Chitosan biological macromolecule is a versatile polymer; chemical modification has been carried out that lead to the formation of chitosan grafted polymers composites (Chito-g-PC). We proposed synthesis of six various Chito-g-PC as sorbents for toxic dyes. A novel graft copolymerization method based on radical polymerization with vinyl monomer like acrylic acid, acrylamide, N-isopropylacrylamide, methacrylic acid and polyacrylonitrile were utilized in order to address the large amount of swelling at four different pH buffers solution. The effect of initiator and monomer concentration, time and temperature on % grafting and % grafting efficiency were performed. Comparative characterization of Chito and Chito-g-PC were evaluated by SEM, XRD and FTIR, as well as solubility characteristics of the composites were determined by various pH buffer solution. Cationic toxic dyes Malachite green (MG) and Methylene blue (MB) were selected as the sorbet, and Chito-g-PC were used as biosorbents. Thermodynamic analysis showed that the sorption process was spontaneous and endothermic with an increased randomness. The sorption experiments were realized with six different Chito-g-PC for MG and MB at various pH.

In this study, we focus on the biomimetic development of small molecules and their biological sensing with DNA. The binding of herring sperm deoxyribonucleic acid (hs-DNA) with naturally occurring bioactive small molecule α-amyrin acetate (α-AA), a biomimetic – isolated from the leaves of Ficus (F.) arnottiana is investigated. Collective information from various imaging, spectroscopic and biophysical experiments provides evidence that α-AA is a minor groove sensor of hs-DNA and preferentially binds to the A–T-rich regions. Interactions of different concentrations of small molecule α-AA with hsDNA were evaluated via various analytical techniques such as UV-Vis, circular dichroism (CD) and fluorescence emission spectroscopy. Fluorescence emission spectroscopy results suggest that α-AA decreases the emission level of hsDNA. DNA minor groove sensor Hoechst 33258 and intercalative sensor EB, melting transition analysis (T_M) and viscosity analysis clarified that α-AA binds to hs-DNA via a groove site. Biophysical chemistry and molecular docking studies show that hydrophobic interactions play a major role in this binding. The present research deals with a natural product biosynthesis-linked chemical–biology interface sensor as a biological probe for α-AA: hs-DNA.

Thermosetting materials with differing properties bond without adhesives via dynamic covalent exchange forming interfacial zone. This enables hydrophobic polymers to bond polar materials and fabricate layered composites with distinct failure modes.

We developed a cost-effective and eco-friendly click biosynthesis of small molecule quercetin–gold quantum dots (QRT–AuQDs) involving quick conjugation using an ultrasonication method at ambient temperature by utilizing QRT and gold ions in the proportion of 0.1 : 1 (molar ratio). A comparatively very short amount of time (60 seconds) was required as compared to conventional procedures. The present biomimetics research relates to the isolation of bioactive QRT by the circularly spread silica gel layer technique (CSSGLT) and characterization (UV-Vis, FTIR, NMR and DSC analysis). Characterization of the synthesized QRT–AuQDs conjugated complex was carried out by UV-Vis, HR-TEM, DLS, zeta potential and X-ray diffraction. The main objective of the present work was to study the comparative anticancer activity of QRT and QRT–AuQDs on human lung cancer HOP-62 and leukemia K-562 cell lines. The results suggested that QRT–AuQDs showed potential for applications in anticancer treatment and were found to be a more cytotoxic agent in comparison to QRT, causing > 50% inhibition of cancer cells at the concentration < 10⁻⁷ M. Hence, small molecule conjugated QRT–AuQDs can be used as a promising material for biomedical, bioengineering and anti-infectives applications.

This study examines the intrinsic optical enhancements of carbon fiber-reinforced polymers (CFRPs) achieved through the integration of magnesium oxide (MgO) nanoparticles, as well as Mg/MgO and titanium dioxide (TiO₂) thin films onto carbon fibers. Integration was performed by quasi-continuous electrophoretic deposition (EPD) and physical vapor deposition (PVD), respectively. Employing a customized electrophoretic cell, EPD facilitated uniform MgO nanoparticle deposition onto unsized carbon fibers, ensuring stable nanoparticle dispersion and precise fiber coating. As a result, the fibers exhibited increased ultraviolet (UV) reflectance, largely attributed to the optical properties of the protective MgO layer. In parallel, PVD enabled the deposition of Mg/MgO and TiO₂ thin films with tailored thicknesses, providing precise control over key optical parameters such as reflectivity and interference effects. Mg/MgO coatings demonstrated high UV reflectivity, while TiO₂ layers, with their varying refractive indices, generated vibrant colors in the visible (Vis) range through thickness-dependent light interference. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) assessed the quality, thickness, and uniformity of these thin films, and UV/Vis spectroscopy confirmed the influence of deposition parameters on the resulting optical performance. Post-lamination analyses revealed that both EPD and PVD modifications significantly enhanced UV reflectivity and allowed for customizable color effects. This dual strategy underscores the potential of combining EPD and PVD to develop advanced CFRPs with superior UV resistance, decorative optical features, and improved environmental stability.