In vitro cytotoxicity assessment using three-dimensional cell cultures of MCF10A cells

2013 ◽  
Vol 221 ◽  
pp. S144
Author(s):  
J.P. Miranda ◽  
M. Cipriano ◽  
A.S. Fernandes ◽  
M. Castro ◽  
N.G. Oliveira
Cytotherapy ◽  
2021 ◽  
Vol 23 (5) ◽  
pp. S145
Author(s):  
S. Kress ◽  
D. Egger ◽  
C. Kasper

1999 ◽  
Vol 25 (1) ◽  
pp. 24-29 ◽  
Author(s):  
Gottfried Schmalz ◽  
Uta Schuster ◽  
Katja Nuetzel ◽  
Helmut Schweikl

Author(s):  
Alessandra Silvestri ◽  
Dirk Schumacher ◽  
Maxine Silvestrov ◽  
Reinhold Schäfer ◽  
Christoph Reinhard ◽  
...  

2021 ◽  
pp. 100379
Author(s):  
Javier Munoz-Garcia ◽  
Camille Jubelin ◽  
Aurélie Loussouarn ◽  
Matisse Goumard ◽  
Laurent Griscom ◽  
...  

Open Medicine ◽  
2020 ◽  
Vol 15 (1) ◽  
pp. 249-253
Author(s):  
Marta Bochynska-Czyz ◽  
Patrycja Redkiewicz ◽  
Hanna Kozlowska ◽  
Joanna Matalinska ◽  
Marek Konop ◽  
...  

AbstractThree-dimensional (3D) cell cultures were created with the use of fur keratin associated proteins (F-KAPs) as scaffolds. The procedure of preparation F-KAP involves combinations of chemical activation and enzymatic digestion. The best result in porosity and heterogeneity of F-KAP surface was received during pepsin digestion. The F-KAP had a stable structure, no changes were observed after heat treatment, shaking and washing. The 0.15-0.5 mm fraction had positive effect for formation of 3D scaffolds and cell culturing. Living rat mesenchymal cells on the F-KAP with no abnormal morphology were observed by SEM during 32 days of cell culturing.


Tumor Biology ◽  
2010 ◽  
Vol 32 (3) ◽  
pp. 469-479 ◽  
Author(s):  
Jianhua Tang ◽  
Jiefeng Cui ◽  
Rongxin Chen ◽  
Kun Guo ◽  
Xiaonan Kang ◽  
...  

2016 ◽  
Vol 54 (2) ◽  
Author(s):  
Ana Ljevar ◽  
◽  
Natka Ćurko ◽  
Marina Tomašević ◽  
Kristina Radošević ◽  
...  

2017 ◽  
Vol 5 (10) ◽  
pp. 2106-2113 ◽  
Author(s):  
Sasha Cai Lesher-Pérez ◽  
Ge-Ah Kim ◽  
Chuan-hsien Kuo ◽  
Brendan M. Leung ◽  
Sanda Mong ◽  
...  

Oxygen measurements in different microtissue culture environments were accomplished with the use of phase fluorimetry on dispersible oxygen microsensors.


Carbon ◽  
2008 ◽  
Vol 46 (11) ◽  
pp. 2-3
Author(s):  
Hong-mei Han ◽  
Gary J. Phillips ◽  
Sergey V. Mikhalovsky ◽  
Andrew W. Lloyd

1997 ◽  
Vol 272 (5) ◽  
pp. C1507-C1512 ◽  
Author(s):  
F. J. Romero ◽  
D. Zukowski ◽  
W. Mueller-Klieser

The cellular glutathione (GSH) content of two- and three-dimensional cell cultures of V79 hamster lung cells has been studied. As previously described, cells in monolayer cultures show a decrease in GSH when they reach the confluent state. Three-dimensional cell cultures (multicell spheroids) allow a smoother transition from the initial proliferating to the nonproliferating status, and they show a central area of necrosis when a certain diameter is reached. Cellular GSH content in spheroids is variable throughout the culturing period: 1) GSH content (expressed per mg protein) is lower in spheroids with central necrotic areas than in smaller spheroids without necrosis, and 2) results expressed per cell number show a sharp increase around the diameter where necrosis appears. Once a relatively large necrotic area has been established, GSH decreases again to approximately the prenecrotic level. Interestingly, this GSH "peak" is not dependent on the time in culture but on the spheroid size. Acute hypoxia occurs in central areas of spheroids at a much higher size range than those described herein. Thus we suggest a combination of factors, which may include oxidative stress among others, as the explanation for these cellular GSH variations.


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