The market trend for pitaya is increasing, although the preservation of the quality of this fruit after the harvest is challenging due to microbial decay, dehydration, and oxidation. In this work, the application of antimicrobial chitosan-based coatings achieved successful postharvest preservation of pitaya (Stenocereus pruinosus) during storage at 10 ± 2 °C with a relative humidity of 80 ± 5%. The solution of cross-linked chitosan with hydroxypropylmethylcellulose with entrapped Neem oil (16 g·L⁻¹) displayed the best postharvest fruit characteristics. The reduction of physiological weight loss and fungal contamination, with an increased redness index and release of azadirachtin from the microencapsulated oil, resulted in up to a 15 day shelf life for this fruit. This postharvest procedure has the potential to increase commercial exploitation of fresh pitaya, owing to its good taste and high content of antioxidants.

Radiosterilized pig skin (RPS) has been used as a dressing for burns since the 1980s. Its similarity to human skin in terms of the extracellular matrix (ECM) allows the attachment of mesenchymal stem cells, making it ideal as a scaffold to create cellularized constructs. The use of silver nanoparticles (AgNPs) has been proven to be an appropriate alternative to the use of antibiotics and a potential solution against multidrug-resistant bacteria. RPS can be impregnated with AgNPs to develop nanomaterials capable of preventing wound infections. The main goal of this study was to assess the use of RPS as a scaffold for autologous fibroblasts (Fb), keratinocytes (Kc), and mesenchymal stem cells (MSC) in the treatment of second-degree burns (SDB). Additionally, independent RPS samples were impregnated with AgNPs to enhance their properties and further develop an antibacterial dressing that was initially tested using a burn mouse model. This protocol was approved by the Research and Ethics Committee of the INRLGII (INR 20/19 AC). Transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis of the synthesized AgNPs showed an average size of 10 nm and rounded morphology. Minimum inhibitory concentrations (MIC) and Kirby–Bauer assays indicated that AgNPs (in solution at a concentration of 125 ppm) exhibit antimicrobial activity against the planktonic form of S. aureus isolated from burned patients; moreover, a log reduction of 1.74 ± 0.24 was achieved against biofilm formation. The nanomaterial developed with RPS impregnated with AgNPs solution at 125 ppm (RPS-AgNPs125) facilitated wound healing in a burn mouse model and enhanced extracellular matrix (ECM) deposition, as analyzed by Masson’s staining in histological samples. No silver was detected by energy-dispersive X-ray spectroscopy (EDS) in the skin, and neither by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) in different organs of the mouse burn model. Calcein/ethidium homodimer (EthD-1), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), and scanning electron microscopy (SEM) analysis demonstrated that Fb, Kc, and MSC could attach to RPS with over 95% cell viability. Kc were capable of releasing FGF at 0.5 pg above control levels, as analyzed by ELISA assays. An autologous RPS-Fb-Kc construct was implanted in a patient with SDB and compared to an autologous skin graft. The patient recovery was assessed seven days post-implantation, and the patient was followed up at one, two, and three months after the implantation, exhibiting favorable recovery compared to the gold standard, as measured by the cutometer. In conclusion, RPS effectively can be used as a scaffold for the culture of Fb, Kc, and MSC, facilitating the development of a cellularized construct that enhances wound healing in burn patients.

This review critically analyzes bioactive compounds derived from agro-industrial by-products, including polyphenols, natural pigments, dietary fiber, prebiotics, lipids, proteins, and bioactive peptides. The review examines their chemical characteristics, major agro-industrial sources, and recovery strategies, highlighting both conventional technologies and emerging green technologies, such as ultrasound-assisted extraction, supercritical fluids, and natural deep eutectic solvents (NADESs). Across compound classes, common patterns are identified, including the importance of external plant tissues as primary biological reservoirs, as well as a methodological convergence in extraction processes despite the wide chemical diversity of the molecules. Shared challenges related to compound stability, scalability, and process efficiency are also discussed. The results demonstrate that agro-industrial by-products should be understood as complex, integrated matrices rather than isolated sources of individual compounds, thereby supporting the development of unified biorefinery schemes. Unlike previous reviews focused on individual compound classes, this review integrates multiple classes of bioactive compounds, green extraction technologies, analytical characterization strategies, and industrial valorization approaches within a circular biorefinery framework. In conclusion, this review helps bridge the current fragmented understanding of waste valorization and highlights key opportunities for the sustainable development of high-value-added functional ingredients within the framework of the circular economy.

Background. Gout is an inflammatory disease caused by the deposition of monosodium urate (MSU) crystals, leading to reactive oxygen species (ROS) production and activation of the NLRP3 inflammasome with subsequent IL-1β release. Poly-gallic acid (PGAL), enzymatically synthesized polymer, has demonstrated antioxidant and anti-inflammatory properties; however, its effect on MSU-induced inflammasome activation remains unclear. Thus, this work aims to evaluate the effect of PGAL on oxidative stress and inflammatory responses induced by MSU crystals in THP-1-derived macrophages. Methods. Macrophages were pretreated with PGAL and stimulated with MSU crystals. Cell viability, apoptosis, phagocytosis, ROS and NO production, soluble urate levels, and NLRP3 and IL-1β expression were evaluated. Molecular docking and binding free energy calculations were performed to characterize PGAL–MSU interactions. Results. PGAL significantly reduced ROS and NO production, and apoptosis. PGAL treatment also decreased MSU crystal phagocytosis and significantly reduced NLRP3 and IL-1β. Computational analysis revealed that PGAL interacts with MSU crystals predominantly through electrostatic interactions, including Na⁺ coordination and hydrogen bonding. Conclusions. PGAL attenuates MSU-induced oxidative stress and NLRP3/IL-1β activation, possibly by interfering with crystal internalization. These findings suggest a mechanism based on modulation of crystal–cell interactions and downstream inflammation responses.