Document Type
Article
Publication Date
2-21-2019
Abstract
Natural tissues contain highly organized cellular architecture. One of the major challenges in tissue engineering is to develop engineered tissue constructs that promote cellular growth in physiological directionality. To address this issue, micro-patterned polydimethylsiloxane (PDMS) substrates have been widely used in cell sheet engineering due to their low microfabrication cost, higher stability, excellent biocompatibility, and most importantly, ability to guide cellular growth and patterning. However, the current methods for PDMS surface modification either require a complicated procedure or generate a non-uniform surface coating, leading to the production of poor-quality cell layers. A simple and efficient surface coating method is critically needed to improve the uniformity and quality of the generated cell layers. Herein, a fast, simple and inexpensive surface coating method was analyzed for its ability to uniformly coat polydopamine (PD) with or without collagen on micro-grated PDMS substrates without altering essential surface topographical features. Topographical feature, stiffness and cytotoxicity of these PD and/or collagen based surface coatings were further analyzed. Results showed that the PD-based coating method facilitated aligned and uniform cell growth, therefore holds great promise for cell sheet engineering as well as completely biological tissue biomanufacturing.
Publication Title
Bioactive Materials
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Recommended Citation
Sharma, D.,
Jia, W.,
Long, F.,
Pati, S.,
Chen, Q.,
Qyang, Y.,
Lee, B. P.,
Choi, C. K.,
&
Zhao, F.
(2019).
Polydopamine and collagen coated micro-grated polydimethylsiloxane for human mesenchymal stem cell culture.
Bioactive Materials,
4, 142-150.
http://doi.org/10.1016/j.bioactmat.2019.02.002
Retrieved from: https://digitalcommons.mtu.edu/biomedical-fp/43
Version
Publisher's PDF
Publisher's Statement
Article deposited here in compliance with publisher policy. Publisher's version of record: https://doi.org/10.1016/j.bioactmat.2019.02.002