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In this study, zinc oxide nanoparticles (ZnO‐NPs) are synthesized and combined with chitosan (Cs) to create Cs/ZnO‐NPs nanomicelles, aiming to investigate their potential as a novel cancer treatment. The ZnO‐NPs are produced through a sintering process at temperatures ranging from 300 to 700 °C. The most effective nanoparticles are obtained at 600 °C, as determined by X‐ray diffraction (XRD) and Fourier‐transform infrared spectroscopy (FTIR) analyses, which confirmed their crystallinity and purity. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are employed to characterize the size and shape of the nanoparticles, revealing predominantly spherical and hexagonal structures with stable dimensions. The cytotoxic effects of the Cs/ZnO‐NPs are evaluated against various cancer cell types. The results show that at a concentration of 125 µg mL−1, the Cs/ZnO‐NPs demonstrate significantly higher cancer cell toxicity compared to ZnO‐NPs alone, while remaining non‐toxic to normal cells. This indicates that Cs/ZnO‐NPs have a superior ability to selectively target cancer cells. These findings suggest that Cs/ZnO‐NPs nanomicelles hold promise as an effective and safe nanotherapeutic approach in the realm of cancer treatment, meriting further exploration for clinical applications. [ABSTRACT FROM AUTHOR]

This study aimed to synthesize dual‐crosslinked chitosan‐alginate nanocomposites (Cs‐Alg/IO NCs) using green‐synthesized iron oxide nanoparticles (IO, Fe3O4 NPs) for drug delivery application. The NCs, formed via ionotropic gelation with sodium tripolyphosphate (TPP) and calcium chloride (CaCl2) as crosslinking agents for Cs and Alg, respectively, and further characterized for physiochemical properties. The presence of Fe3O4 NPs and 5‐Fluorouracil (5FU) increased hydrodynamic size (153.12 ± 0.57 to 207.64 ± 3.59 nm). Morphological studies revealed NC agglomeration within nanoscales. 5FU‐loaded Cs‐Alg/IO NCs (Cs‐Alg/IO 5FU NCs) exhibited superparamagnetic behavior and sustained drug release under various pH conditions. Cytotoxicity assays on colon cancer cells (HCT116 and HT‐29) and normal colon cells (CCD‐112) indicated higher cancer cell selectivity (selectivity index, SI = 1.91) in 2D models. Elevated IC50 values in 3D models were linked to lower drug loading capacity (LC) and encapsulation efficiency (EE). Overall, the study highlights the potential of dual‐crosslinked biopolymer NCs with green‐synthesized Fe3O4 NPs for developing an anticancer drug delivery system in colorectal cancer treatment. Highlights: Synthesis of 5FU‐loaded dual crosslinked Cs‐Alg/IO NCs and Cs‐Alg IPN.Physicochemical characterization of cross‐linked magnetic nanocarriers.Investigation of sustained drug release using superparamagnetic nanocarriers.Evaluation of selective cytotoxicity for Cs‐Alg/IO 5FU NCs. [ABSTRACT FROM AUTHOR]

Copper nanoparticles (Cu‐NPs) have garnered substantial interest in the field of nanotechnology due to their exceptional physical and chemical properties and cost‐effectiveness. However, challenges such as particle aggregation and rapid copper oxidation affect nanoscale production. This study systematically investigates the synthesis of colloidal Cu‐NPs using chitosan (Cts) as a stabilizer and reducing agent in the arc discharge system, comparing it to distilled water as a medium. Confirmation of the purity, size, and morphology of the Cu‐NPs is achieved through various physicochemical characterization methods. X‐ray diffraction patterns confirm the synthesis of highly pure face‐centered cubic (fcc) crystal Cu‐NPs. UV–vis analysis reveals absorption peaks at 572–585 nm, indicating pure copper. Fourier‐transform infrared spectroscopy shows peaks at 638 and 597 cm−1, corresponding to Cu─Cts bonds. Transmission electron microscopy images depict spherical nanoparticles ranging from 15 to 45 nm, with smaller sizes at higher Cts concentrations. The catalytic activity of Cu‐NPs in the degradation of 4‐nitrophenol to 4‐aminophenol is assessed, with Cu‐NPs synthesized in distilled water demonstrating superior catalytic properties compared to 0.10 wt.% Cts. This study highlights the efficacy of the arc discharge method in producing pure, uniformly sized Cu‐NPs with potential applications in catalysis. [ABSTRACT FROM AUTHOR]

This study presents a green synthesis approach for the fabrication of zinc oxide-silver nanoparticles (ZnO-Ag-NPs) using Punica granatum fruit peels extract as a natural reducing and stabilizing agent. This eco-friendly method offers a sustainable alternative to conventional methods that often employ toxic or hazardous chemicals. Antibacterial and anti-cancer activities of the green synthesized nanoparticles were then assessed in vitro. X-ray diffraction confirmed the production of ZnO-Ag-NPs with increasing crystallinity in higher pH values. The ZnO-Ag-NPs were found to be agglomerated with spherical AgNPs. Fourier Transform Infrared (FTIR) spectra revealed a broad band in ZnOAg-NPs ranging from 400-1 to 530 cm-1 with reduced intensity as compared to ZnO-NPs, indicating the formation of Ag-NPs on the surface of ZnO-NPs. The synthesized ZnO-Ag-NPs exhibited potent antibacterial activity against a broad spectrum of bacterial strains, particularly Gram-positive bacteria, with superior inhibition activity compared to ZnO-NPs. Moreover, ZnO-Ag-NPs showed a dosedependent anti-proliferative effect on colorectal-, lung-, and cervical cancer cells. ZnO-Ag-NPs showed significantly greater efficacy in inhibiting cancer cell growth at a lower concentration of 31.25 μg/mL, compared to ZnO-NPs which required over 500 μg/mL, possibly due to the presence of silver nanoparticles (Ag-NPs). The results obtained from this study demonstrate the potential of green synthesis approaches in the fabrication of therapeutic nanomaterials for cancer treatment, as well as other biomedical applications. [ABSTRACT FROM AUTHOR]

Broiler meat can provide an appropriate environment for the microbial intensification, resulting in the lipid and protein oxidation and physico-chemical degradation. The utilisation of the anti-oxidants prevents meat degradation and human health challenges by preventing meat physico-chemical characteristics. Pullulan active packaging incorporated with green silver nanoparticles, as anti-oxidants, has not been reported in broiler meat preservation. Therefore, the impact of pullulan active packaging, incorporated with curcumin and pullulan mediated silver nanoparticles (C-AgNPs, P-AgNPs) on broiler meat was determined in the current study for 14 days of refrigerated storage at 4 ± 1 °C. A total of 120 broiler birds were reared for clean meat production and divided into 4 treatment groups (PF-CTRL, PF-C-AgNPs, PF-P-AgNPs, PF-M-AgNPs). Pullulan active packaging maintained meat textural attributes and pigment stability and breast muscle pH (6.11). Broiler meat treated with pullulan active packaging incorporated with curcumin arbitrated AgNPs (PF-C-AgNPs) indicated significantly higher oxidative stability (p =.000), water holding capacity (p =.002), expressible fluids (p =.000), and shear force values (p =.000) along with significantly lower cooking losses (p =.000), pH (p =.000), and shear force energy (p =.000) as compared to the control (CTRL) and other treatment groups. Broiler breast meat samples treated with pullulan active packaging expressed a "lighter" appearance (53.61 ± 3.64) during the refrigerated storage of 14 days. Moreover, significant differences were recorded in the oxidative stability/MDA (mg/kg) concentrations amongst the controlled and the treated groups on day 7th (p =.000) and day 14th (p =.000) of refrigerated storage. The current study confirms that the pullulan active packaging, incorporated with curcumin arbitrated silver nanoparticles (PF-C-AgNPs) followed by pullulan active meat packaging incorporated with pullulan mediated silver nanoparticles (PF-P-AgNPs) maintained the textural and physico-chemical meat attributes along with minimal oxidative rancidity in 14 days of storage. It is concluded that PF-C-AgNPs and PF-P-AgNPs can be a safer antioxidant alternate to preserve broiler meat quality and oxidative stability with a prolonged shelf life. Pullulan active meat packaging, incorporated with C-AgNPs and P-AgNPs, should be considered as green and bio-degradable substitution of the hazardous synthetic antioxidant packaging. Pullulan active meat packaging (PF-C-AgNPs, PF-P-AgNPs) is able to maintain the textural characteristics, compositional integrity, and physico-chemical attributes of broiler meat. Broiler meat treated with PF-C-AgNPs and PF-P-AgNPs reflects better oxidative stability with prolonged shelf life. [ABSTRACT FROM AUTHOR]

Functional polymeric biomaterials (FPBMs) with bioactive characteristics obtained by radiation-induced graft copolymerisation (RIGC) have been subjected to intensive research and developed into many commercial products. Various studies have reported the development of a variety of radiation-grafted FPBMs. However, no reports dealing with the quantitative evaluations of these studies from a global bibliographic perspective have been published. Such bibliographic analysis can provide information to overcome the limitations of the databases and identify the main research trends, together with challenges and future directions. This review aims to provide an unprecedented bibliometric analysis of the published literature on the use of RIGC for the preparation of FPBMs and their applications in medical, biomedical, biotechnological, and health care fields. A total of 235 publications obtained from the Web of Science (WoS) in the period of 1985–2021 were retrieved, screened, and evaluated. The records were used to manifest the contributions to each field and underline not only the top authors, journals, citations, years of publication, and countries but also to highlight the core research topics and the hubs for research excellence on these materials. The obtained data overviews are likely to provide guides to early-career scientists and their research institutions and promote the development of new, timely needed radiation-grafted FPBMs, in addition to extending their applications. [ABSTRACT FROM AUTHOR]

The main objective of the present work is to investigate the thermal degradation behaviour of the non-catalytic and catalytic co-pyrolysis of empty fruit bunch (EFB) and high-density polyethylene (HDPE) over commercial hydrogen exchanged zeolite socony mobil five (HZSM-5) and rice husk ash (RHA) catalysts via thermogravimetric analyser (TGA). RHA catalysts were produced using the solvent-free method by converting RHA into HZSM-5. XRD characterization was conducted for the synthesized catalysts and RHA catalyst showed less amount of peaks compared to commercial HZSM-5. Non-catalytic and catalytic co-pyrolysis of EFB and HDPE over commercial HZSM-5 and RHA catalysts were conducted using TGA. A fixed EFB-toHDPE mass ratio of 1:1 and a fixed catalyst-to-feedstock mass ratio of 1:1 were used for the TGA experiments. The sample was heated up under pyrolysis conditions at a heating rate of 20 °C/min until 700 °C. The thermal degradation behaviour of EFB and HDPE did not change significantly when RHA catalysts were used, based on the TG curves. Volatilization of matter was maximum between temperatures 240 °C and 500 °C (Phase II) for all cases of the pyrolysis process, where the highest volatilized matter of 93.2 wt% was produced from the catalytic process over commercial HZSM-5, followed by the catalytic process over RHA catalysts with 92.3 wt% of volatilized matter and non-catalytic process with 83.0 wt% of volatilized matter. When using catalysts, 0.44 wt% of solid residual was left when commercial HZSM-5 was used while 0.38 wt% of solid residual was left when RHA catalyst was used. [ABSTRACT FROM AUTHOR]

The main objective of the current work is to investigate the influence of waste chicken eggshell (WCE) as an alternative source of calcium oxide (CaO) on Hydrogen exchanged Zeolite Socony Mobil-5 catalyst (HZSM-5). WCE as promoter was loaded at 1wt.% on HZSM-5 catalyst which act as support via incipient wetness impregnation method. The HZSM-5, commercial CaO, and WCE were individually prepared for comparison with WCE/HZSM-5. Synthesized catalysts were characterized via X-Ray Diffraction to analyse the phase purity, Field Emission Scanning Electron Microscopy to analyse the surface morphology, and Brunauer-Emmett-Teller to analyse the surface area and pore size. The addition of WCE on HZSM-5 has significantly affected the framework structure of HZSM-5 where the crystallinity percentage and average crystal size of HZSM-5 drastically dropped to 44.97 % and 45.00 nm. The original cubic-like structure in HZSM-5 has significantly altered into a netlike structure after the impregnation of WCE. A similar effect of alteration was observed on BET surface area dropped from 365.81 m2 /g (HZSM-5) to 292.14 m2 /g (WCE/HZSM-5). Interestingly, the pore diameter of WCE/HZSM-5, WCE, and HZSM-5 catalysts was similar at 3.88 nm, 3.87 nm, and 3.87 nm respectively. WCE and commercial CaO almost share similar textural properties. Hence, the addition of WCE as an alternative source of calcium oxide into HZSM-5 can provide a high catalytic reaction and stable surface in catalytic cracking of heavy hydrocarbons into small hydrocarbons with longer catalyst lifetimes. [ABSTRACT FROM AUTHOR]

Nanoemulsions (NEs) as multi-compartmentalized systems are extensively considered as versatile drug delivery systems, due to their multifunctional and tuneable physicochemical properties. Here, water-in-oil-in-water (WOW) NEs were formulated using Juglans regia -based Fe 3 O 4 /Au-core-shell nanoparticles to encapsulate 5-Fluorouracil (5-FU) for potential colorectal cancer treatment. Response surface methodology, FTIR, TGA, TEM, DLS, VSM, UV-vis spectroscopy, and viscosity measurements were used to characterize the fabricated samples. The analysis confirmed the successful synthesis of Au, Fe 3 O 4 , and Fe 3 O 4 /Au core-shell nanoparticles with the Juglans regia (J. regia) extract as a green stabilizer and also reducing agent. The NE displayed a spherical-shape and TEM size of~30 nm. It also exhibited good colloidal stability and multifunctional features related to its components. TGA data indicated that 5-FU increased thermal stability after its loading into the nanoemulsion as a drug carrier. 5-FU release from the NE carrier presented a time-delayed behavior and higher release dosage in media at pH 4 compared to pH 7 within 48 h. When tested against colorectal-derived cell lines, 0.78 µg/mL of 5-FU-loaded Fe 3 O 4 /Au core-shell NEs showed potent anticancer activity against HCT116 cancerous cells, while exhibiting low toxicity towards CCD112 normal cells. In conclusion, the synthesized 5-FU-loaded NEs can be potently used as an anticancer drug carrier model, owing to its nano-scale size and other functionalities, which should be further studied. [ABSTRACT FROM AUTHOR]

The production of pure silver nanoparticles (Ag-NPs) with unique properties remains a challenge even today. In the present study, the synthesis of silver nanoparticles (Ag-NPs) from natural pullulan (PL) was carried out using a radiation-induced method. It is known that pullulan is regarded as a microbial polysaccharide, which renders it suitable to act as a reducing and stabilizing agent during the production of Ag-NPs. Pullulan-assisted synthesis under gamma irradiation was successfully developed to obtain Ag-NPs, which was characterized by UV-Vis, XRD, TEM, and Zeta potential analysis. Pullulan was used as a stabilizer and template for the growth of silver nanoparticles, while gamma radiation was modified to be selective to reduce silver ions. The formation of Ag-NPs was confirmed using UV–Vis spectra by showing a surface plasmon resonance (SPR) band in the region of 410–420 nm. As observed by TEM images, it can be said that by increasing the radiation dose, the particle size decreases, resulting in a mean diameter of Ag-NPs ranging from 40.97 to 3.98 nm. The XRD analysis confirmed that silver metal structures with a face-centered cubic (FCC) crystal were present, while TEM images showed a spherical shape with smooth edges. XRD also demonstrated that increasing the dose of gamma radiation increases the crystallinity at a high purity of Ag-NPs. As examined by zeta potential, the synthesized Ag-NP/PL was negatively charged with high stability. Ag-NP/PL was then analysed for antimicrobial activity against Staphylococcus aureus, and it was found that it had high antibacterial activity. It is found that the adoption of radiation doses results in a stable and green reduction process for silver nanoparticles. [ABSTRACT FROM AUTHOR]

The interest in developing antimicrobial surfaces is currently surging with the rise in global infectious disease events. Radiation-induced graft copolymerization (RIGC) is a powerful technique enabling permanent tunable and desired surface modifications imparting antimicrobial properties to polymer substrates to prevent disease transmission and provide safer biomaterials and healthcare products. This review aims to provide a broader perspective of the progress taking place in strategies for designing various antimicrobial polymeric surfaces using RIGC methods and their applications in medical devices, healthcare, textile, tissue engineering and food packing. Particularly, the use of UV, plasma, electron beam (EB) and γ-rays for biocides covalent immobilization to various polymers surfaces including nonwoven fabrics, films, nanofibers, nanocomposites, catheters, sutures, wound dressing patches and contact lenses is reviewed. The different strategies to enhance the grafted antimicrobial properties are discussed with an emphasis on the emerging approach of in-situ formation of metal nanoparticles (NPs) in radiation grafted substrates. The current applications of the polymers with antimicrobial surfaces are discussed together with their future research directions. It is expected that this review would attract attention of researchers and scientists to realize the merits of RIGC in developing timely, necessary antimicrobial materials to mitigate the fast-growing microbial activities and promote hygienic lifestyles. [ABSTRACT FROM AUTHOR]

The present study details a more environmentally friendly method for synthesizing iron oxide nanoparticles (Fe3O4‐NPs) utilizing Hibiscus sabdariffa (H. sabdariffa) leaf extract. The produced H. sabdariffa/Fe3O4‐NPs underwent characterization through VSM, XRD, FESEM‐EDX, TEM and FTIR analyses. The FESEM and TEM images revealed that the H. sabdariffa/Fe3O4‐NPs had a narrow distribution and an average particle size of 5±2 nm. Catalytic degradation studies of the synthesized Fe3O4‐NPs exhibited efficient reduction of methyl orange (MO) dye. The degradation of MO catalysed by H. sabdariffa/Fe3O4‐NPs follow the pseudo‐first order kinetics, with a rate constant of 0.0328 s−1 (R2=0.9866). Moreover, in electrochemical sensing studies, the anodic peak current of nitrite (NO2−) for H. sabdariffa/Fe3O4‐NPs/GCE showed a linear relationship with its concentration within the range of 0.5–7.5 mM, achieving a detection limit of 0.29 μM. These findings demonstrate that the modified electrode with Fe3O4‐NPs synthesized using H. sabdariffa leaf extract serve as a novel electrochemical sensor for determining NO2− with high sensitivity and reproducibility. [ABSTRACT FROM AUTHOR]