Laboratory preparation of plasticware to support cell culture |
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Authors: | J. A. Chinn T. A. Horbett B. D. Ratner |
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Affiliation: | (1) CarboMedics, Austin, Texas, USA;(2) Center for Bioengineering and Department of Chemical Engineering, BF-10, University of Washington, 98195 Seattle, WA, USA |
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Abstract: | Summary Many plastics, including polystyrene and poly(ethylene terephthalate), are unsuitable for cell culture applications as formed because they do not support cell growth. Although cells may attach to these materials, the attached cells typically round up and detach or die after a short time. However, plastics can be made to support normal cell attachment and growth through surface modification by glow discharge processes that produce ionized gas species which react with the surface of the plastic. This article describes radiofrequency glow discharge (RFGD) modification of plastics in the presence of organic vapors such as acetone, methanol and ethylene oxide. These treatments render laboratory plastics amenable to in vitro cell culture. Successful modification is a function of RFGD reaction parameters (position within the reactor, discharge power, system pressure, flow rate, and reaction time), and can be confirmed by electron spectroscopy for chemical analysis (ESCA). Identification by high resolution ESCA of functional groups introduced onto the surface by the RFGD process can be used to correlate cell growth with surface chemistry. A brief discussion of other processes thought to be used for preparation of commercial tissue culture ware is also provided. |
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Keywords: | Cell culture Glow discharge Tissue culture plastic |
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