5468638 Cell culture insert

1997 ◽  
Vol 15 (1) ◽  
pp. 117-118
1992 ◽  
Vol 20 (1) ◽  
pp. 138-143
Author(s):  
Maria Carrara ◽  
Lorenzo Cima ◽  
Roberto Cerini ◽  
Maurizio Dalle Carbonare

A method has been developed whereby cosmetic products which are not soluble in water or in alcohol can be brought into contact with cell cultures by being placed in a cell culture insert, which is then placed in the cell culture well. Preliminary experiments were carried out with L929 cells, and cytotoxicity was evaluated by measuring neutral red uptake and the total protein content of treated cultured cells. Encouraging results were obtained in comparisons of three cosmetic emulsions and of one emulsion containing a range of concentrations of two preservatives, Kathon CG and Bronopol.


2004 ◽  
Vol 4 (2) ◽  
pp. 88
Author(s):  
Kee Won Kim ◽  
Suk Young Park ◽  
Kyung Bock Lee ◽  
Hyun-su Kim

2017 ◽  
Vol 7 ◽  
pp. 52-60 ◽  
Author(s):  
Shoichiro Sumi ◽  
Masako Kawagoe ◽  
Rie Abe ◽  
Goichi Yanai ◽  
Kai-Chiang Yang ◽  
...  

2019 ◽  
Vol 48 (2) ◽  
pp. 99-108
Author(s):  
Selma Giorgio ◽  
Pedro Henrique Gallo-Francisco

The cell culture insert system is a culturing system for the study of contact-independent cellular communication. Leishmaniasis is a neglect tropical disease with no vaccines and the availabledrugs present toxic side effects. Studies on Leishmania interaction with host macrophages aim to develop strategies for parasite control and drug development. The purpose of this study was to evaluate the effects of interaction between non-infected and L. amazonensis-infected human macrophages, by using the cell culture system. The results showed that the infection index was reduced by 56.2% as compared to controls only when infected macrophages were inserted on both sides of the Transwell membranes. An improvement in macrophage viability was also observed in this cell culture. The levels of interleukin-1β, an inflammatory cytokine, and nitric oxide, a microbicidal molecule, did not increase in L. amazonensis-infected macrophagecultures in the Transwell system; thus other soluble factors were responsible for parasite control.


2005 ◽  
Vol 2005 ◽  
pp. 39-39
Author(s):  
H.R. M ◽  
M.T. Rose ◽  
H. Aso ◽  
W. Haresign ◽  
B. Davies

The aim was to establish a representative model of the bovine mammary gland in order to underpin applied research in mammary gland development and lactation. Cell culture insert methodology is currently being utilized in place of a three dimensional culture system, the shortcomings of which have been discussed elsewhere (McConochie et al., 2004). Cell culture insert methodology offers a promising alternative, with the potential to recreate in vitro a polarised epithelial layer. Previously it has been shown that on collagen I coated inserts, ABERMEC are able to synthesise and secrete mammary specific proteins in the apparent absence of the key mediators laminin and prolactin. It was hypothesised that undefined factors in serum were a possible cause for this phenomenon.


Micromachines ◽  
2021 ◽  
Vol 12 (11) ◽  
pp. 1431
Author(s):  
Takeo Shimasaki ◽  
Satoko Yamamoto ◽  
Risa Omura ◽  
Kagenori Ito ◽  
Yumiko Nishide ◽  
...  

Microfluidics is applied in biotechnology research via the creation of microfluidic channels and reaction vessels. Filters are considered to be able to simulate microfluidics. A typical example is the cell culture insert, which comprises two vessels connected by a filter. Cell culture inserts have been used for years to study cell-to-cell communication. These systems generally have a bucket-in-bucket structure and are hereafter referred to as a vertical-type co-culture plate (VTCP). However, VTCPs have several disadvantages, such as the inability to simultaneously observe samples in both containers and the inability of cell-to-cell communication through the filters at high cell densities. In this study, we developed a novel horizontal-type co-culture plate (HTCP) to overcome these disadvantages and confirm its performance. In addition, we clarified the migration characteristics of substances secreted from cells in horizontal co-culture vessels. It is generally assumed that less material is exchanged between the horizontal vessels. However, the extracellular vesicle (EV) transfer was found to be twice as high when using HTCP. Other merits include control of the degree of co-culture via the placement of cells. We believe that this novel HTCP container will facilitate research on cell-to-cell communication in various fields.


2021 ◽  
Author(s):  
Prasoon Kumar ◽  
Dhaval Kedaria ◽  
Chinmaya Mahapatra ◽  
M Monisha ◽  
Kaushik Chatterjee

Engineered platforms for culturing cells of the skin and other epithelial tissues are useful for the regeneration and development of in vitro tissue models used in drug screening. Recapitulating the...


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