This study demonstrated, for the first time, the successful formation of porous paramylon esters, which were made from euglenoid polysaccharide known as paramylon and short-chain fatty acids, through supercritical CO₂ processing. By maintaining a constant ester functional group attached to the paramylon and varying its proportion, distinct porous structures were selectively produced. Solubility parameter estimations indicated that changes in esterification had no significant effect on the solubility of the paramylon esters used in the experiment. Thus, these structural differences are likely attributed to variations in the viscoelastic properties of paramylon esters under supercritical CO₂ conditions. Furthermore, thermal conductivity measurements revealed reductions of up to 20%. Intriguingly, substantial decreases in thermal conductivity were observed even at low foaming ratios, achieved through precise control of the porous structure.

Three-dimensional (3D) bioprinting is a technique currently used for creating tissue engineering scaffolds, using bioinks as the building blocks. These bioinks are composed of biomaterials that provide structural integrity and are synthesized from organic polymers to enhance biocompatibility with the printed constructs. In this study, a series of eleven chitosan-based bioinks were synthesized using the sol-gel technique, employing chitosan of low and medium molecular weight. Three bioink formulations were selected based on their viscosity characteristics and further enriched with gelatin and hydroxyapatite (HA) to enhance their mechanical properties. Characterization tests included Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and rheological assessments. Viscoelastic materials were obtained, and an experimental model was developed to optimize printing parameters, focusing on pressure and printing speed. Our findings indicate that a bioink formulation comprising a blend of medium and high molecular weight chitosan, supplemented with gelatin and hydroxyapatite, was found to be a promising approach for fabricating scaffolds for bone tissue repair.

Biodegradable biopolymers like polyhydroxybutyrate (PHB) hold promise for sustainable packaging, but their inherent degradability reduces material stability. Synthetic stabilizers, though effective, raise environmental and potential toxicity concerns. This study explores a multifunctional natural anti-aging agent: a hemp extract rich in cannabidiol (CBD) and cannabichromene (CBC). PHB composites with varying hemp extract concentrations were prepared and subjected to thermooxidative and weathering aging. Characterization employed FTIR-ATR, carbonyl index, and spectrophotometry. Static mechanical properties, DSC, and surface free energy (SFE) were also assessed. Notably, the hemp extract exhibited stability under ambient conditions but showed migration with time and aging. The results suggest a plasticizing effect on PHB and highlight the contrasting roles of the extract: inhibiting thermooxidative aging while potentially accelerating aging under atmospheric conditions. This opens avenues for tailoring material durability, further evaluated by life cycle analysis (LCA). This work represents one of the first investigations into hemp extract as an anti-aging agent for eco-friendly polymers, expanding the knowledge base of natural multifunctional additives.

The widespread use of cellulose nanofiber (CNF)-based aerogels is hindered by their limited flame retardancy and mechanical properties. This study addresses these challenges by developing cellulose nanofiber/sodium alginate/fly ash (CNF/SA/FA) aerogel through a one-pot method, utilizing industrial waste fly ash (FA) as a reinforcing material. Various characterization and analytical techniques were employed to evaluate the properties of the CNF/SA/FA aerogel. The findings have revealed that resulting aerogel exhibited excellent thermal insulation performance, with a thermal conductivity of 0.485 W/(m·K), along with an impressive compressive strength of 88.4 kPa and favorable shape processability. Vertical combustion tests demonstrated a V-0 rating, indicating superior flame retardancy, and the aerogel achieved a remarkable 79.16% residual carbon, confirming their effective heat shielding capabilities. Notably, the incorporation of FA significantly enhanced both the thermal and mechanical properties of the composite aerogel, presenting a sustainable and effective solution to optimizing the properties of aerogel for thermal insulation.

Polymer-based hydrogels are hydrophilic polymer networks with a remarkable capacity to absorb substantial amounts of water and biological fluids, rendering them highly attractive for drug delivery applications. The COVID-19 pandemic has acted as a catalyst for research and innovation in the realm of polymer-based hydrogels for drug delivery, with a particular emphasis on antiviral therapeutics, vaccines, diagnostics, and precision delivery to the respiratory system. The distinctive attributes of hydrogels, such as their biocompatibility, customizable drug release profiles, and ease of functionalization, establish them as versatile platforms for the development of advanced drug delivery systems to combat not only COVID-19 but also a spectrum of other infectious diseases. This study is dedicated to scruti-nizing and evaluating the characteristics of polymer-based hydrogels employed in drug delivery for the treatment of diseases associated with the SARS-CoV-2 virus. Furthermore, the investigation introduces a novel classification system for polymer-based hydrogels deployed in drug delivery for SARS-CoV-2-related diseases. Additionally, the paper provides an up-to-date evaluation of the latest developed hydrogels utilized in drug delivery for the treatment of dis-eases linked to the SARS-CoV-2 virus, based on research conducted through the recent months of 2023.