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Surface plasma functionalization influences macrophage behavior on carbon nanowalls

Year: 2015

Journal: MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, Vol. 48, p 118-125, 20170208

Authors: Ion, Raluca; Vizireanu, Sorin; Stancu, Claudia Elena; Luculescu, Catalin; Cimpean, Anisoara; Dinescu, Gheorghe

Organizations: Univ Bucharest, Dept Biochem & Mol Biol, Bucharest 050095, Romania; Natl Inst Laser Plasma & Radiat Phys, Bucharest 077125, Romania; Leibniz Inst Plasma Sci & Technol INP Greifswald, D-17489 Greifswald, Germany

The surfaces of carbon nanowall samples as scaffolds for tissue engineering applications were treated with oxygen or nitrogen plasma to improve their wettability and to functionalize their surfaces with different functional groups. X-ray photoelectron spectroscopy and water contact angle results illustrated the effective conversion of the carbon nanowall surfaces from hydrophobic to hydrophilic and the incorporation of various amounts of carbon, oxygen and nitrogen functional groups during the treatments. The early inflammatory responses elicited by un-treated and modified carbon nanowall surfaces were investigated by quantifying tumor necrosis factor-alpha and macrophage inflammatory protein-1 alpha released by attached RAW 264.7 macrophage cells. Scanning electron microscopy and fluorescence studies were employed to investigate the changes in macrophage morphology and adhesive properties, while MU assay was used to quantify cell proliferation. All samples sustained macrophage adhesion and growth. In addition, nitrogen plasma treatment was more beneficial for cell adhesion in comparison with un-modified carbon nanowall surfaces. Instead, oxygen plasma functionalization led to increased macrophage adhesion and spreading suggesting a more activated phenotype, confirmed by elevated cytokine release. Thus, our findings showed that the chemical surface alterations which occur as a result of plasma treatment, independent of surface wettability, affect macrophage response in vitro. (C) 2014 Elsevier B.V. All rights reserved.