Abstract

Diamond-like carbon (DLC) films were synthesized on a p-type silicon wafer using radio-frequency plasma composed of a mixture of Ar and C2H2 (ratio of 7 to 28). NH3 plasma treatment of as-grown DLC substrate was carried out to generate surface-terminal amino groups while oxidation of as-grown DLC was performed in O2 plasma. X-ray photoelectron spectroscopy (XPS) was used to characterize the different surface functions formed on DLC surfaces. Water contact angle measurements indicate different wetbility of modified surfaces. The cell (Mouse MC3T3-E1 pre-osteoblasts) morphology and proliferation were monitored to evaluate the biocompatibility of the modified DLC surfaces. A cell count kit-8 (CCK-8 Beyotime) was employed to determine quantitatively the viable pre-osteoblasts. The cell viability assay shows that osteoblast proliferation are improved on NH3 and O2 plasma-treated DLC surface after culturing for 1day, 2days and 3 days. The cell-surface interactions are studied by fluorescence microscopy. There are more osteoblasts as well as better spreading on the aminated and oxidized surfaces after culturing for 3 days. In summary, compared to the as-grown sample, the modified DLC shows better biocompatibility.

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