NanoPADs and nanoFACEs: an optically transparent nanopaper-based device for biomedical applications

Lab on a Chip ◽  
2020 ◽  
Vol 20 (18) ◽  
pp. 3322-3333
Author(s):  
Binbin Ying ◽  
Siwan Park ◽  
Longyan Chen ◽  
Xianke Dong ◽  
Edmond W. K. Young ◽  
...  

A highly transparent nanopaper-based microfluidic device for chemical/biosensing and cell culture, which is branded as nanopaper-based analytical devices (nanoPADs) and nanofibrillated adherent cell-culture platforms (nanoFACEs).

2014 ◽  
Vol 8 (1) ◽  
pp. 016503 ◽  
Author(s):  
Angela R. Dixon ◽  
Shrinidhi Rajan ◽  
Chuan-Hsien Kuo ◽  
Tom Bersano ◽  
Rachel Wold ◽  
...  

1999 ◽  
Vol 176 (1) ◽  
pp. 235-240
Author(s):  
Philippe Lawton ◽  
Carine Hejl ◽  
Marie-Elisabeth Sarciron ◽  
Roselyne Mancassola ◽  
Muriel Naciri ◽  
...  

Pharmaceutics ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 229 ◽  
Author(s):  
Dongjin Lee ◽  
Chaenyung Cha

Tumor spheroids are considered a valuable three dimensional (3D) tissue model to study various aspects of tumor physiology for biomedical applications such as tissue engineering and drug screening as well as basic scientific endeavors, as several cell types can efficiently form spheroids by themselves in both suspension and adherent cell cultures. However, it is more desirable to utilize a 3D scaffold with tunable properties to create more physiologically relevant tumor spheroids as well as optimize their formation. In this study, bioactive spherical microgels supporting 3D cell culture are fabricated by a flow-focusing microfluidic device. Uniform-sized aqueous droplets of gel precursor solution dispersed with cells generated by the microfluidic device are photocrosslinked to fabricate cell-laden microgels. Their mechanical properties are controlled by the concentration of gel-forming polymer. Using breast adenocarcinoma cells, MCF-7, the effect of mechanical properties of microgels on their proliferation and the eventual spheroid formation was explored. Furthermore, the tumor cells are co-cultured with macrophages of fibroblasts, which are known to play a prominent role in tumor physiology, within the microgels to explore their role in spheroid formation. Taken together, the results from this study provide the design strategy for creating tumor spheroids utilizing mechanically-tunable microgels as 3D cell culture platform.


Tumor Biology ◽  
2016 ◽  
Vol 37 (9) ◽  
pp. 12359-12370 ◽  
Author(s):  
Javier de la Rosa ◽  
Ander Sáenz Antoñanzas ◽  
Mehdi H. Shahi ◽  
Bárbara Meléndez ◽  
Juan A. Rey ◽  
...  

2019 ◽  
Vol 22 (1) ◽  
Author(s):  
Ashkan YekrangSafakar ◽  
Katie M. Hamel ◽  
Ali Mehrnezhad ◽  
Jangwook P. Jung ◽  
Kidong Park

Nanomaterials ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1765 ◽  
Author(s):  
Dedy Septiadi ◽  
Laura Rodriguez-Lorenzo ◽  
Sandor Balog ◽  
Miguel Spuch-Calvar ◽  
Giovanni Spiaggia ◽  
...  

The overt hazard of carbon nanotubes (CNTs) is often assessed using in vitro methods, but determining a dose–response relationship is still a challenge due to the analytical difficulty of quantifying the dose delivered to cells. An approach to accurately quantify CNT doses for submerged in vitro adherent cell culture systems using UV-VIS-near-infrared (NIR) spectroscopy is provided here. Two types of multi-walled CNTs (MWCNTs), Mitsui-7 and Nanocyl, which are dispersed in protein rich cell culture media, are studied as tested materials. Post 48 h of CNT incubation, the cellular fractions are subjected to microwave-assisted acid digestion/oxidation treatment, which eliminates biological matrix interference and improves CNT colloidal stability. The retrieved oxidized CNTs are analyzed and quantified using UV-VIS-NIR spectroscopy. In vitro imaging and quantification data in the presence of human lung epithelial cells (A549) confirm that up to 85% of Mitsui-7 and 48% for Nanocyl sediment interact (either through internalization or adherence) with cells during the 48 h of incubation. This finding is further confirmed using a sedimentation approach to estimate the delivered dose by measuring the depletion profile of the CNTs.


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