The utility of employing a variable duty cycle pulsed plasma polymerization technique to control film chemistry during plasma depositions is examined using allyl alcohol as monomer gas. Large scale progressive variations in film composition are observed with sequential changes in the plasma duty cycles employed, all other plasma variables being held constant. In particular, the −OH functionality of the monomer is increasingly retained in the plasma generated thin films as the radio frequency duty cycle is lowered. Fourier transform infrared and X-ray photoelectron spectroscopic analyses of the films obtained reveal that excellent film chemistry control is achieved during plasma polymerization of this monomer. The surface density controllability of functional groups, coupled with a gradient layering technique described herein to improve film adhesion to substrate surfaces, provides ideal opportunities for molecular tailoring of surfaces via subsequent derivatization reactions.

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Plasma-assisted polymerization of maleic anhydride has been investigated under different experimental conditions. Significant variations in the film chemical structure and the film properties were obtained using pulsed plasma depositions operated at different duty cycles. The film chemical structures were obtained using X-ray photoelectron spectroscopy (XPS) and Fourier transform infra red spectroscopy (FT-IR). Surface derivatization reactions using decylamine and benzylamine were used to demonstrate their surface reactivity toward nucleophilic moieties and to change the surface free energy of the plasma polymer films, all of which are of particular interest for future applications in the attachment of biological molecules and cells. A method of substrate pretreatment was developed to ensure reliable binding between the substrate and the plasma polymer film in aqueous solution. Impedance spectroscopy was used to monitor polymer film changes in aqueous media. The hydrated films showed some resemblance to polyelectrolyte films and a clear correlation could be observed between the density of anhydride groups and the behavior of the films in solution.

Photocatalyzed TiO 2 nanoparticles have been shown to eradicate cancer cells. However the required in situ introduction of UV light limits the use of such a therapy in patients. In the present study, the non-photocatalyic anti-cancer effect of surface functionalized TiO 2 was examined. Nanoparticles bearing -OH, -NH2, or -COOH surface groups, were tested for their effect on in vitro survival of several cancer and control cell lines. The cells tested included B16F10 melanoma, Lewis lung carcinoma (LLC), JHU prostate cancer cells, and 3T3 fibroblasts. Cell viability was observed to depend on particle concentrations, cell types, and surface chemistry. Specifically, -NH 2 and -OH groups exhibited significantly higher toxicity than -COOH. Microscopic and spectrophotometric studies revealed nanoparticle-mediated cell membrane disruption leading to cell death. The results suggest that functionalized TiO 2 , and presumably other nanoparticles, may be surface engineered for targeted cancer therapy.

The direct plasma-induced deposition of tri(ethylene glycol) monoallyl ether is reported. RF plasma polymerization of this monomer was carried out under both continuous wave (CW) and pulsed plasma operation. The major focus of this work was optimization of the degree of retention of the C-O-C bonds of the starting monomer during the deposition process. This successfully was accomplished using low RF power during the CW runs and low RF duty cycles during the pulsed plasma experiments. Spectroscopic analysis of the plasma films revealed a strong dependence of film composition on the RF power and duty cycles employed. In particular, an unusually high level of film chemistry compositional control was demonstrated for the pulsed plasma studies, with film composition varying in a steady, progressive fashion with sequential changes in the ratios of plasma on to plasma off times. This film chemistry controllability is demonstrated despite the relatively low volatility of the starting monomer. The utility of this plasma deposition approach in introducing polyethylene oxide (PEO) structures on solid substrates was evaluated via protein adsorption studies. Radiolabeled bovine albumin adsorption was studied on plasma-modified poly(ethylene teraphthalate) (PET) substrates. Dramatic reductions in both initial adsorption and retention of this protein were observed on PET samples having maximal PEO content relative to its adsorption on untreated PET surfaces. Good stability and adhesion of the plasma films to the underlying PET substrates were observed, as evidenced from prolonged immersion of plasma-treated surfaces in aqueous solution. Overall, the results obtained from the present work provide additional support for the utility of one-step plasma process to reduce biological fouling of surfaces via deposition of PEO surface units.

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Implant-mediated fibrotic reactions are detrimental to the performance of encapsulated cells, implanted drug release devices and sensors. To improve the implant function and longevity, research has emphasized altering cellular responses. Although material surface functional groups have been shown to be potent in affecting cellular activity in vitro and short term in vivo responses, these groups appear to have little influence on long-term in vivo fibrotic reactions, possibly as a result of insufficient interactions between recruited host cells and functional groups on the implants. To maximize the influence of functionality on cells, and to mimic drug release microspheres, functionalized micron-sized particles were created and tested for their ability in modulating tissue responses to biomaterial implants. In this work, the surfaces of polypropylene particles were controllably coated with four different functional groups, specifically –OH, -NH2, -CFx and –COOH, using a radio frequency glow discharge plasma polymerization technique. The effect of these surface functionalities on host tissue responses were then evaluated using a mice subcutaneous implantation model. Major differences were observed in contrasting tissue response to the different chemistries. Surfaces with –OH and –NH2 surface groups induced the thickest fibrous capsule accompanied with the greatest cellular infiltration into the implants. In contrast, surfaces with –CFx and –COOH exhibited the least inflammatory/fibrotic responses and cellular infiltrations. The present results clearly demonstrate that, by increasing the available functionalized surface area and spatial distribution, the effect of surface chemistry on tissue reactivity can be substantially enhanced.

The attachment of fibrinogen, bovine serum albumin, and immunoglobulin on continuous wave (CW) and pulsed plasma polymerized di(ethylene glycol) monovinyl ether was studied using surface plasmon resonance (SPR) spectroscopy and waveguide mode spectroscopy (WaMS). Structural analysis of the films was carried out using Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy. Plasma conditions employed during depositions produced significant differences in the chemical and physical properties of the resultant polymer films. Films deposited under CW and higher plasma duty cycles showed relatively high refractive indices (n > 1.57) and essentially a constant thickness if immersed in aqueous buffer solutions and exhibited a high adsorption affinity for proteins. In contrast, films produced under lower plasma duty cycles were of lower refractive index (n < 1.4), exhibited significant swelling if immersed in aqueous buffer, and were extremely effective in preventing protein adsorption. The SPR and WaMS data suggest that the relatively non-cross-linked films produced at the lower duty cycles exhibit hydrogel-like behavior when immersed in aqueous solutions. It is believed that these hydrated films are responsible for the remarkably effective nonfouling properties of the films deposited at low duty cycles. The relationship between film structure, polymer stability in aqueous buffer, and protein binding affinities are discussed.