4.4 Review

The Evolution of Polystyrene as a Cell Culture Material

期刊

TISSUE ENGINEERING PART B-REVIEWS
卷 24, 期 5, 页码 359-372

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.teb.2018.0056

关键词

polystyrene; surface chemical modification; plasma treatment; custom fabrication; electrospinning; 3D printing

资金

  1. NIST [2014-NIST-MSE-01]
  2. MSCRF/TEDCO Postdoctoral Fellowship [2017-MSCRF-3920]
  3. Maryland Stem Cell Research Fund/TEDCO [2015-MSCRF-1717]
  4. National Institute of Biomedical Imaging and Bioengineering/National Institutes of Health (NIBIB/NIH) Center for Engineering Complex Tissues [P41 EB023833]
  5. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [P41EB023833] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Polystyrene (PS) has brought in vitro cell culture from its humble beginnings to the modern era, propelling dozens of research fields along the way. This review discusses the development of the material, fabrication, and treatment approaches to create the culture material. However, native PS surfaces poorly facilitate cell adhesion and growth in vitro. To overcome this, liquid surface deposition, energetic plasma activation, and emerging functionalization methods transform the surface chemistry. This review seeks to highlight the many potential applications of the first widely accepted polymer growth surface. Although the majority of in vitro research occurs on two-dimensional surfaces, the importance of three-dimensional (3D) culture models cannot be overlooked. The methods to transition PS to specialized 3D culture surfaces are also reviewed. Specifically, casting, electrospinning, 3D printing, and microcarrier approaches to shift PS to a 3D culture surface are highlighted. The breadth of applications of the material makes it impossible to highlight every use, but the aim remains to demonstrate the versatility and potential as both a general and custom cell culture surface. The review concludes with emerging scaffolding approaches and, based on the findings, presents our insights on the future steps for PS as a tissue culture platform.

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