Fluorohydrocarbon Plasma Functionalization of Polyurethane Surfaces: Bacterial Adhesion and Cell Response

Polyurethanes (PUs) are widely used in biomedical applications; however, their surface properties critically determine bacterial colonization and cell response. In this study, medical-grade PU films were modified using low-pressure C3H2F4 plasma (50 W, 300 s, 0.2 mbar), and the resulting changes in surface chemistry, wettability, topography, bacterial adhesion, and cell compatibility were evaluated. X-ray photoelectron spectroscopy (XPS) analysis confirmed the incorporation of fluorine-containing groups (CF2, CF3) and the appearance of an F 1s signal at ~688.3 eV. Plasma treatment increased the water contact angle from 92.6° ± 5.6° to 97.9° ± 3.1° and elevated the root mean square (RMS) surface roughness (Sq) from 39.0 nm to 77.3 nm. Surface free energy slightly decreased after plasma treatment due to reductions in both polar and dispersive components. Quantitative adhesion assays revealed strain-dependent effects. For S. aureus DSM 4910, S. epidermidis DSM 28319, and P. aeruginosa DSM 22644, no consistent reduction in adhesion was observed on plasma-treated surfaces. In contrast, E. coli DSM 18039 demonstrated significantly higher adhesion on modified PU at all incubation times, reaching 5.96 ± 0.44 logCFU/mL after 240 min compared to 5.05 ± 0.27 log colony-forming units per milliliter (logCFU/mL) on unmodified PU. Fluorescence microscopy confirmed increased surface coverage by E. coli on fluorinated samples. Biocompatibility studies using A549 cells showed no cytotoxic effects. Cell spreading area remained comparable between surfaces (1188.6 vs. 1185.1 µm2; p = 0.958). However, cells on plasma-treated PU exhibited reduced major axis length (38.6 vs. 46.7 µm; p < 0.001) and decreased focal adhesion area (8.88 vs. 10.94 µm2; p = 0.002), indicating moderate alterations in cell morphology without compromised viability. These results demonstrate that C3H2F4 plasma fluorination moderately increases PU hydrophobicity and nanoscale roughness, induces strain-dependent changes in bacterial adhesion—particularly enhancing E. coli colonization—while fully preserving mammalian cell viability and showing no cytotoxic effects of the modified surface.