Wound healing is a complex process, and propolis, a natural resin with antimicrobial, anti-inflammatory, and antioxidant properties, emerges as a promising candidate for its treatment. This systematic review analyzed 26 studies on propolis-functionalized biomaterials. Great diversity was observed in materials and incorporation techniques, including direct blending, surface coating, and nanoencapsulation. Mostly based on polysaccharides like chitosan, pectin, and bacterial cellulose, these formulations showed biocompatibility, biodegradability, and promoted inflammation reduction and tissue repair. In vitro assays confirmed high biocompatibility (>80% cell viability) and antimicrobial activity, while in vivo studies validated regenerative benefits. Despite their potential, marked heterogeneity in propolis composition (intrinsically variable due to its botanical and geographical origin, and processing methods), coupled with diverse concentrations used and the lack of standardization in assessment methods and results reporting, significantly limits cross-study comparability and reproducibility. Overcoming these challenges requires promoting greater standardization in extraction, characterization, and evaluation protocols, including chemical fingerprinting and more detailed and consistent reporting of findings. Despite these limitations, propolis–polysaccharide systems hold strong clinical potential, with further standardization and well-designed preclinical studies being essential for their effective translation, especially in chronic wound management.

Nosocomial infections are an important health problem and cause of complications and death in hospitalized patients. This problem should be solved from the preventive angle, avoiding the spread of infections by designing disinfection methods based on the photocatalytic activity of semiconductor materials such as tin oxide (SnO₂). The antimicrobial activity of UV light was tested by using inoculation with Candida albicans ATCC10231 on SnO₂ thin films and counting colony forming units (CFU). The interaction of UV light with SnO₂ was analyzed by density functional theory (DFT) and the extension to the Hubbard model (DFT+U) schemes to predict the electron behavior at the subatomic level. After exposure to UV light, C. albicans showed a reduction of 36.5% in viable cells, and when SnO₂ was included, cell viability was reduced by 60.2%. Measurements of the electronic structure obtained by the first-principle calculations under the DFT and DFT+U schemes showed that the O-p orbitals mediate the oxidation process in the bulk semiconductor. By including the surface effects when cleaving the (1 0 0) plane, the three orbitals O-p, Sn-p, and Sn-s are the mediators. SnO₂ films are promising antimicrobial coatings because UV light has a synergic activity with thin films, resulting in faster disinfection.

Postsurgical infections are an important cause of implant failure, and biomaterials such as Chitosan can be used as an antimicrobial coating to address this important problem. Characterization of silver distribution was performed by several methods, including Electron scanning microscopy (SEM), Inductively coupled plasma (ICP), and Infrared spectrometry (IR). Antimicrobial activity was tested against Candida albicans ATCC 10231, Staphylococcus aureus ATCC 29213, Escherichia coli ATCC 25922, and Pseudomonas aeruginosa BAA-1744 ATCC 109246. The inhibition assays showed that Chitosan films inhibited 68% of C. albicans growth and 23.5% of E. coli growth; the rest of the microorganisms did not have any statistically relevant inhibition. E. coli, P. aeruginosa, and C. albicans were completely inhibited in films with 0.25 mg/mL of AgNO₃ and inhibited 82.5% of S. aureus. The mechanism of integration and release of silver in the films was analyzed by the Density Functional Theory (DFT), considering this analysis of geometry optimization as well as infrared spectroscopy. DFT analysis showed that AgNO₃ is not trapped by covalence in chitosan, being a more stable system when it is closer to an OH group. Chitosan films functionalized with antimicrobial compounds are a promising antimicrobial coating for use in biomaterials to prevent postsurgical complications.

The bactericidal effect of electric current has been studied in various microorganisms such as Pseudomonas aeruginosa. The objective of this review is to identify the experimental parameters with the greatest antibacterial effect in the shortest time. Literature search was conducted in the databases PubMed, Science Direct, and Google Scholar. Only original articles published between 2014 and 2023 were included, where the effect of electric current on viability, biofilm formation, and/or antibiotic resistance in P. aeruginosa was analyzed. Quality control criteria considered included specifying control and experimental groups, replicates performed, experimental parameters, and study limitations. Ten studies were included, which involved the strains Xen5, Xen41, PAO1 persistent cells, and PA14. An average reduction of 3.5 log in biofilm formation was observed in the included studies. The electric current parameters that achieved the greatest effect were 500 μA DC with platinum electrodes for 4 days [5.2-5.5 log], 200 μA intermittent with titanium electrodes for 4 days [4.99 log], and 150 ± 60 μA with silver electrodes for 24 h [4 log]. Complete eradication of PAO1 persistent cells was achieved in 1 h with a treatment of 70 μA/cm2 DC followed by 1.5 μg/mL tobramycin for 1 h each. The bactericidal effect of electric current is proportional to the exposure time and current intensity. The electrode material influences the effectiveness of the treatment, possibly because of redox reactions, while differences are observed in the effect on the cell membrane and gene expression when using metallic or carbon electrodes, suggesting differences in the mechanism of action.

Nosocomial infections caused by Candida albicans pose serious challenges to healthcare systems due to their persistence on medical surfaces and resistance to conventional disinfectants. This study evaluates antifungal properties of SnO₂ doped with silver and cuprite nanoparticles and WO₃ thin films, as well as cobalt (CoFe₂O₄) and cobalt–nickel (Co_0.5Ni₀.₅Fe₂O₄) ferrite nanoparticles, activated by ultraviolet C (UVC) radiation, direct electric current (up to 100 V), and magnetic fields. SnO₂ films were synthesized by Spray Pyrolysis and WO₃ by Sputtering deposition, Ferrites nanoparticles by sol–gel, while metallic nanoparticles were synthetized via chemical reduction. Characterization consisted mainly of SEM, TEM, and XRD, and their antimicrobial activity was tested against C. albicans. WO₃ films achieved 86.2% fungal inhibition after 5 min of UVC exposure. SnO₂ films doped with nanoparticles reached 100% inhibition when combined with UVC and 100 V. Ferrite nanoparticles alone showed moderate activity (21.9%–40.4%) but exhibited strong surface adhesion to fungal cells, indicating potential for magnetically guided antifungal therapies. These results demonstrate the feasibility of using multifunctional nanomaterials for rapid, non-chemical disinfection. The materials are low-cost, scalable, and adaptable to hospital settings, making them promising candidates for reducing healthcare-associated fungal infections through advanced surface sterilization technologies.

Background: Developing reliable and cost-effective decellularization methods is critical for advancing tissue engineering and regenerative medicine, particularly in regions with limited access to specialized perfusion systems. Methods: This study standardized a gravity-assisted perfusion protocol for rat liver decellularization, designed to operate without pumps or pressurized equipment. Adult Wistar rat livers were processed through a gravity-driven vascular flushing method and compared with a conventional immersion-based protocol. The resulting scaffolds were evaluated by macroscopic inspection, histological staining (Masson’s trichrome), and residual DNA quantification. Results: The gravity-assisted perfusion method achieved more efficient cellular removal and superior preservation of extracellular matrix (ECM) integrity compared with immersion. Residual DNA levels were 3.7 ng/mg in perfused samples, 209.47 ng/mg in immersed samples, and 331.97 ng/mg in controls, confirming a statistically significant reduction (p < 0.05). Only the perfused group met the accepted threshold for effective decellularization (<50 ng/mg dry tissue). Histological analysis corroborated these findings, showing the absence of nuclei and the preservation of collagen architecture characteristic of a structurally intact ECM. Conclusions: This low-cost, reproducible, and technically simple system enables the generation of high-quality acellular hepatic scaffolds without mechanical pumps. Its accessibility and scalability make it suitable for laboratories with limited infrastructure and educational settings. Moreover, this gravity-assisted approach provides a foundation for future recellularization and preclinical studies aimed at developing bioengineered liver constructs for regenerative and transplant applications.