Abstract
Drug-loaded mono- and multilayer composite membranes were prepared. The composites, based on nano-fibrillated bacterial cellulose, nano-powdered bacterial cellulose, and polyvinyl alcohol, all biocompatible and biodegradable, were characterized in terms of basic factors related to drug diffusivity and mass transfer: swelling ability, water solubility, and water vapor permeability. Tetracycline hydrochloride was used in this case as drug model. Drug release was evaluated in an aqueous environment for two concentration levels of the antibiotic, and mathematical modeling was applied to fit experimental data. Tetracycline release was influenced by a membranes’ structure, layers’ composition, and by a membranes’ thickness. Bacterial cellulose nanofibrils proved to be the key factor in achieving suitable drug release profiles. Thus, sustained antibiotic delivery was obtained for several days in the case of multilayer composites. The composites proved drug stability and antibacterial efficiency before and after TC-HCl continuous release for several days.
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