This paper reports new solid materials based on TEGylated phenothiazine and chitosan, with a high capacity to recover mercury ions from aqueous solutions. They were prepared by hydrogelation of chitosan with a formyl derivative of TEGylated phenothiazine, followed by lyophilization. Their structural and supramolecular characterization was carried out by ¹H-NMR and FTIR spectroscopy, as well as X-ray diffraction and polarized light microscopy. Their morphology was investigated by scanning electron microscopy and their photophysical behaviour was examined by UV/Vis and emission spectroscopy. Swelling evaluation in different aqueous media indicated the key role played by the supramolecular organization for their hydrolytic stability. Mercury recovery experiments and the analysis of the resulting materials by X-ray diffraction and FTIR spectroscopy showed a high ability of the studied materials to bind mercury ions by coordination with the sulfur atom of phenothiazine, imine linkage, and amine units of chitosan.

Due to the critical need for effective wound dressings for the management of burn injuries, this paper focuses on addressing key gaps in infection prevention and control. The study aims to develop advanced nanofibrous dressings based on quaternized chitosan/chitosan, loaded with norfloxacin and modified with 2-formylphenylboronic acid to enhance antimicrobial and antioxidant activity and promote healing. The materials combine beneficial properties of chitosan/quaternized chitosan, such as biocompatibility, biodegradability, and antimicrobial activity. The characterization was performed from structural (NMR, FTIR, UV-Vis spectroscopy and thermogravimetric analysis), morphological (SEM, water vapor sorption) and supramolecular points of view (X-Ray Diffraction and Polarized Microscopy). Essential properties for wound dressings were evaluated and proved excellent performances, such as Young's modulus up to 1250 MPa, swelling capacity till 6 g/g, radical scavenging activity of 70 % and enzymatic degradability till 53 % in 21 days. The fibers presented antibacterial properties, reflected by high inhibition zones against Escherichia coli (40 mm) and Staphylococcus aureus (34 mm) and antifungal activity against Candida glabrata (15 mm). Preliminary studies demonstrated the in vitro safety of the materials on Human Gingival Fibroblasts, while in vivo experiments on Wistar rats confirmed the biocompatibility of the materials, emphasizing their potential as effective wound dressings for burns.

The paper reports about binary chitosan/quaternized chitosan nanofibers obtained by direct electrospinning of their solution, without using co-spinning polymers. Both quaternary salts, N,N,N-trimethyl chitosan chloride and N-(2-hydroxyl) propyl-3-trimethyl ammonium chitosan chloride, were used in the electrospinning process and provided nanofibers with a mean diameter lower than 100 nm. A morphological evaluation of the nanofibers prepared with quaternized chitosan and chitosan of different molecular weights indicated that chitosan of lower molecular weight yielded fibers of higher diameter, due to the necessity to increase the concentration of the electrospinning solution in order to reach chain entanglement. Polarized light microscopy suggested that the fibers were semicrystalline in nature, in line with the ability of the macromolecular chains to align in an electrical field. Furthermore, the investigation of the antimicrobial and antifungal activities against relevant gram-positive and gram-negative bacteria, as well as yeast strains, revealed the strong effects of the nanofibers, improved by the presence of quaternary chitosan and the lower diameter of the fibers.

This study aimed to investigate the behavior of chitosan/quaternized chitosan fibers in media mimicking wound exudates to understand their capacities as wound dressing. Fiber analysis of the fibers using dynamic vapor sorption proved their ability to adsorb moisture up to 60% and then to desorb it as a function of humidity, indicating their outstanding breathability. Dissolution analyses showed that quaternized chitosan leached from the fibers in water and PBS, whereas only small portions of chitosan were solubilized in water. In media containing lysozyme, the fibers degraded with a rate determined by their composition and pH, reaching a mass loss of up to 47% in media of physiologic pH. Notably, in media mimicking the wound exudate during healing, they adsorbed moisture even when their mass loss due to biodegradation was high, whereas they were completely degraded in the media of normal tissues, indicating bioabsorbable dressing capacities. A mathematical model was constructed, which characterized the degradation rate and morphology changes of chitosan/quaternized chitosan fibers through analyses of dynamics in scale space, using the Theory of Scale Relativity. The model was validated using experimental data, making it possible to generalize it to the degradation of other biopolymeric systems that address wound healing.

The present study reported the obtention of xerogels based on chitosan and citral and their use as materials for mercury ion recovery from aqueous solutions, this being a serious problem related to the environment. The systems were prepared by the acid condensation of chitosan with citral, followed by the lyophilization of the resulting hydrogels, in order to obtain highly porous solid materials. The structural, morphological and supramolecular characterization of the systems was performed using ¹H-NMR and FTIR spectroscopy, scanning electron microscopy and wide-angle X-ray diffraction. The ability of the obtained materials to be used for the recovery of mercury from aqueous solutions revealed the high potential of the xerogels to be used in this sense, the analysis of the materials post mercury absorption experiments revealing that this ability is predominantly conferred by the imine linkages which act as coordinating moieties for mercury ions.