We report the development of copolymers based on 2-vinylpyridine with different porosity degrees. The copolymers were quaternized with methyl iodide and acrylonitrile to introduce quaternary ammonium groups on pyridine units. To prepare charge transfer complexes, the unmodified copolymers and their derivatives quaternized were impregnated with iodine. The antibacterial properties of all the polymers were evaluated ranging from of the Escherichia coli strain. The unmodified copolymers did not have antibacterial activity against E.Coli suspensions. The quaternization with methyl iodine and acrylonitrile increased the biocidal performance of these copolymers, but only the copolymer with the lowest porosity modified with methyl iodine showed significant bactericidal action for all E. Coli concentrations. The 2-vinylpiridine copolymers quaternized and impregnated with iodine had higher antibacterial activity than the impregnated ones. The charge transfer complexes derived from the copolymer with the lowest porosity and highest swelling capacity in water had the best bactericidal performance.

We report the development of two copolymers based on 2-vinylpyridine, styrene and divinylbenzene (2Vpy-Sty-DVB) with different porosity degrees. The copolymers were subsequently quaternized with methyl iodide. To prepare charge transfer complexes, the unmodified copolymers and their derivatives quaternized with methyl iodine were impregnated with iodine. The antibacterial properties of the polymers were evaluated in dilutions ranging from 10² to 10(7) cells/mL of the auxotrophic OHd5-K12 Escherichia coli strain. It was possible to obtain materials with complete antibacterial activity even in the highest cell concentrations tested.

A simple method was developed to load a large amount of silver nanoparticles into bacterial cellulose (BC) produced by Gluconacetobacter xylinus in a controlled manner. Due to the high electron-rich oxygen density in the BC macromolecules and the large surface area of the BC nanoporous structure as an effective nanoreactor, the in situ direct metallization technique was successfully used to synthesize Ag nanoparticles with an average diameter of 30 nm and a loading content of at least 5 wt. (%), approximately. This novel procedure provides an easy and economical way to manufacture Ag nanoparticles supported on a porous membrane for various biomedical applications. These composite fibers showed nearly 100% antibacterial activity (elimination of microorganisms) against Escherichia coli because of the presence of the silver nanoparticles.