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This analysis theoretically investigates the transport phenomena of mixed convection flows in an enclosure of rectangular geometry saturated with a permeable medium filled with an electrically conducting nanofluid. An inclined magnetic field is taken into consideration. Buongiorno's model is utilized to characterize the nanoliquid. The enclosure has adiabatic walls and hot slits. A uniform cold temperature is maintained at the enclosure's lower and upper walls. The enclosure's vertical walls are thermally insulated with hot slits at the center of the walls. This kind of analysis on mixed convective, electrically conducting nanofluid flows in enclosures finds applications in smart nanomaterial processing systems and hybrid electromagnetic nanoliquid fuel cells. The Marker-And-Cell (MAC) method is utilized to solve the transformed nondimension system of governing equations subject to the fitted boundary conditions. The effects of key physical parameters on streamlines, isotherms, iso-concentration contour plots and the heat transmission rate are examined. The simulations demonstrate that the Richardson number has a predominant impact on the thermo-solutal features of nanofluid flow in the rectangular enclosure. Variations in magnetic field and buoyancy ratio parameters exert a notable influence on the iso-concentrations and isotherms. An increase in the Darcy number values exhibits a tendency to magnify the local heat transfer rate. Higher Grashof number values reduce the local Nusselt number profiles. The effect of porous parameter is significant in the streamlines, isotherms and iso-concentrations. Thus, the porous medium can significantly control the transport phenomena in the enclosure. The concentration, temperature and velocity contours are strongly modified by the variations in the Grashof number. [ABSTRACT FROM AUTHOR]

The brittleness and limited plastic deformation of ceramics restrict their applications. In this work, the effects of pristine (CNT P), functionalized (CNT OH , CNT COOH) and silanized MWCNTs on the mechanical properties of Silicon Carbide obtained by pyrolyzing polycarbosilane SMP-10 were studied. Functionalization with 3-glycidoxypropyltrimethoxy was analyzed through dispersion stability, zeta potential, and EDS analyses, revealing increased silicon content and colloidal stability in silanized MWCNTs. However, silanized MWCNTs led to reduced mechanical properties in composites, while untreated MWCNTs (CNT P , CNT OH , CNT COOH), showed a substantial increase in modulus by 74.2 %, 86.9 %, and 30.5 %, respectively. The observed enhancement in mechanical properties exceeded the outcomes predicted by the rule of mixtures, suggesting notable morphological changes induced by MWCNTs. Potential underlying factors including toughening mechanisms and changes in porosity were evaluated and discussed in depth. Composites with untreated MWCNTs showed nearly a two-fold increase in fracture toughness. This work shows a streamlined approach for the development of ceramic nanocomposites (CNCs), achieving significant improvement in mechanical properties through pyrolysis, surpassing traditional methods reliant on densification processes. These findings demonstrate the substantial potential of CNCs, enhancing their suitability for advanced engineering applications. [ABSTRACT FROM AUTHOR]

The present work reports a synthesis of octahedron (A55NO) and cube-shaped (A55NC) Mn 0.5 Zn 0.5 Fe 2 O 4 ferrite nanoparticle dispersion in distilled water. The crystal structure analyzed using powder X-ray diffraction (XRD) shows the crystallite sizes of 17.7 ± 0.4 nm and 11.9 ± 1.0 nm, respectively, for the A55NO and A55NC particles. The morphology as seen from transmission electron microscopy (TEM) confirms 17.8 ± 0.3 nm (σ = 0.27) and 8.7 ± 0.3 nm (σ = 0.33) edge lengths, respectively, for octahedron and cube-shaped particles. The thermogravimetric analyzer (TGA) and Fourier transform infrared (FTIR) spectroscopy are used to confirm the chemical binding of the surfactant with a sharp transition at 208.67 °C and 218.32 °C, respectively, for octahedron and cube-shaped particles, indicating the removal of the surfactant due to its decomposition from the particle surface. Both the particles are highly magnetic and have 75.32 Am2/kg and 72.93 Am2/kg saturation magnetization, as revealed by their M − H loops using a vibrating sample magnetometer (VSM). The stability of the sample is confirmed using the particle size analyzer (DLS) and the Zeta potential analyzer. The induction heating capacity of the fluid was investigated using the Embrell Easy Heat model LA6310 at 330 kHz. The heating response shows that even a minimum concentration of 1 mg/mL is sufficient to achieve the hyperthermic window temperature of 42 °C for both samples, which, unlike the same composition prepared by other routes, makes it impossible to go beyond 38 °C. Moreover, octahedron particle dispersion can reach this window temperature within 10 min, whereas cube particle dispersion requires only 15 min. The findings of this study hold significant practical value since it confirms that Mn 0.5 Zn 0.5 Fe 2 O 4 composition with tuneable shape has the potential to work as a temperature-controlled magnetic switch for magnetic fluid hyperthermia under the defined safety limit with the minimum concentration. [ABSTRACT FROM AUTHOR]

The zinc doped calcium phosphate biomaterials have recently attracted much attention. In this study, we have investigated the bioactivity, cytotoxicity and antibacterial activity of zinc doped calcium phosphate-sulfate hydroxyapatites Ca 9-x Zn x Na(PO 4) 5 (SO 4)(OH) 2 (x = 0, 0.2, 0.5). The samples have been synthesized by the solid-state reaction at high temperature and then have been characterized using X-ray diffraction, Infrared spectroscopy and Raman scattering spectroscopy. The surface analysis was conducted by scanning electron microscopy (SEM) in combination with energy-dispersive spectroscopy (EDX) and Zeta-potential measurements. The bioactivity investigation involved immersing the samples in a simulated body fluid (SBF), providing valuable insights into the samples capability to stimulate the formation of an apatite layer similar to that found in bones. The antibacterial activity of the materials was studied using pathogenic bacteria. The assessment of sample cytotoxicity was involved using artemia salina as the experimental model. X-ray diffraction patterns reveal that the samples crystallize in the hexagonal system with the P 6 3 / m space group. The x = 0.2 material exhibited the best crystallinity and the highest negative Zeta potential, making it the most bioactive sample when immersed in simulated body fluid (SBF). SEM analysis confirmed that this sample effectively promotes the formation of a new apatite layer, highlighting its promising potential for biomedical applications. The results of the study highlight the significantly beneficial effect of doped hydroxyapatite (x = 0.2) on the biological properties, compared to the other samples analyzed in this study, thus underscoring the strong potential of this material for promising applications in the fields of bioengineering and tissue regeneration. [ABSTRACT FROM AUTHOR]

Functionalized nanomaterials with surface-active groups have garnered significant research interest due to their wide-ranging applications, particularly in water treatment for removing various contaminants. This study focuses on developing a novel, multi-functional nanobiosorbent by synthesizing nanosized biochar from artichoke leaves (NBAL) and molybdic acid (MA). The resulting nanobiosorbent, MA@NBAL, is produced through a microwave-irradiation process, offering a promising material for enhanced environmental remediation. The characteristics of assembled MA@NBAL were evaluated from SEM-EDX, XPS, TGA, FT-IR, and zeta potential detection. The size of particles ranged from 18.7 to 23.7 nm. At the same time, the EDX analysis denoted the existence of several major elements with related percentage values of carbon (52.9%), oxygen (27.6%), molybdenum (8.8%), and nitrogen (4.5%) in the assembled MA@NBAL nanobiosorbent. The effectiveness of MA@NBAL in removing Hg(II) ions was monitored via the batch study method. The optimized maximum removal capacity of Hg(II) ions onto MA@NBAL was established at pH 6.0, 30.0 min equilibrium time, and 20 mg of nanobiosorbent, providing 1444.25 mg/g with a 10.0 mmol/L concentration of Hg(II). Kinetic studies revealed that the adsorption process followed a pseudo-second-order model, with R2 values ranging from 0.993 to 0.999 for the two tested Hg(II) concentrations, indicating excellent alignment with the experimental data. This suggests that the chemisorption mechanism involves cation exchange and complex formation. Isotherm model evaluation further confirmed the adsorption mechanism, with the Freundlich model providing the best fit, yielding an R2 of 0.962. This result indicates that Hg(II) adsorption onto the surface of MA@NBAL nanobiosorbent occurs on a heterogeneous surface with multilayer formation characteristics. The results of the temperature factor and computation of the thermodynamic parameters referred to endothermic behavior via a nonspontaneous process. Finally, the valid applicability of MA@NBAL nanobiosorbent in the adsorptive recovery of 2.0 and 5.0 µg/mL Hg(II) from contaminated real aquatic matrices was explored in this study, providing 91.2–98.6% removal efficiency. [ABSTRACT FROM AUTHOR]

At present, animal bone glue has been widely used in industry, but there are no relevant research reports on its application in the petroleum industry. In this paper, the rheological properties, inhibition, filtration, and temperature resistance performance of modified bone glue (Mbg) were evaluated in water-based drilling fluids, and the results showed that Mbg can significantly affect the performance of water-based muds with minimal dosage, and temperature resistance of Mbg could reach up to 130 °C. The inhibition mechanism of Mbg in drilling fluids was investigated by infrared spectroscopy (FT-IR), X-ray diffraction (XRD), zeta potential, thermogravimetric analysis (TGA), and scanning electron microscope (SEM). Results revealed that when 2% Mbg was added, a three-dimensional network structure was formed in an aqueous solution, which reduced the water content from 4.83% to 4.23%. FT-IR analysis showed that Mbg strongly adsorbed onto clay through hydrogen bonding, which reduced the clay particles in based muds from 1.251 µm to 0.789 µm and effectively controlled the filtration loss of the drilling fluids. [ABSTRACT FROM AUTHOR]

This research targets the need for eco-friendly strategies in the synthesis of bioactive materials, addressing the importance of valorization of vegetal waste. This study focuses on developing biohybrids containing biomimetic lipid vesicles and phytosynthesized gold–silver chloride nanoparticles (AuAgCl NPs) derived from Achillea millefolium L. extract. By leveraging the natural antioxidant and antimicrobial properties of the plant, the research proposes a sustainable approach to creating materials with potential biomedical applications. The biomimetic membranes were loaded with chlorophyll a, a natural spectral marker. Three types of bioactive materials (biohybrids) were developed by varying the lipid vesicle/AuAgCl NP ratio. Optical (UV-Vis, fluorescence emission, FTIR), structural (XRD), elemental (EDX, XPS), and morphological (TEM) studies were performed to characterize the bio-developed materials. The hydrophobic/hydrophilic characteristics of the samples were investigated by measuring the water contact angle, and their size was estimated by DLS and TEM. Zeta potential measurements were used to evaluate the physical stability of phyto-developed particles. Antioxidant properties of phyto-particles were investigated through the chemiluminescence technique. The obtained biomaterials exhibited high antioxidant activity and antiproliferative activity against HT-29 and B-16 cancer cells. Therapeutic index values were calculated for each biohybrid. Additionally, the bio-prepared hybrids revealed biocidal action against Staphylococcus aureus and Enterococcus faecalis. The phyto-developed biomaterials are promising in biomedical applications, particularly as adjuvants in cancer therapy. [ABSTRACT FROM AUTHOR]

AbstractCarvacrol is a consolidated natural antimicrobial. However, its use in food is a challenge due to characteristic odour and high volatility. Nanoencapsulation has emerged to overcome these drawbacks. Aspergillus spp. represent a concern in grapes for causing rot and producing mycotoxins. This study aimed to evaluate the effect of carvacrol (unencapsulated and loaded into Eudragit® and chia nanocapsules) on the growth of Aspergillus species. Spore germination and mycelial growth of Aspergillus spp. were evaluated using the agar dilution culture method. The stability of nanocapsules during storage was monitored monthly by evaluating the particle size distribution, polydispersity index, and zeta potential. Antifungal and antitoxigenic effectiveness of nanocapsules were assessed by counting fungal colony-forming units and determining mycotoxin levels in grapes. A dose-dependent effect of carvacrol (unencapsulated and encapsulated forms) on spore germination and mycelial growth was observed. During 180 days of storage, carvacrol into Eudragit® nanocapsules preserved their nanometric dimensions, whereas chia nanocapsules maintained this characteristic for 30 days. The antifungal effectiveness of both encapsulated forms persisted for 210 days. No mycotoxin was found, even when fungal growth was not completely suppressed. Nanoencapsulated carvacrol proved to be a new promising antifungal product to ensure quality and safety in the grape production chain. [ABSTRACT FROM AUTHOR]

Carboxylate appended biochar BCKA was synthesized by a two‐step functionalization of leached rice straw biochar using ethyl 2‐bromoacetate/K2CO3/DMF and hydrolysis to furnish the modfied biochar. The modified biochar was characterized using proximate analysis, CHNS, SS CPMAS 13C NMR, FESEM, FTIR, XPS, BET, and zeta potential. Biochar BCKA was optimized for pH and dose, respectively, as 7 and 0.2 g/L for methylene blue (MB) adsorption with a contact time of 6 h at 298 K. MB removal up to 98% from 20 mg/L dye solution, using BCKA as adsorbent pH 7, 298 K. The nonlinear fit to Langmuir, Freundlich, Temkin, SIPS, and D‐R adsorption isotherm showed a good fit with correlation coefficients (R2) 0.970, 0.969, 0.988, 0.984, and 0.983, respectively, and maximum MB adsorption (qm) of 261 mg/g. Thermodynamic parameters for the adsorption of MB using BCKA were 38.72 kJ/mol (∆H°), 225.42 J/mole K (∆S°), and negative ∆G° confirming the spontaneity driven by entropy. Kinetic studies showed good nonlinear fit to pseudo‐second order (R2 0.967), intraparticle diffusion (R2 0.977), and Elovich equation (R2 0.958) with chemisorption‐based interaction between BCKA and MB. Chemisorption, particularly ion exchange on the surface of BCKA with MB, is inferred from the D‐R isotherm and kinetic analysis. Column breakthrough studies showed Thomas model fit with qt 267.09 mg/g, and efficiency >80% was retained for two cycles of MB adsorption. [ABSTRACT FROM AUTHOR]

Researchers are exploring sustainable methods for synthesizing metal oxide nanoparticles to address wastewater pollution, which poses a global threat to aquatic life and human health. The present research aims to biosynthesize recyclable Lemon peel‐extracted copper oxide nanoparticles (CuO NPs) to remove methylene blue dye via adsorption. Our approach involves a comprehensive range of techniques, such as FTIR, XRD, SEM‐EDX, Zeta potential, and UV‐VIS, to thoroughly characterize the NPs. SEM analysis confirmed that the CuO NPs, with an average size of 64.5 nm and a nearly spherical shape, exhibited a zeta potential value of – 16.34, indicating their relative stability. Optimized conditions for the 92.20% adsorption efficiency for methylene blue dye were pH at 6, contact time of 90 min, 0.06 g of adsorbent dose, 10 ppm dye conc., and Temp. 27 °C. Langmuir 1‐based maximum adsorption capacity (qm) was 617.28 mg/g for CuO NPs. Langmuir 1 and Freundlich are the most suitable isotherm models for experimental data, supporting Physi‐chemisorption and chemisorption as rate‐limiting steps in the exothermic adsorption process. A reusability study of up to three cycles proved the sustainability of the materials. [ABSTRACT FROM AUTHOR]

The article reports the synthesis of an ordered mesoporous network of heterophase TiO2 monoliths as a visible light-responsive photocatalyst using tri-block copolymers of Pluronic F108, P123 and F127 as structure-directing agents (SDAs) and temperature-controlled calcination (450–650 °C) has been carried out by direct templating-assisted hydrothermal approach. The structural/surface morphology and topographical properties of the photocatalyst are characterized using FE-SEM-EDAX, HR-TEM-SAED, p-XRD, VB-XPS, PLS, TG/DTA, UV-Vis-DRS, BET/BJH and zeta potential analysis. The undoped heterophase mesoporous TiO2 monoliths with in-built lattice/surface defects exhibit visible light photocatalytic properties, successfully dissipating Reactive Brown 10 (RB-10) dye. The influence of physicochemical parameters, such as SDAs, temperature, pH, dye concentration, catalyst dosage, photosensitizers and light intensities, are optimized for maximum photocatalytic performance at a shorter timespan. The F127-assisted mesoporous TiO2 monolith (550 °C) exhibits superior degradation kinetics (15 min) for RB-10 dye solution (20 ppm) at pH 2.0–3.0 using a photocatalyst dosage of 50 mg and 2 mM of KBrO3, irradiated with 150 W/cm2 tungsten lamp. The photocatalysts are fabricated without complicated chemical modifications and display topmost efficiency in quickly decontaminating persistent pollutants. The photoproducts from RB-10 photocatalytic degradation are investigated using HR-MS analysis. The photocatalyst can be reused efficiently for six cycles, even under extreme conditions. [ABSTRACT FROM AUTHOR]

Water-soluble fluorescent N-doped carbon quantum dots (N-CQDs) were hydrothermally prepared through a green synthesis route using castor seeds as a single precursor and a hydrothermal method. Several experimental techniques have been used to characterize synthesized N-CQDs to confirm their structure and to verify their applicability in cell imaging and pH sensing. The synthesized N-CQDs were found to have are characterized by amorphous nature with a spherical shape with an average particle size of 6.57 nm as revealed from XRD and TEM measurements. The FTIR results reveal the presence of carboxylic and hydroxyl functional groups on the surface of the CQDs, which was also confirmed by XPS analysis. The fluorescence characterization of the synthesized N-CQDs showed blue emission and excitation dependence with good photostability. It was found that the optimal excitation and emission wavelengths were (λEx = 360) and (λEm = 432) nm, respectively. The fluorescence quantum yield (QY) of about 9.6% at the optimum excitation wavelength 360 nm. Moreover, the fluorescence intensity of N-CQDs showed good linear dependence with the pH values in ranges of 3.5 − 7.5 and 8 − 12 as well as high sensitivity for slight changes of pH values. According to these results, two fluorescent pH sensors were created based on acidic and basic media. The obtained N-CQDs have zeta potential of -21.86 mV and thus have excellent stability in water. Moreover, N-CQDs derived from the castor seeds have antimicrobial activity and exhibits low cytotoxicity to WI-13 cells with IC50 = 394.4 ± 13.8 µg/mL. The results of this study demonstrated that the synthesized N-CQDs derived from castor seeds can be used as pH sensing and antimicrobial materials. On the other hand, they are also promising in applications in cell imaging, thermo-sensing and optoelectronics. [ABSTRACT FROM AUTHOR]

Telomerase enzyme prevents telomere shortening during division, having human telomerase reverse transcriptase (hTERT) as its catalytic subunit. Favipiravir (FAV), an RNA-dependent RNA polymerases inhibitor, shared structural similarity with hTERT and thus assumed to have cytotoxic effect on cancer cells, in addition to its prophylactic effect to immunocompromised cancer patients. Nanoemulsion (NE) is a potential tumor cells targeting delivery system, thereby enhancing therapeutic efficacy at the intended site, mitigating systemic toxicity, and overcoming multidrug resistance. The objective of this study is to develop a green FAV nanoemulsion (FNE) that is environmentally friendly and safe for patients, while aiming to enhance its cytotoxic effects. The study also highlights the environmental sustainability of the developed RP-HPLC method and assesses its greenness impact. The FNE formulation underwent thermodynamic stability testing and invitro characterization. Greenness was assessed using advanced selected tools like the Analytical Eco-Scale (AES), Analytical Greenness Metric for Sample Preparation (AGREEprep), and green analytical procedure index (GAPI). The cytotoxic potential of FNE was screened against MCF-7 breast cancer and Vero normal cell lines using SRB assay. Stable and ecofriendly FNE was formulated having a particle size (PS) of 25.29 ± 0.57 nm and a zeta potential of -6.79 ± 5.52 mV. The cytotoxic effect of FNE on MCF-7 cells was more potent than FAV with lower IC50 while FNE showed non-toxic effect on VERO normal cell line. Therefore, the FAV nanoemulsion formulation showed targeted cytotoxicity on MCF-7 cells while being non-toxic on normal Vero cells. [ABSTRACT FROM AUTHOR]

Innovative applications of foam are the need of time which fundamentally depends on the stability of the foam. In the present research work, the static foam behavior of the nonionic surfactant Tween-20 in the presence and absence of Titanium dioxide nanoparticles (TiO2-NPs) was investigated. The role of TiO2-NPs on foaming power based on foam height and foamability was studied at different temperatures. At 29 ± 1 0C, maximum foam height for Tween 20 (5% surfactant solution in distilled water) without and with TiO2-NPs was increased from 45.60 to 60.30 cm exhibiting 32.25% increase. In view of studying foam stability, axial dye displacement rate (ADDR) test was performed without and with nanoparticles where TiO2-NPs resist liquid drainage. TiO2 -NPs and Tween-20 form intermolecular hydrogen bonding which helps to enhance the foam stability as revealed by the density functional theory (DFT) studies. However, TiO2 -NPs have tendency to agglomerate if zeta potential value is low that severely affect the foaming power and foamability. [ABSTRACT FROM AUTHOR]

The current research aims to improve oral bioavailability, reduce the variability in absorption, and decrease GI intolerance of Nitrofurantoin (NFT) by presenting in a lipid-based liquid self-nanoemulsifying drug delivery system (L-SNEDDS). L-SNEDDS formulations were developed using a thermosolvency technique. Physicochemical properties including in-vitro drug diffusion were exercised to optimize the formula, further, comparative ex-vivo permeability, in-vitro cell line, in-vitro anti-microbial, and in-vivo pharmacokinetic evaluation of optimized formulation was carried out. Based on the highest saturation solubility, soybean oil, oleoyl polyoxyl-6-glycerides, and diethylene glycol monoethyl ether were selected as oil, surfactant, and co-surfactant, respectively. A Smix ratio of 1:2 was selected based on pseudoternary phase diagrams. The formulation prepared with an equal ratio of oil and Smix exhibited the lowest globule size (59.4 ± 0.8 nm), optimum zeta potential (−21.3 ± 1.1 mV), and faster drug release (95.4 ± 4.2 % in 30 min), and hence was selected for further evaluation. Optimized formulation (SF5) was found stable and showed improved membrane permeability against pure drug suspension (1.84 times) and marketed suspension formulation (1.15 times). SF5 exhibited similar % cell viability and % cell toxicity in Caco-2 cell lines compared to the marketed suspension. However, it showed the highest zone of inhibition against both the gram-negative and gram-positive organisms. The relative bioavailability of NFT-loaded L-SNEDDS was enhanced by 1.46 and 1.55 times compared to the marketed and pure drug, respectively. Thus, it can be concluded that the variability of oral absorption is minimized, and oral bioavailability is improved by the novel lipid-based nanocarrier system of NFT. [ABSTRACT FROM AUTHOR]

This study focused on synthesis of anionic magnetite nanoparticles (MNPs) immobilized with a bisphenol A (BPA)-specific peptide aptamer for selective BPA adsorption. The MNP surface was coated with anionic poly(2-acrylamido-2-methylpropane sulfonic acid) (PAMPS) to provide water dispersibility and stability. These nanosorbents, with a saturation magnetization value of 47 emu/g, responded well to the change in zeta potential and hydrodynamic size with varying dispersion pH. The aptamer loading capacity of particles was 0.12 mg/mg MNPs, and the nanosorbents exhibited a 47% BPA adsorption capacity. Importantly, they shown high selectivity in capturing BPA over structurally similar molecules. [ABSTRACT FROM AUTHOR]

This study evaluated the application of carboxylated multi-walled carbon nanotubes (MWCNTs) as a label in immunochromatographic assay for morphine detection. MWCNTs were carboxylated using nitric acid and characterized by Fourier-transform infrared (FTIR) spectroscopy, Raman spectroscopy, field emission scanning microscopy (FESEM), and dynamic light scattering (DLS). The optimum concentration of polyvinyl pyrrolidone (PVP) as a surfactant for homogenous dispersion of MWCNTs was determined by ultraviolet-visible spectroscopy to be 0.5 mg/mL. The zeta potential of MWCNTs before adding PVP was −41.9 ± 1.02 mV, and after adding PVP, −54.1 ± 0.25 mV. On the surface of MWCNTs, the anti-morphine antibody (AM antibody) had a binding effectiveness ranging from 91.1% to 95.5%. The AM antibody-MWCNTs were conjugated to create immunochromatographic test strips. The visual limit of detection (vLOD) was 1.0 ng/mL and the cutoff concentration (COC) was 10.0 ng/mL. Compared to previous study, carboxylated-MWCNTs as a one-dimensional nanomaterial improved the sensitivity of immunochromatographic assay strips and may be utilized to develop the sensitive immunochromatographic assays. [ABSTRACT FROM AUTHOR]

AbstractErlotinib, a potent epidermal growth factor receptor (EGFR) inhibitor, faces bioavailability challenges due to poor water solubility and stability. This study aims to optimize erlotinib-loaded PLGA nanoparticles using a 32 factorial design to enhance drug delivery and therapeutic efficacy. The effects of PLGA concentration (R1) and NaTPP concentration (R2) on nanoparticle characteristics, including particle size, zeta potential, and polydispersity index (PDI), were investigated. The optimal formulation (F5) was identified and characterized, showing a particle size of 169.1 nm, a zeta potential of 20.0 mV, and a PDI of 0.146, indicating uniform and stable nanoparticles. Transmission electron microscopy (TEM) confirmed spherical nanoparticles with minimal aggregation, while X-ray diffraction (XRD) indicated an amorphous state of erlotinib. Formulation F5 demonstrated an entrapment efficiency of 81.9% and a yield of 83.0%. In-vitro drug release studies revealed a sustained release pattern with 90.0% cumulative release at 48 h, following Zero Order kinetics. Cytotoxicity assays showed low cytotoxicity across various cell lines. Statistical analysis confirmed the significant impact of formulation variables on nanoparticle properties. The systematic optimization of erlotinib-loaded nanoparticles has successfully identified formulation F5 as an optimal candidate with favorable characteristics, including minimal particle size, high stability, controlled drug release, and a safe cytotoxicity profile. Notably, the optimized formulation (F5) enhances therapeutic efficacy through improved bioavailability and targeted delivery, addressing the limitations of conventional therapies. These findings suggest that the optimized erlotinib-loaded nanoparticles hold significant potential for enhanced drug delivery and therapeutic efficacy. [ABSTRACT FROM AUTHOR]

This work characterizes microemulsions of Medicago marina essential oil and evaluates their antimicrobial, antibiofilm, and anticoagulant effects. Medicago marina L. aerial parts essential oil was hydro-distilled and analyzed by gas chromatography-FID and gas chromatography/mass spectrometry (GC/MS) for the first time from the Tunisian chemotype. The microemulsion was prepared using an oil/water formulation with a biopolymer (Arabic gum) and surfactant (Tween 20). Antibacterial and antifungal activities were evaluated using the microbroth dilution method, while anticoagulant activity was tested in vitro using prothrombin time (PT) and aPTT tests. Eventually, the binding affinities and molecule’s interactions of the main chemicals with the operational locations of C (30) carotenoid dehydrosqualene synthase and cytidine deaminase were explored. The essential oil contained 71 compounds of which 87.6% were identified. Major compounds were β-ionone (17.67%), 1-methyleugenol (10.75%), eugenol (8.86%), β-damascenone (4.33%), and α-humulene (4.32%). A microemulsion with a diameter of 1.63 μ m, a polydispersity index of 0.17, a zeta potential of –40.8 mV and a pH of 6 was obtained and it showed the highest antibacterial potential against a multitude of microbes, with low MICs varying between 0.406 mg/mL and 3.25 mg/mL. Significant antibiofilm activity was observed with over 80% inhibition at 4 × MIC concentration. It showed better anticoagulant activity than heparin, with PT and aPTT values of 19.5 s and 57 s, respectively, at 10 mg/mL. Molecular docking showed that “(E)-β-ionone” had the highest binding scores. Notable pharmacokinetic and drug-like qualities were found in the obtained molecules after establishing ADME profiling. As a result, Medicago marina L. Essential oil microemulsion can be used in food processing as a preservative. [ABSTRACT FROM AUTHOR]

A novel sanitizer tablet containing clove essential oil (CO) microemulsion was developed. A preformulation study using nuclear magnetic resonance and thermal analyses showed component compatibility. The main components of the samples remained intact despite a color change, probably due to a strong acid-base interaction between eugenol and diethanolamine. The CO microemulsion showed acaricidal and larvicidal activities superior to the commercial product, with product efficacy of 99.9% and larvae mortality of 94%. Optimal spray-drying conditions were achieved with inlet and outlet temperatures of 50°C and 40°C, respectively, an aspiration rate of 1 m3 min⁻1, and a 0.25 L h⁻1 injection flow. The feed suspension comprised 50% (v/v) liquid soap, 37.5% (v/v) water, 12.5% (v/v) ethanol, and 5.0% (w/v) silica. This formulation and processing parameters allowed for successful free-flow powder formation, providing a suitable matrix for incorporating the CO microemulsion via wet granulation without heating. Finally, sanitizer tablets produced from such granules resulted in a uniform product with low weight variation (coefficient of variation of 0.15%), eugenol content of 95.5% ± 3.3, and friability of 0.58%. Furthermore, the tablets showed rapid aqueous dispersion, forming a colloidal system with particle sizes of 221 nm and a zeta potential of -17.2 mV. Antimicrobial activity tests demonstrated the effectiveness of the sanitizer tablet against bacteria and fungi, exhibiting comparable antimicrobial potency to isolated CO. Hence, the sanitizer tablet developed represents a promising candidate as a practical and efficient solution for pest control, offering strong antimicrobial and acaricidal activity. [ABSTRACT FROM AUTHOR]

Treatment of infections caused by Pseudomonas aeruginosa presents a challenge due to its ability to adapt and acquire drug resistance rapidly. Therefore, a key challenge is identifying and investigating new compounds with antibacterial and anti-virulence activity. Tannins, a group of plant polyphenolic compounds, can interact with bacterial cells and their virulence factors. The purpose of this study was to assess the antibacterial potential of using 3,6-bis-O-di-O-galloyl-1,2,4-tri-O-galloyl-β-D-glucose (C55H40O34) isolated from Rhus typhina against P. aeruginosa ATCC BAA-1744. The investigation involved viability analyses using the INT assay, fluorescence analyses of the tannins' interaction with the cell membrane and membrane proteins of P. aeruginosa, and analysis of changes in the Zeta potential. The results obtained allowed us to conclude that C55H40O34 exhibits antimicrobial activity by inducing changes in the biophysical properties of P. aeruginosa's cell membrane. The thermodynamic parameters indicated that C55H40O34 binds to bacterial membrane proteins through hydrophobic interactions. These interactions with proteins may impact their structure and disrupt their functions, such as disturbing or inhibiting the efflux pumps, which are part of P. aeruginosa's resistance mechanisms. Therefore, C55H40O34 may be a new, natural agent and could potentially be used against P. aeruginosa. [ABSTRACT FROM AUTHOR]

This study aimed to assess pumpkin leaves as a protein source and determine the feasibility of these proteins to form complexes with alginate for the encapsulation of folic acid. Different isolation protocols, two based on isoelectric precipitation (one with thermal pretreatment and the other with alkali pre-extraction) and one based on stepwise precipitation with ammonium sulfate, were compared regarding the yield and structural properties of the obtained leaf protein concentrates (LPC). The highest purity of protein was achieved using the thermal-acid protocol and the salting-out protocol at 40% saturation. RuBisCO protein was detected by SDS-PAGE in all LPCs, except for the fractions obtained through salting-out at saturation level ≥ 60%. Complexation of the LPC solutions (1 mg/mL) and sodium alginate solution (10 mg/mL) was monitored as a function of LPC:alginate ratio (2:1, 5:1, and 10:1) and pH (2–8) by zeta-potential measurements and confirmed by FT-IR analysis. Based on the results, the strongest interaction between LPCs and alginate occurred at a pH between 2.20 and 2.80 and an LPC:alginate ratio of 10:1. Complexation resulted in particle yields of 42–71% and folic acid entrapment of 46–92%. The LPC-folic acid interactions elucidated by computational protein–ligand docking demonstrated the high potential of RuBisCO as a biocarrier material for folic acid. The in vitro release study in the simulated gastrointestinal fluids indicated that complexes would be stable in gastric conditions, while folic acid would be gradually released in the intestinal fluids. [ABSTRACT FROM AUTHOR]

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Low molecular weight organic acids (LMWOAs) are common in rhizospheric soil and may impede the interaction between phosphate and metals. Thus, studying how phosphate compounds impact metal immobilization in rhizospheric soil using LMWOAs is crucial. An incubation experiment examined the effects of NaH2PO4 (a P compound) (3%), various concentrations of citric acid (CA), and combinations of P and CA, on soil cadmium (Cd), lead (Pb), and zinc (Zn) immobilization using the European Community Bureau of Reference (BCR) sequential extraction method, CaCl2 extraction method, zeta potential, fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The P, low CA (2 mmol kg–1 soil) (CA2), and P-CA2 treatments reduced acid-soluble and CaCl2-extractable Cd, Pb, and Zn, indicating metal immobilization, with the P-CA2 treatment being the most effective. High CA (>5–20 mmol kg–1 soil) or a P with high CA reversed prior patterns, suggesting metal mobilization. The zeta potential study indicated that when pH increased, treatments became more negative, notably P-CA2 followed by P, suggesting that electrostatic adsorption was the predominant metal immobilization mechanism, especially in P-CA2. XRD tests, however, showed that the P treatment alone produced Cd phosphate, pyromorphite, and hopeite, indicating that sorption and precipitation were the main metal immobilization processes in the P treatment alone. In conclusion, P-CA2 was found to be the most efficient metal immobilization and redistribution treatment for contaminated soils. Rhizospheric CA may alter Cd, Pb, and Zn mineral stability. Therefore, when treating Cd, Pb, and Zn-contaminated soils with a P compound, CA should be addressed. [ABSTRACT FROM AUTHOR]

Introduction: Conventional chemotherapy treatment is commonly linked to significant side effects due to high therapeutic doses. In this regard, nanoformulations with chemotherapeutic medications hold promise in enhancing drug effectiveness through the reduction of therapeutic dosages, thereby mitigating the potential for adverse side effects. Because of numerous applications in the biomedical arena, there has been a rising interest in developing an environmentally acceptable, long-lasting, and affordable technique for the production of gold nanoparticles. In this particular context, the incorporation of plant extracts in the production of metallic nanoparticles has garnered the interest of numerous scholars. Here, we report the synthesis of gold particles by the green method using Cannabis sativa L. leaf extract and their conjugation with doxorubicin. Methods: The gold nanoparticles were synthesized by using Cannabis sativa extract and were characterized with various biophysical techniques. Subsequently, gold nanoparticles were conjugated with doxorubicin and their efficacy was tested on A549 cells. Results and Discussion: The biogenic synthesis of gold nanoparticles was ascertained through an absorption peak at a wavelength of 524 nm, and it was shifted to 527 nm when conjugated with doxorubicin. Nanoparticles were found to be stable exhibiting a zeta potential value of −20.1 mV, and it changed to −12.7 mV when loaded with doxorubicin. The hydrodynamic diameter of nanoparticles was determined to be 45.64 nm and it was increased to 58.95 nm when conjugated with the drug. The average size of nanoparticles analyzed by TEM was found to be approximately 17.2 nm, while it was 23.5 nm in the case of drug-nanoconjugate. Moreover, there was a significant amelioration in the antiproliferative potential of doxorubicin against lung cancer A549 cells when delivered with gold nanocarrier, which was evident by the lower IC50 and IC75 values of drug-nanoconjugates in comparison to drug alone. Furthermore, the inhibitory effect of drug-nanoconjugates and drug alone was characterized by alteration in the cell morphology, nuclear condensation, increased production of reactive oxygen species, abrogation of mitochondrial membrane potential, and enhanced caspase activities in A549 cells. In sum, our results suggested enhanced efficacy of doxorubicin-gold nanoconjugates, indicating effective delivery of doxorubicin inside the cell by gold nanoparticles. [ABSTRACT FROM AUTHOR]

AbstractThis study focused on developing and evaluating dasatinib-loaded nanoparticles (DST-NPs) using Eudragit L100 as a polymer matrix for enhanced breast cancer treatment. The optimized formulation exhibited a particle size of 202.1 ± 5.7 nm, a zeta potential of −18 ± 1.01 mV, and an entrapment efficiency of 93.11 ± 0.2%. In-vitro release studies demonstrated sustained drug release from DST-NPs, following Fickian diffusion. Pharmacokinetic studies in rats revealed higher Cmax and AUC0-t for DST-NPs compared to pure DST, indicating improved bioavailability. Tissue distribution studies showed enhanced targeting of DST-NPs, with higher concentrations in the liver and spleen. In vivo efficacy in a DMBA-induced mammary carcinoma model demonstrated that DST-NPs significantly reduced tumor volume, maintained stable body weight, and improved survival rates compared to pure DST. Hematologic analysis indicated a favorable blood profile with DST-NPs, and histopathological examinations confirmed the restoration of normal mammary gland and liver architecture. MTT assays showed higher cytotoxicity of DST-NPs against MCF-7, MDA-MB231, and 4T1 cell lines, with lower IC50 values than pure DST. Stability studies indicated that DST-NPs maintained their properties over six months at various storage conditions. These findings highlight the potential of DST-NPs as an effective nanocarrier system for cancer therapy. [ABSTRACT FROM AUTHOR]

Two strategies were employed to modify the performance of the nano-niosome drug delivery system. Initially, the surface of the nano-niosomes underwent modification through the inclusion of polyethylene glycol, thereby altering its properties. Additionally, the core of the nano-niosomes was equipped with Fe3O4 magnetic nanoparticles to impart magnetic characteristics to the system. This study presents the development of PEGylated magnetic nanoniosomes (PMNios) for the co-delivery of artemisinin (ART) and metformin (MET) in cancer therapy, highlighting significant advancements in chemotherapeutic efficacy. The magnetization of the nano-niosomes facilitated the targeted delivery of drugs to specific tissues, while PEGylation improved the bioavailability of the nano-niosomes. These PEGylated magnetic niosomes (PMNios) were then loaded with artemisinin and metformin drugs. The synthesized PMNios were thoroughly evaluated in terms of zeta potential, size, morphology, and entrapment efficiency. The PMNios achieved a drug loading efficiency of 88%. They exhibited an average size of 298 nm, a polydispersity index of 0.32, and a zeta potential of − 19 mV, indicating the complete stability. SEM and TEM images of the PMNios revealed a spherical morphology. Subsequently, the PMNios were compared with other forms of nano-niosomes, including empty niosomes, non-magnetic niosomes, and non-PEGylated niosomes. The encapsulation of the nano-niosomes with magnetic nanoparticles allows for faster delivery of the encapsulated drugs to the tumor site, while PEGylation improved the stability, bioavailability, and controlled release of the PMNios. Furthermore, the in-vitro effectiveness of various formulations of the PMNios against A549, a lung cancer cell line, demonstrated that the PMNios exhibited appropriate toxicity towards cancer cell lines in the presence of an external magnetic field. Gene expression level of Bcl2 were lower for the PMNios-ART-MET system, whereas the level of Bax were higher than the other group. The PMNios-ART-MET system also demonstrated well internalization into the A549 cells and preponderant endocytosis. These findings underscore the novelty and potential of PMNios as a robust platform for the targeted co-delivery of hydrophilic and hydrophobic drugs, promising a new frontier in cancer therapy by enhancing the therapeutic index and minimizing side effects. [ABSTRACT FROM AUTHOR]

ABSTRACT Adding plant extracts to sausage and other meat products is very important to improve their quality, safety, and durability. The aim of this study was to evaluate the microbiological properties of beef sausage enriched with roselle (Hibiscus sabdariffa L.) sepal extract. The total content of phenolic and flavonoid compounds in hydroalcoholic extract of Roselle sepals was measured by Folin‐Ciocalteu test and aluminum chloride colorimetric method, and antioxidant activity was measured by DPPH method. Pectin was used to encapsulate the extract. The characteristics of capsules, including particle size, zeta potential, and capsule efficiency were measured. Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of extracts were performed by tube dilution method. Microbial tests were performed on sausage treatment samples. Analysis of the obtained data was done using SPSS and Excel software. The study revealed that the total phenolic and flavonoid compounds in the extract were 174.6 mg of gallic acid per gram and 16.8368 mg of quercetin, respectively. The extract displayed the highest antioxidant activity at elevated concentrations. Particle size ranged from 16.833 to 640.534 μm. The zeta potential and capsule efficiency were found to be satisfactory. Compared to the encapsulated extract, the free roselle extract better inhibited Staphylococcus aureus (s. aureus), Salmonella typhimurium (S. typhimurium), and Escherichia coli (E.coli). During storage until day 20, these bacteria did not grow in the free or encapsulated extract groups. However, S. aureus appeared in the free extract group from day 25 and the encapsulated extract group from day 20. Roselle extract has antimicrobial properties that can improve the quality and safety of beef sausage during storage. [ABSTRACT FROM AUTHOR]

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Introduction: This study aimed to prepare cholesterol and stearic acid-based solid lipid nanoparticles of gabapentin (GAB-SLNs) for protection against streptozotocin (STZ)-induced retinal injury in rats. Methods: We prepared four preparations of GAB-SLNs using a hot high-shear homogenization ultrasonication process, and the best formulation was selected and tested for biological activity. The retinal injury was brought in male adult albino rats while gabapentin doses continued for 6 weeks. Six groups of rats were assigned as the vehicle, diabetic, diabetic + gabapentin (10–20 mg/kg), and diabetic + GAB-SLNs (10–20 mg/kg). GAB-SLN#2 was selected as the optimized formulation with high entrapment efficacy (EE%, 98.64% ± 1.97%), small particle size (185.65 ± 2.41 nm), high negative Zeta potential (−32.18 ± 0.98 mV), low polydispersity index (0.28 ± 0.02), and elevated drug release (99.27% ± 3.48%). The TEM image of GAB-SLN#2 revealed a smooth surface with a spherical shape. Results: GAB-SLNs provided greater protection against retinal injury than free gabapentin as indicated by the histopathology data which demonstrated more organization of retinal layers and less degeneration in ganglion cell layer in rats treated with GAB-SLN#2. Further, GAB-SLN#2 reduced the inflammatory proteins (IL-6/JAK2/STAT3) and vascular endothelial growth factor (VEGF). Conclusion: The preparation of GAB-SLNs enhanced the physical properties of gabapentin and improved its biological activity as a neuroprotectant. Further studies are warranted to validate this technique for the use of oral gabapentin in other neurological disorders. [ABSTRACT FROM AUTHOR]

The current research involved the synthesis of zinc oxide nanoparticles (ZnO-NPs) using an aqueous extract of Helichrysum cymosum shoots, and subsequent characterization via different analytical methods, such as UV–Vis spectroscopy, Scanning electron microscope (SEM), Energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Transmission electron microscope (TEM), and zeta potential. The biological effects of the ZnO-NPs were then tested against C3A hepatocyte cells and L6 myocyte cell lines via series of analysis, including cytotoxicity, antioxidant, anti-inflammatory, and antidiabetic effect via enzymatic inhibition. The UV–Vis analysis showed a maximum absorption spectrum at 360, and the TEM analysis reveals a spherical and hexagonal structures, with an average dimension of 28.05–58.3 nm, and the XRD reveals a crystalline hexagonal structure. The zeta potential evaluation indicated that the ZnO-NPs are relatively stable at − 20 mV, and the FTIR analysis identified some important functional group associated with phenolics, carboxylic acid, and amides that are responsible for reducing and stabilizing the ZnO-NPs. The synthesized ZnO-NPs demonstrated cytotoxic effects on the cell lines at higher concentrations (125 µg/mL and 250 µg/mL), complicating the interpretation of the results of the inflammatory and antioxidant assays. However, there was a significant (p < 0.05) increase in the inhibitions of pancreatic lipase, alpha-glucosidase, and alpha-amylase, indicating beneficial antidiabetic effects. [ABSTRACT FROM AUTHOR]

The sluggish rate of the anode oxygen evolution reaction (OER) is a major bottleneck for green hydrogen production, making a room-temperature alkaline water electrolyser critical to unlocking the full potential of this technology. Using a perovskite oxide as an electrochemical matrix and forming a self-assembled oxyhydroxide (OOH) layer on the surface via a self-reconstruction activation process (SRAP) is a promising strategy to enhance OER catalytic activity. However, the mechanistic details and long-term impact of SRAP, especially its relationship to catalytic activity, oxygen collection efficiency, and catalyst dissolution, are not fully understood. To address this knowledge gap, we used layered double perovskite (LDP) PrBa 0 · 75 Ca 0 · 25 Co 1 · 5 Fe 0 · 5 O 5+δ (PBCCF) and PrBa 0 · 75 Ca 0 · 25 Co 1 · 5 Fe 0 · 4 Ni 0 · 1 O 5+δ (PBCCFN) as model electrochemical catalysts and then triggered SRAP. Subsequently, chronoamperometry (CA), rotating ring disk electrode (RRDE) and in-situ electrochemical quartz crystal microbalance (EQCM) were used to study the effect of the Ni-doping on PBCCF SRAP in terms of catalytic activity, oxygen collection efficiency and catalyst stability. The results showed that the OER catalytic current of the LDP PBCCF and PBCCFN was enhanced via SRAP and the oxygen collection efficiency can be maintained, suggesting that the increase in catalytic current is attributed to OER catalytic activity increase rather than electrochemical catalyst dissolution. Additionally, the effect of the catalytic activity enhancement was more significant in PBCCFN. More importantly, the stability of the LDP PBCCF and PBCCFN after SRAP are higher than simple perovskite Ba 0 · 5 Sr 0 · 5 Co 0 · 8 Fe 0 · 2 O 3-δ (BSCF) because of the increase in the redeposition rate. The observations suggest that using LDP PBCCF and PBCCFN as matrices followed by triggering SRAP can provide valuable insights for designing LDP based OER electrocatalysts. Synopsis: The influence of Ni-doping on DLP SRAP was studied in terms of catalytic activity, faradaic efficiency and stability. [Display omitted] • I nnovative DLP Catalyst: Developed a novel Ni-doped DLP catalyst for enhanced OER efficiency and stability. • Mechanistic Understanding: Utilized in-situ techniques to investigate the catalyst's structural changes and OER pathways. • Dual OER Improvement: Achieved both increased activity and durability, addressing the trade-off in OER catalysts. [ABSTRACT FROM AUTHOR]

The study aimed to apply biosilica nanoparticles from renewable resources for improving soil quality as a type of fertilizer carier. The silica particles having a purity of about 98 % were extracted from rice husk at the calcination temperatures of 550 °C, 600 °C, 650 °C, and 700 °C. The required materials properties were investigated by advanced measurement techniques. All samples showed the amorphous structure with Si–O–Si bond and the particles' agglomeration with the average size of 10–50 nm and principle electronic structures with the typical spectra of Si and O 2. When the synthesized silica was used as the medium to release absorbed nutrients in a controlled manner, surface properties, including the Brunauer–Emmett–Teller area and the average pore diameter were evaluated between 179 m2/g to 570 m2/g, and 4 nm–40 nm, respectively. The measured electrokinetic potential of the synthesized particles was between −20 mV and −36 mV guaranteeing the stability when they are dispersed in the aqueous environment. The experimental results showed that the silica particles calcinated at 650 °C had the best properties. [ABSTRACT FROM AUTHOR]

Paclitaxel (PTX), a naturally occurring diterpenoid isolated from Taxus brevifolia, is a first-line drug for the treatment of glioblastoma; however, it suffers from the disadvantages of poor water solubility and nonspecific biodistribution, which cause serious side effects in the human body. The marketed formulation suffers from serious side effects, such as allergic reactions, neutropenia, and neuropathy, which require safe and effective formulations of PTX. In the present study, PTX was entrapped in a solid–liquid lipid mixture with the aid of a surfactant using a modified solvent evaporation technique. Higher entrapment of the impressive stability of the formulation was achieved by employing quality design-based strategies. Optimized levels by employing a numerical optimization technique for each factor, that is, surfactant concentration (X1), lipid concentration (X2), and amount of organic solvent (X3) were 0.3%, 0.76% & 8.3 ml respectively. The resultant formulation exhibited a particle size of 121.44 nm, entrapment efficiency of 94.27%, and zeta potential of −20.21 mV with unimodal size distribution. A reduction in the % crystalline index from 48 to 3.4% ensured the amorphous form of the entrapped drug inside the formulation, which precludes the fear of leakage and instability of the formulation. Cell line studies conducted on U87MG Cell lines also suggested that the NLC of paclitaxel are more effective than those of pure PTX. In summary, PTXNLC seem to be a superior alternative carrier system for the formulation industry to obtain higher entrapment with excellent stability. [ABSTRACT FROM AUTHOR]

The use of nanosized particles is becoming more popular for the topical treatment of skin conditions. In this research work, we created and investigated the effects of solid lipid nanoparticles (SLN) containing hyaluronic acid and tretinoin. Solvent emulsification diffusion method was used to prepare the SLN formulation and characterized for their physicochemical properties. Fourier transform infrared spectroscopy was used to confirm that hyaluronic acid and tretinoin were incorporated in the SLN. Furthermore, X-ray diffractogram, thermal analysis including DSC and TGA and in vitro dissolution, permeation tests were also performed along with microbial assessment. Clinical studies in human were performed to evaluate the effect of the SLN on skin wrinkles. The SLN was 750 ± 31.29 nm in size, with a zeta potential of 13.07 ± 0.75 mV and a narrow polydispersity index of 0.24 ± 0.12. The entrapment efficiency of tretinoin was found to be 90.07 ± 4.79%. Clinical studies in healthy human volunteers demonstrated that 90% of the tested individuals had improved skin conditions (reduction in wrinkles), by at least one grade after 4 weeks of treatment. Regarding the development on SLN, it was found that the internal phase concentration did not considerably affect the physicochemical and microbiological properties. Therefore, Hyaluronic acid has potential for the development of SLN applicable to cosmetic formulations, especially for skin. These findings show that the developed SLN have potential for use as cosmetics in the future. [ABSTRACT FROM AUTHOR]

Background/Objectives: The aims of the presented study were the development of four types of silibinin-loaded liposomes (multilamellar liposomes—MLVs, sonicated small unilamellar liposomes—SUVs, UV-irradiated liposomes, and lyophilized liposomes) and their physicochemical characterization and biological potential related to skin health benefits. Methods: The characterization was performed via the determination of the encapsulation efficiency (EE), particle size, polydispersity index, zeta potential, conductivity, mobility, storage stability, density, surface tension, viscosity, FT-IR, and Raman spectra. In addition, cytotoxicity on the keratinocytes and antioxidant and anti-inflammatory potential were also determined. Results: UV irradiation significantly changed the rheological and chemical properties of the liposomes and increased their cytotoxic effect. The lyophilization of the liposomes caused significant changes in their EE and physical characteristics, decreased their ABTS and DPPH radical scavenging potential, and increased their potential to reduce the expression of interleukin 1 beta (IL-1β) in cells treated with bacterial lipopolysaccharide. Sonication significantly changed the EE and physical and rheological properties of the liposomes, and slightly increased their cytotoxicity and reduction effect on IL-1β, while the anti-ABTS and anti-DPPH capacity of the liposomes significantly increased. All developed liposomes showed an increasing trend in particle size and a decreasing trend in zeta potential (absolute values) during storage. Conclusions: Silibinin-loaded liposomes (MLVs and lyophilized) showed promising antioxidant activity (toward reactive oxygen species generated in cells) and anti-inflammatory effects (reducing macrophage inhibitory factor expression) on keratinocytes and did not lead to a change in their viability. Future perspectives will focus on wound healing, anti-aging, and other potential of developed liposomes with silibinin in sophisticated cell-based models of skin diseases, wounds, and aging. [ABSTRACT FROM AUTHOR]

Background/Objectives: Trans-resveratrol (Res) has been reported to possess many biological activities, including neuroprotective effects, owing to its anti-inflammatory and antioxidant properties. However, Res has very low water solubility, which limits its therapeutic application. In this work, we formulated water-soluble micellar formulations incorporating Res using polyethylene glycol monostearate (stPEG). Methods: These formulations (stPEG/Res) were developed using five types of stPEG containing 10, 25, 40, 55 and 140 PEG repeat units. The formulations were characterized for Res content, water solubility, particle size, zeta potential, precipitation, biodistribution, and efficacy against neuronal and motor dysfunction in intracerebral hemorrhage (ICH). Results: Intravenous administration of stPEG40/Res, which demonstrated particle size, water solubility, and biodistribution properties suitable for intravenous administration, suppressed neurological and motor dysfunction following in a collagenase-induced ICH mouse model. These effects were inhibited by zinc protoporphyrin-9, an inhibitor of the antioxidant enzyme heme oxygenase-1, suggesting that Res contributes to antioxidant enzyme expression and anti-inflammatory activity. Conclusions: The stPEG/Res micellar formulation developed in this study may offer a promising therapeutic approach for ICH treatment. [ABSTRACT FROM AUTHOR]

Background: This study introduces a novel dexamethasone (DEX) mixed micellar system (DEX-MM) using Soluplus® and Pluronic F-127 (PF127) to enhance ocular drug delivery. The enhancement of ocular application properties was achieved by creating a chitosan-coated DEX-MM (DEX-CMM), which promotes better adherence to the ocular surface, thereby improving drug absorption. Methods: Using the solvent evaporation method, a formulation was developed with a Soluplus®-to-drug ratio of 1:10, enhanced with 0.25% PF127. After dispersing in water, 1% chitosan (CS) was added. The stability and integrity of DEX within the micelles were verified using attenuated total reflection–Fourier transform infrared spectroscopy (ATR-FTIR) and differential scanning calorimetry (DSC). Additionally, in vitro and ex vivo drug release studies were conducted. Results: DEX-CMM (F6) demonstrated a particle size of 151.9 ± 1 nm and a polydispersity index (PDI) of 0.168 ± 0.003, suggesting uniformity and high electrostatic stability with a zeta potential of +35.96 ± 2.13 mV. The non-Fickian drug release mechanism indicated prolonged drug retention. Comparative analyses showed DEX-CMM outperforming a standard DEX suspension in drug release and ocular tissue permeation, with flux measurements significantly higher than the DEX suspension. Conclusion: The study confirmed the efficacy of DEX-CMM in enhancing drug delivery to ocular tissues, evidenced by improved permeability. Safety evaluations using the HET-CAM test demonstrated that DEX-CMM was non-irritant, supporting its potential for effective ocular drug delivery. [ABSTRACT FROM AUTHOR]

Background: Gene therapy can be viewed as a promising/valuable therapeutic approach directed to cancer treatment, including glioblastoma. Concretely, the combination of gene therapy with chemotherapy could increase its therapeutic index due to a synergistic effect. In this context, bovine serum albumin (BSA)-coated temozolomide (TMZ)-peptide (WRAP5)/p53 gene-based plasmid DNA complexes were developed to promote payload co-delivery. Methods: Design of experiments (DoE) was employed to unravel the BSA-coated TMZ-WRAP5/p53 nanocomplexes with the highest potential by considering the nitrogen to phosphate groups ratio (N/P), and the BSA concentration as inputs and the size, polydispersity index, surface charge and p53-based plasmid complexation capacity (CC) as DoE outputs. Results: The obtained quadratic models were statistically significant (p-value < 0.05) with an adequate coefficient of determination, and the correspondent optimal points were successfully validated. The optimal complex formulation had N/P of 1.03, a BSA concentration of 0.08%, a size of approximately 182 nm, a zeta potential of +9.8 mV, and a pDNA CC of 96.5%. The optimal nanocomplexes are approximately spherical. A cytotoxicity assay showed that these BSA-coated TMZ-WRAP5/p53 complexes did not elicit toxicity in normal brain cells, and a hemolysis study demonstrated the hemocompatibility of the complexes. The complexes were stable in cell culture medium and fetal bovine serum and assured pDNA protection and release. Moreover, the optimal BSA-coated complexes were able of gene transcription and promoted a significant inhibition of glioblastoma cell viability. Conclusions: The reported findings instigate the development of future research to evaluate their potential utility to TMZ/p53 co-delivery. The DoE tool proved to be a powerful approach to explore and tailor the composition of BSA-coated TMZ-WRAP5/p53 complexes, which are expected to contribute to the progress toward a more efficient therapy against cancer and, more specifically, against glioblastoma. [ABSTRACT FROM AUTHOR]

Background/Objectives: Nanoemulsions (NEs) possess properties that enhance the solubility, bioavailability and therapeutic efficacy of drugs. Chalcones are compounds known for their antifungal properties. In this study, we evaluated different emulsification techniques to create alginate nanoemulsions containing chalcone (1E,4E)-1,5-bis (4-methoxyphenyl) penta-1,4-dien-3-one (DB4OCH3). Our goal was to develop an antifungal formulation targeting Candida albicans strains. Methods: Ultrasound and ultrasound combined with high-speed homogenization techniques were used to prepare alginate-stabilized nanoemulsions. Particle size, zeta potential and encapsulation efficiency were evaluated. Additionally, in vitro release studies were conducted. Results: The combined emulsification technique produced stable nanoparticles with high encapsulation efficiency and antifungal activity, with a minimum inhibitory concentration of 8.75 μg/mL for the nanoemulsions compared to 312 µg/mL for free DB4OCH3. NEs' effectiveness can be attributed to their ability to form nanodroplets efficiently, facilitating the solubilization of the chalcone in the oily phase. The particle size varied between 195.70 ± 2.69 and 243.40 ± 4.49 nm, with an increase in chalcone concentration leading to larger particle sizes. The zeta potential showed values from −91.77 ± 5.58 to −76.90 ± 4.44 mV. The UHS-7 sample exhibited an encapsulation efficiency of 92.10% ± 0.77, with a controlled in vitro release of 83% after 34 h. Molecular docking simulations showed that the aromatic nature of DB4OCH3 resulted in the formation of apolar interactions with aromatic residues located in the active site of the TMK, as observed in their respective co-crystallized inhibitors, within an affinity energy range that enables optimum specificity of the ligand for these two pathways. Pharmacokinetic analyses indicated high passive cell permeability and low hepatic clearance, and phase I metabolism reduces its oral bioavailability and metabolic stability, suggesting a promising active ingredient as an oral drug with control of the daily oral dose administered. Conclusions: The combined nanoemulsification technique led to the formation of finely dispersed nanodroplets that favored the solubilization of the chalcone in the oil phase, which led to a better performance in the antifungal properties. DB4OCH3 shows promise as an oral drug with controlled dosing. [ABSTRACT FROM AUTHOR]

Background: Voriconazole is an antifungal drug, which is classified under Bio-Classification System-II and has low water solubility (0.71 mg/mL) and high permeability. Hardly any endeavors have been made to increase the bioavailability of voriconazole. Objective: To develop and evaluate a solid SMEDDS (self-microemulsifying drug delivery system) for antifungal activity. Methods: Based on solubility studies of Labrafil-M 1994 CS (oil), Cremophor-RH 40 (a surfactant) and Transcutol-HP (a co-surfactant) were selected as components of the SMEDDS and a pseudo-ternary phase diagram was prepared. Thereafter, the oil, surfactant, and co-surfactant were mixed with altered weight ratios (1:1/1:2/2:1) and evaluated through various in vitro, in vivo analyses. Results: The particle size of the optimized formulation was observed to be 19.04 nm and the polydispersity index (PDI) value was found to be 0.162 with steady-state zeta potential. The optimized liquid SMEDDS was converted into a solid SMEDDS. Various adsorbents, such as Aerosil-200, Avicel-PH101, Neusilin-US2, and Neusilin UFL2 were screened to better detect the oil-absorbing capacity and flow properties of the powder. Neusilin UFL2 was selected as an adsorbent due to its better oil-absorbing capacity. DSC, X-ray diffraction, and dissolution studies were carried out to characterize the formulation. Further, the Pharmacokinetic profile was also studied in Wistar rats and the Cmax, tmax, and AUC0→t were calculated. The Cmax and AUC0→t plasma concentration is considerably better for the SMEDDS than for the pure drug and marketed formulation. Conclusions: This investigation clearly reveals the potential of developing a solid SMEDDS for candidiasis and invasive aspergillosis treatment, with better efficacy as compared to the commercially available marketed formulation. [ABSTRACT FROM AUTHOR]

In recent years, nonconventional sources have been explored for the extraction of starch due to their potential applications. Thus, this study investigates the potential of loquat seeds starch and exploring their structural and thermal properties. Moreover, the nanoemulsion is prepared from starch, flax seed oil, and tween 80 which is further utilized as a coating for the shelf‐life improvement of citrus fruits such as strawberries. The yield of loquat seed starch is 30.04% ± 2.19% with a particle size of 160.4 ± 4.06 nm and −16.2 ± 1.45 mV zeta potential. The gelatinization temperature of starch is observed to be 78.75 °C. Starch samples show major peaks at 3287.52, 2929.52, 1642.07, 1339, 1149.68, 1077.79, and 1003.62, 859.62, 573.01, and 526.25 cm−1. X‐ray diffraction reveals the semicrystalline structure of starch. The characterization of nanoemulsion reveals its excellent structural properties and stability. When the nanoemulsion is coated on strawberries, it effectively delays weight loss and also affects the titratable acidity content and total soluble solids, thereby reducing spoilage. In conclusion, this study demonstrates that the nanoemulsion exhibits great potential in the shelf‐life improvement of strawberries. Thus, combining oils with starch represents a promising approach to enhance its effectiveness in controlling foodborne pathogens. [ABSTRACT FROM AUTHOR]

In present study, the effects of orange peel essential oil and ultrasonic treatment on properties of corn starch based edible coating and films including their effects on the shelf life of citrus (Kinnow) fruits are investigated. The ultrasonic approach and essential oil significantly improves the quality characteristics of edible coating formulations, stability, and rheological behaviour of coating materials by reducing the particle size, including antimicrobial activity. The particle size of the coating materials reduces from 2495 nm (control) to 298.8 nm by ultrasonication treatment with improved stability (−39.251 mV) as well as antimicrobial activity. The tensile strength (720 N) and solubility (32.40%) of the CSEOU edible film are also improved as compared to CSEO and CS edible films. The coating formulation enriched with essential oil and ultrasonic treatment (CSEOU) improves the shelf‐life of Kinnow by retarding weight loss (PLW) and microbial load, as well as maintaining higher acidity (TA), total soluble solids (TSS), and higher antioxidant activity. CSEOU treated samples indicate lowest weight loss (24.57%), pH (3.89) with higher TA (3.999%), firmness (494.229 N), phenolic (26.17 mg 100 g−1), flavonoid (34.11 mg 100 g−1), antioxidant (49.04%), and antimicrobial activity against A. niger, E. coli and S. aureus as compared to other samples. [ABSTRACT FROM AUTHOR]

In this study, the synthesis and characterization of the fluorescent metal–organic framework (MOF)‐polymer composites is reported based on zirconium‐based MOFs (UiO‐66 and UiO‐66(OH)₂) and a conjugated polyelectrolyte, poly(phenylene ethynylene) carboxylate (PPE‐CO₂‐108). The defect‐rich nature of these Zr‐MOFs facilitates strong interactions between the polyelectrolyte's carboxylic acid moieties and the open metal sites on the Zr clusters within the MOF nanoparticles. The composites are prepared by a simple impregnation approach, where MOF nanocrystals suspended in HEPES buffer are added to the polymeric solution under sonication for 10 min. The obtained MOF composites (i.e., UiO‐66‐CPE and UiO‐66 (OH)2‐CPE) are characterized using powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer‐Emmett‐Teller (BET) surface area, zeta potential measurements, and UV–vis spectroscopy. The characterization confirmed the homogeneous distribution of the MOF nanocrystals on the polymer as seen in the SEM images, and the interaction with PPE‐CO₂‐108 is confirmed by the decrease in the surface areas from 1050 to 590 m2 g−1 for UiO‐66‐CPE and from 500 to 137 m2 g−1, for UiO‐66(OH)2‐CPE. Fluorescence microscopy revealed strong fluorescence in the microparticles, confirming robust polymer‐MOF interaction. The composites also exhibit improved photostability of the conjugated polyelectrolyte, suggesting their potential for applications in biomedical imaging and other areas requiring stable and bright fluorescent systems. [ABSTRACT FROM AUTHOR]

This study presents the development and evaluation of a DFO@mAb‐NP (DFO@Durvalumab‐HSA‐DTX nanoparticle) nanoplatform for imaging in triple‐negative breast cancer (TNBC). The nanoplatform demonstrated significant changes postconjugation with DFO, evidenced by increased particle size from 178.1 ± 5 nm to 311 ± 26 nm and zeta potential alteration from −31.9 ± 3 mV to −40.5 ± 0.8 mV. Fourier‐transform infrared spectroscopy and ultraviolet spectral analyses confirmed successful DFO conjugation, with notable shifts in peak wavelengths. High labeling efficiency was achieved with 89Zr, as indicated by thin layer radio chromatography and high‐performance liquid radio chromatography results, with labeling efficiencies of 98 ± 2% for 89Zr‐DFO@mAb and 96 ± 3% for 89Zr‐DFO@mAb‐NP. The nanoplatforms maintained stability over 24 h, showing less than 5% degradation. Lipophilicity assays revealed logP values of 0.5 ± 0.03 for 89Zr‐DFO@mAb‐NP and 0.98 ± 0.2 for 89Zr‐DFO@mAb, indicating a higher lipophilic tendency in the radiolabeled Durvalumab. Cell uptake experiments showed an initial high uptake in MDA‐MB‐468 cells (45.1 ± 3.2%), which decreased over time, highlighting receptor‐specific interactions. These comprehensive findings suggest the promising potential of the DFO@mAb‐NP nanoplatform for targeted imaging in TNBC, with implications for improved diagnostic accuracy and treatment strategies. [ABSTRACT FROM AUTHOR]

It is well known that zinc oxide (ZnO) is recognized as a highly effective and stable inorganic antibacterial material. The dispersibility and microstructure of ZnO play crucial roles in determining its antibacterial activity. In this investigation, we successfully synthesized ZnO nanoparticles with exceptional dispersibility and potent antibacterial properties through ultrasonic sonication, utilizing sodium hexametaphosphate, sodium dodecyl benzene sulfonate, and sodium polyacrylate as effective dispersants. To comprehensively assess the impact of these dispersants on the structure and morphology of the ZnO nanoparticles, various characterization techniques, including X-ray diffraction analysis, transmission electron microscopy imaging, Fourier transform infrared spectroscopy, thermogravimetric analysis, UV‒Vis absorption spectroscopy, X-ray photoelectron spectroscopy, and zeta potential analysis, were employed. The average particle sizes calculated for ZnO-SHMP, ZnO-SDBS, and ZnO-PAAS are approximately 300 nm. The zeta potential of ZnO-SHMP, ZnO-SDBS, and ZnO-PAAS are − 18.67, -12.77, and − 16.77 mV, which is significantly lower than that of the pristine ZnO (-2.01 mV). Our findings demonstrate that the addition of dispersants significantly enhances the dispersibility of ZnO nanoparticles while also improving their antibacterial efficacy against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) by achieving an antibacterial rate exceeding 99%. It's observed that the introduction of dispersants led to morphological changes in the ZnO particles, contributing to their enhanced antibacterial activity. Compared with dark conditions, particularly under fluorescent lamp irradiation, superior antibacterial effects were achieved. Mechanistically, our findings suggest that the synergistic effect of the ZnO-bacteria interaction, along with soluble Zn2+ ions and the generation of reactive oxygen species, accounts for the observed antibacterial efficacy. The average contents of ZnO-PAAS released Zn2+ in the liquid culture media of E. coli and S. aureus were 27.5 mg/L and 41.1 mg/L, respectively, higher than that of the pristine ZnO. The incorporation of ZnO, which is prepared with a dispersant, into waterborne paint yields a pronounced antibacterial effect, rendering it highly promising for practical applications such as antibacterial coatings. [ABSTRACT FROM AUTHOR]

Objective: This study looked at how different concentrations of curcumin (Curc), zinc chloride (ZnCl2), zinc oxide nanoparticles (ZnO‐NPs) and Curc loaded on ZnO‐NPs (Curc‐co‐ZnO‐NPs) in cryopreservation dilution affected the quality of ram sperm after thawing. Methods: ZnO‐NPs were synthesised using Berberis vulgaris leaf aqueous extract. Then, Curc was loaded on the ZnO‐NPs that had been synthesised. We used analytical methods to look at the composition, morphology and size of green synthesised ZnO‐NPs and Curc‐co‐ZnO‐NPs, including UV‐Vis, zeta potential, EDX, DLS, FE‐SEM and FT‐IR. Using a Tris‐base extender containing various concentrations of Curc, ZnCl2, ZnO‐NPs and Curc‐co‐ZnO‐NPs (0, 1, 10 and 100 µg/mL), semen samples from four rams were combined. Sperm motility, viability, DNA and plasma membrane integrity, total abnormalities and malondialdehyde (MDA) generation were all evaluated in treatment groups after thawing. Results: The results showed that adding 1 µg/mL of ZnO‐NPs and Curc‐co‐ZnO‐NPs significantly reduced the level of MDA and total abnormalities (p < 0.05). Additionally, following the freeze‐thawing procedure, the presence of 1 µg/mL of Curc‐co‐ZnO‐NPs in the diluent of ram sperm significantly increased the percentage of sperm viability and motility in comparison to the control and other treatment groups (p < 0.05). Furthermore, as compared to the control group and other treatments, treatments containing 1 µg/mL of Curc‐co‐ZnO‐NPs significantly improved membrane and DNA integrity (p < 0.05). Conclusions: It appears that following freeze‐thawing, the Curc‐co‐ZnO‐NPs (1 µg/mL) enhanced sperm parameters. [ABSTRACT FROM AUTHOR]

Berberine hydrochloride (BH) extracted from Coptis chinensis (CC) and Matrine (MT) separated from Sophora flavescens (SF) are alkaloids with potent anti-bacterial, anti-inflammatory, and anti-tumor effects. Motivated by the clinical practice of using CC and SF together, we aimed to demonstrate that the synergistic application of the natural compounds BH and MT could enhance therapeutic effects and minimize side effects. Two types of liposomes, liposomes containing only BH (BH-LP) and liposomes containing both BH and MT (BH-MT-LP), were successfully prepared via the reverse evaporation method. The liposome preparation process was optimized by single-factor screening and the Box–Behnken experimental design method. The results showed that the liposomes had particle sizes in the range of 222.7 to 235.4 nm, polydispersity indicated in the range of 11.8% to 23.3%, and zeta potentials in the range of −35.9 to −31.1 mv. BH-MT-LP showed superior anti-tumor activity against MDA-MB-231, HepG-2, and HGC-27 cells in vitro. The incorporation of MT effectively promoted the anti-tumor effect of BH, while the controlled release from liposomes further enhanced the therapeutic efficacy of BH. Furthermore, based on the flow cytometry results, we speculated that BH-MT-LP might promote apoptosis by blocking the G1 phase of cells and inducing cell death. In conclusion, BH-MT-LP provides evidence for the combined use of natural compounds as a stable, safe, and practical drug delivery system for the treatment of potential cancers. Meanwhile, the successful preparation for BH-MT-LP also provides a new approach to the combined use of traditional Chinese medicine ingredients. [ABSTRACT FROM AUTHOR]

Chitosan (Ch), a natural polysaccharide, is known for its biocompatibility, biodegradability, and various beneficial properties, including antioxidant and antibacterial activities. The objective of this study is to investigate the functionalization of zinc oxide (ZnO) with chitosan to develop a novel ZnO@Ch adduct for use in cosmetic formulations, specifically as a sun protection agent. The functionalization was achieved through ionotropic gelation, which enhanced the stability and reduced the photocatalytic activity of ZnO, thereby improving its safety profile for skin applications. FTIR spectroscopy confirmed the successful functionalization, while TGA and DSC characterized the thermal properties and stability. The Zeta potential and particle size analyses demonstrated improved stability of ZnO@Ch across various pH levels compared to uncoated ZnO. The structure of the obtained adduct was also confirmed by SEM analysis. The ZnO@Ch adduct exhibited enhanced stability at neutral and slightly alkaline pH values, reduced photocatalytic activity compared to pure ZnO, and had lower cytotoxicity in 3T3 cells compared to pure ZnO, particularly at higher concentrations. The ZnO@Ch adduct provided a higher Sun Protection Factor (SPF) and UVA Protection Factor (UVA-PF) than pure ZnO, indicating enhanced UV protection. The adduct's ability to provide higher SPF at lower ZnO concentrations offers economic and environmental benefits, aligning with sustainable product design principles. Future studies will focus on optimizing the formulation and testing the efficacy and safety at higher concentrations to fully realize its potential as a natural, eco-friendly sunscreen ingredient. [ABSTRACT FROM AUTHOR]

The biosynthesis of silver nanoparticles (AgNPs) presents an innovative and sustainable approach in nanotechnology with promising applications in fields such as medicine, food safety, and pharmacology. In this study, AgNPs were successfully synthesized using the probiotic strain Lacticaseibacillus rhamnosus (BCRC16000), addressing challenges related to stability, biocompatibility, and scalability that are common in conventional nanoparticle production methods. The formation of AgNPs was indicated by a color change from yellow to brown, and UV–visible spectrophotometry confirmed their presence with a characteristic absorption peak at 443 nm. Furthermore, Fourier transform infrared (FTIR) spectroscopy revealed the involvement of biomolecules in reducing silver ions, which suggests their role in stabilizing the nanoparticles. In addition, field emission scanning electron microscopy (FE-SEM) showed significant morphological and structural changes. At the same time, dynamic light scattering (DLS) and zeta potential analyses provided valuable insights such as average size (199.7 nm), distribution, and stability, reporting a polydispersity index of 0.239 and a surface charge of −36.3 mV. Notably, the AgNPs demonstrated strong antibacterial activity and photocatalytic efficiency, underscoring their potential for environmental and biomedical applications. Therefore, this study highlights the effectiveness of Lacticaseibacillus rhamnosus in the biosynthesis of AgNPs, offering valuable antibacterial and photocatalytic properties with significant industrial and scientific implications. [ABSTRACT FROM AUTHOR]