Issue 32, 2016

A multifunctional resealable perfusion chip for cell culture and tissue engineering

Abstract

We describe a multifunctional resealable perfusion chip to mimic the human environment for cell or tissue culture in vitro and to increase the efficiency of culture in this study. To meet the culture requirement of a two-dimensional (2D) submerged cultures and an air–liquid interface perfusion cultures, a multifunctional resealable perfusion chip was designed and fabricated. Human embryonic kidney cells (HEK293T) and human colon carcinoma cells (SW620) were submerged cultured in the chip for 72 h. Cell viability and cell proliferation tests were used to evaluate the performance of the chip. Moreover, an artificial epidermis was developed, and it lasted for 7 days for the submerged culture immortal human keratinocyte (HaCaT) monolayer and 35 days for the air–liquid interface differentiated culture. The artificial epidermis cultured in the chip and in a conventional transwell were evaluated by the Live/Dead Viability/Cytotoxicity kit, histology, and hematoxylin and eosin staining. The stability and the benefits of our resealable chip were demonstrated by culture cells and epidermis tissue. Unlike a conventional static culture, no obvious advantage was observed in the 2D submerged culture of HEK293T and SW620 cells in the chip, but an outstanding advantage was observed in the 2D HaCaT cell culture with high density and a reconstructed epidermis. The cells grew well, and the epidermis was successfully reconstructed. This result implies that our multifunctional chip has great potential in cell culture and tissue engineering applications.

Graphical abstract: A multifunctional resealable perfusion chip for cell culture and tissue engineering

Article information

Article type
Paper
Submitted
18 Dec 2015
Accepted
07 Mar 2016
First published
11 Mar 2016

RSC Adv., 2016,6, 27183-27190

A multifunctional resealable perfusion chip for cell culture and tissue engineering

Q. Lang, Y. Ren, Y. Wu, Y. Guo, X. Zhao, Y. Tao, J. Liu, H. Zhao, L. Lei and H. Jiang, RSC Adv., 2016, 6, 27183 DOI: 10.1039/C5RA27102A

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