Fig. 2. PEG-PAM coating can be UV cured directly on to metal surfaces.
a PAM, PEG-SH, and photoinitiator DMPA are dissolved in chloroform. The antibiotic (vancomycin for example) is also dissolved in chloroform. The surfaces (pin or flat slide) are submerged in the coating solution and excess reagents removed by gravity, the surface is then exposed to UV light to induce PEG-PAM coupling. b 3D profilometer scan of PEG-PAM coated titanium surface. c A horizontal and vertical measurement of coating thickness using the 3D profilometer scan reveals a coating thickness of 2 µm. d SEM images of uncoated and PEG-PAM/Vanc coated titanium pins show a change in surface roughness as a result of the coating process. e Multiple layer deposition of PEG-PAM polymer coatings (3 Layers, 5 Layers, and 8 Layers) with increased thickness and increased loading amount of vancomycin (n = 4). f The thickness of 1, 3, 5, 8 layers of PEG-PAM coatings on the titanium surface (n = 1). g In vitro release of vancomycin from single layer PEG-PAM coating (n = 3). h In vitro release of vancomycin from 3 layers PEG-PAM coating (n = 3). Statistics in (e) are an ordinary one-way ANOVA with a Tukey Multiple comparison test. **p = 0.002 and *p = 0.012. Data is plotted showing the Mean and Standard Deviation. Biological replicates derived from independent experiments are shown in each panel as a dot.