput and the biomedical application of the microfluidic chip and focus on the recent progress of the fabrication and application mechanism. The emergence of various biocompatible materials has provided more available raw materials for microfluidic chips. The material is not confined to polydimethylsiloxane (PDMS) and the extracellular microenvironment is not limited by a natural matrix. The mechanism is also developed in diverse ways, including its special physical structure and external field effects, such as dielectrophoresis, magnetophoresis, and acoustophoresis. Furthermore, the cell/organ-based microfluidic system provides a new platform for drug screening due to imitating the anatomic and physiologic properties in vivo. Although microfluidic technology is currently mostly in the laboratory stage, it has great potential for commercial applications in the future.


2018 ◽  
Vol 6 (13) ◽  
pp. 3451-3458 ◽  
Author(s):  
Youngkwang Kim ◽  
Sangbae Yu ◽  
Jaeseoung Park ◽  
Daseob Yoon ◽  
Amir Masoud Dayaghi ◽  
...  

Here, we demonstrate the scalable and continuous production of large coatings with thermochromic VO2 nanoparticles for “smart” windows.


2008 ◽  
Vol 29 (24) ◽  
pp. 5055-5060 ◽  
Author(s):  
Linfen Yu ◽  
Huaiqing Huang ◽  
Xiuling Dong ◽  
Dapeng Wu ◽  
Jinhua Qin ◽  
...  

2017 ◽  
Vol 156 ◽  
pp. 349-357 ◽  
Author(s):  
Mariano Michelon ◽  
Davi Rocha Bernardes Oliveira ◽  
Guilherme de Figueiredo Furtado ◽  
Lucimara Gaziola de la Torre ◽  
Rosiane Lopes Cunha

2018 ◽  
Vol 10 (2) ◽  
pp. 025008 ◽  
Author(s):  
Mao Mao ◽  
Jiankang He ◽  
Yongjie Lu ◽  
Xiao Li ◽  
Tianjiao Li ◽  
...  

2015 ◽  
Vol 9 (4) ◽  
pp. 044116 ◽  
Author(s):  
Arjen M. Pit ◽  
Riëlle de Ruiter ◽  
Anand Kumar ◽  
Daniel Wijnperlé ◽  
Michèl H. G. Duits ◽  
...  

2017 ◽  
Vol 11 (2) ◽  
pp. 024118 ◽  
Author(s):  
Jeremy M. Schieferstein ◽  
Ashtamurthy S. Pawate ◽  
Chang Sun ◽  
Frank Wan ◽  
Paige N. Sheraden ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
H. B. Atakan ◽  
R. Xiang ◽  
M. Cornaglia ◽  
L. Mouchiroud ◽  
E. Katsyuba ◽  
...  

Abstract The nematode Caenorhabditis elegans is a suitable model organism in drug screening. Traditionally worms are grown on agar plates, posing many challenges for long-term culture and phenotyping of animals under identical conditions. Microfluidics allows for ‘personalized’ phenotyping, as microfluidic chips permit collecting individual responses over worms’ full life. Here, we present a multiplexed, high-throughput, high-resolution microfluidic approach to culture C. elegans from embryo to the adult stage at single animal resolution. We allocated single embryos to growth chambers, for observing the main embryonic and post-embryonic development stages and phenotypes, while exposing worms to up to 8 different well-controlled chemical conditions. Our approach allowed eliminating bacteria aggregation and biofilm formation-related clogging issues, which enabled us performing up to 80 hours of automated single worm culture studies. Our microfluidic platform is linked with an automated phenotyping code that registers organism-associated phenotypes at high-throughput. We validated our platform with a dose-response study of the anthelmintic drug tetramisole by studying its influence through the life cycle of the nematodes. In parallel, we could observe development effects and variations in single embryo and worm viability due to the bleaching procedure that is standardly used for harvesting the embryos from a worm culture agar plate.


Lab on a Chip ◽  
2020 ◽  
Vol 20 (13) ◽  
pp. 2354-2363 ◽  
Author(s):  
Tomoko Gowa Oyama ◽  
Kotaro Oyama ◽  
Mitsumasa Taguchi

We have developed a high-throughput method for obtaining hydrophilic, rigid, low-absorption/adsorption, and sterilized multi-layer 3D integrated PDMS microfluidic chips simply by applying electron beam or γ-ray irradiation to stacked PDMS layers.


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