Up till now, chitosan has confirmed its versatile application in skin, cartilage and bone tissue engineering, as well as in drug delivery applications. This study is focused on enzymatic degradation of porous chitosan structures usually designed for mentioned purposes. In vitro degradation was monitored during four weeks of incubation at physiological temperature and in two different media, phosphate buffer saline solution and water.The scaffolds were characterised before and after enzymatic degradation using scanning electron microscopy and infrared spectroscopy with Fourier transformations (FTIR). According to the gravimetric analysis, higher weight loss of chitosan scaffolds was observed in buffered medium with respect to the water. The results implied that the total weight loss obtained in buffer involves physical dissolution of chitosan and lysozyme cleavage of glycoside bond. Importantly, FTIR identification of chitosan scaffolds after enzymatic degradation indicated the absence of lysozyme activity in water, indicating that weight loss is a result of the chitosan dissolution. This finding greatly impacts design of degradation experiments and characterisation of degradation behaviour of chitosan-based materials utilised as implants or drug delivery systems.

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Chitosan-based nano- and microspheres have shown great potential in a broad range of applications, including drug delivery, bone tissue engineering, wastewater treatments, etc. The preparation of uniformly sized spheres with controlled morphology and microstructure is still a challenge. This work investigates the influence of cupric ions (Cu2+) on the size, shape, morphology and stability of electrosprayed chitosan–copper (CHT–Cu2+) complex microspheres, using chitosans with different degrees of deacetylation. The dynamic viscosity of CHT–Cu2+ solutions was measured by Höppler viscometer, while attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) was used for the identification of dried microspheres. The size, shape and morphology of microspheres were analyzed by light microscope and scanning electron microscopy (SEM), while stability of dried microspheres was evaluated in different buffer solutions. The volume ratio of wet and dry microspheres was assessed based on the estimated diameter of microspheres. The higher concentration of Cu2+ ions resulted in a decrease in viscosity of CHT–Cu2+ solutions and volume ratio of prepared microspheres. Changes in the intensities and wave numbers of absorption bands of amino and hydroxyl groups, amide I and amide II suggested that the nitrogen and oxygen atoms in chitosan are coordinating the cupric ions. Micrographs obtained by light microscope and SEM showed that all prepared samples are spherical. The increase of cupric ions concentration changed the topography of microspheres and decreased their size. These results indicated the successful electrospraying of CHT–Cu2+ microspheres with uniform size and good stability in aqueous medium.

Selektivno lasersko sinteriranje (SLS) jedan je od važnijih postupaka 3D ispisa koji se u današnje vrijeme sve više primjenjuju za dobivanje različitih modela. Najvažniji polimerni materijali koji se upotrebljavaju u tom procesu su poliamidi. Značajan nedostatak tog procesa je velika količina otpadnog polimernog praha. Stoga je cilj ovoga rada bio istražiti utjecaj dodatka nanočestica titanijeva dioksida (TiO<sub>2</sub>) na toplinska i mehanička svojstva otpadnog poliamidnog praha (PA 2200). U ovom radu pripremljeni su nanokompoziti PA/TiO2 u rasponu masenog udjela punila 1 – 5 %, postupkom zamješavanja punila u talinu polimera u gnjetilici Brabender. Aglomerati nanopunila vidljivi su na SEM mikrografiji 5 %-tnog PA/TiO<sub>2</sub> nanokompozita. Rezultati diferencijalne pretražne kalorimetrije (DSC) ukazuju na djelovanje nanočestica TiO<sub>2</sub> kao heterogenih nukleacijskih centara. Također, dodatak nanopunila pospješuje stvaranje stabilnijih i uređenijih kristalnih struktura poliamidne matrice. Termogravimetrijskom analizom (TGA) dokazano je da dodatak TiO<sub>2</sub> nanopunila povećava temperaturu početka razgradnje PA matrice, to jest poboljšava toplinsku postojanost PA matrice i neznatno povećava vrijednosti toplinske vodljivosti nanokompozita u odnosu na čistu polimernu matricu. Ispitivanjem mehaničkih svojstava uzoraka uočeno je smanjenje vrijednosti sekantnog modula te neznatne promjene naprezanja i istezanja u točki popuštanja s povećanjem udjela punila u nanokompozitu.

The aim of this work was to prepare bimetallic chitosan microgels with high sphericity and investigate the influences of metal-ion type and content on the size, morphology, swelling, degradation and biological properties of microgels. Amino and hydroxyl groups of chitosan (deacetylation degree, DD, of 83.2% and 96.9%) served as ligands in the Cu2+–Zn2+/chitosan complexes with various contents of cupric and zinc ions. The electrohydrodynamic atomization process was used to produce highly spherical microgels with a narrow size distribution and with surface morphology changing from wrinkled to smooth by increasing Cu2+ ions’ quantity in bimetallic systems for both used chitosans. The size of the bimetallic chitosan particles was estimated to be between 60 and 110 µm for both used chitosans, and FTIR spectroscopy indicated the formation of complexes through physical interactions between the chitosans’ functional groups and metal ions. The swelling capacity of bimetallic chitosan particles decreases as the DD and copper (II) ion content increase as a result of stronger complexation with respect to zinc (II) ions. Bimetallic chitosan microgels showed good stability during four weeks of enzymatic degradation, and bimetallic systems with smaller amounts of Cu2+ ions showed good cytocompatibility for both used chitosans.