Plasma polymer films as an alternative to (PSS-PAH)n or (PSS-PDADMAC)n films to retain active enzymes in exponentially growing polyelectrolyte multilayers.

Compact and linearly growing polyelectrolyte multilayer films have been used to suppress desorption of drugs, nanoparticles or proteins from underlying polyelectrolyte multilayer films as well as to significantly change their mechanical properties. The polyelectrolyte based capping layers are however cumbersome to deposit and alternative barrier layers offering enzymatic retention in the films as well as permeability to small molecules, for example the substrates of the embedded enzymes, are highly desired. In this article we show that barrier layers made through atmospheric pressure dielectric barrier discharge polymerization of ethylene glycol dimethacrylate offer the opportunity to simultaneously suppress enzyme desorption from the underlying polyelectrolyte multilayer film and to ensure accessibility of the enzymatic substrate. This holds true when the barrier film totally covers the underlying film and as long is not too thick. When the plasma deposited barrier becomes 300 nm thick, the hydrolysis curve of the enzyme presents a lag phase typical of a diffusion-limited process.

One step preparation of plasma based polymer films for drug release.

Among various atmospheric pressure plasma deposition techniques, the so-called "Atmospheric Pressure Plasma Dielectric Barrier Discharges" (APDBD) has recently received a lot of attention due to the easy ignition of a stable discharge and its scalability. In the present work we aim at designing plasma polymer based films for biomedical applications, in which the drug to be released will be directly incorporated in the film during its deposition. Plasma polymer films made of methacrylic acid (MAA) and of ethylene glycol dimethacrylate (EGDMA) were prepared, allowing to obtain smart coatings able to release the molecule of interest, acetaminophen. A combination of different analytic tools shows that the functional groups of the film are well preserved with respect to the monomer structure and that the drug initially put in the gas phase is embedded in the plasma film with its structure being preserved. The physical and chemical characteristics of the elaborated film allowed for the progressive release of acetaminophen by simply dipping the film into a deionized water solution. However only 8% of the acetaminophen present in the monomer mixture could be released slowly in the presence of water. The significance of this result will be discussed.