Synergistic antifungal activity of lepidium sativum ZnO nanoparticles and nystatin against resistant candida species

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The rising threat of drug-resistant fungal pathogens such as Candida albicans poses a particular risk to disability patients, who often face heightened vulnerability to infections due to compromised immune function and frequent medical interventions, demanding innovative therapeutic approaches. This study presents a green synthesis of zinc oxide nanoparticles (ZnO-NPs) using Lepidium sativum seed extract as a promising strategy. The resulting ZnO-NPs were Characterized as crystalline with a hexagonal wurtzite structure and an average size of 32 nm. They demonstrated significant multifunctional biological activities, exhibiting potent, dose-dependent antifungal activity against Candida albicans and Candida tropicalis, with minimum inhibitory concentrations (MICs) of 125 µg/mL and 62.5 µg/mL, respectively. A key finding was the strong synergistic effect observed when ZnO-NPs were combined with nystatin, which showed an increase in fold area (IFA) of 0.85 and 0.99 against C. albicans and C. tropicalis, respectively. This synergistic interaction was further quantitatively confirmed by fractional inhibitory concentration index (FICI) values of 0.38 and 0.25 for the respective species. Furthermore, the ZnO-NPs displayed considerable antioxidant capacity (IC₅₀: 335.48 µg/mL) and promising selective cytotoxicity, demonstrating significantly greater potency against hepatoma (HUH7) cells (IC₅₀: 145.2 µg/mL) than against normal lung fibroblasts (WI38) (IC₅₀: 237.6 µg/mL). These results underscore the potential of L. sativum-derived ZnO-NPs as effective antifungal agents, particularly as adjuvants to enhance the efficacy of existing drugs like nystatin, while also offering antioxidant activity and favorable biocompatibility. This study advocates for further investigation into their mechanisms of action and in vivo efficacy to advance clinical applications.

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This study provides evidence for the green synthesis of zinc oxide nanoparticles (ZnO NPs) using Vitex negundo leaf extract. The UV–Visible (UV–Vis) spectrum of ZnO NPs and calcinated ZnO NPs (ZnO-C) showed peaks at 370[Formula: see text]nm and 374[Formula: see text]nm, respectively, confirming zinc ion reduction to zinc oxide. The ZnO NPs and calcinated counterparts were further characterized by FTIR, XRD, FE-SEM and EDX. FTIR results revealed the presence of alcoholic and aromatic groups, like flavonoids, in the leaf extract. The XRD pattern showed a distinctive Wurtzite crystalline phase with a hexagonal shape. The Brunauer–Emmett–Teller (BET) analysis data revealed that ZnO’s surface area and pore size is 22.8[Formula: see text]m2/g and 12.9[Formula: see text]nm, whereas ZnO-C exhibited a surface area of 23.5[Formula: see text]m2/g and pore size of 13.1[Formula: see text]nm. The SEM data demonstrated numerous irregular and agglomerated flakes fusing to form a roughly spherical morphology with the size, in the range of 15–20[Formula: see text]nm and 11–16[Formula: see text]nm for ZnO and ZnO-C NPs, respectively. The results of the antimicrobial assay by disc diffusion method and MIC testing revealed that ZnO and ZnO-C NPs exhibited moderate to high antimicrobial activity against various microorganisms, indicating their application against bacterial infection. In addition, the ZnO NPs significantly disrupted the biofilm of Bacillus cereus and Pseudomonas aeruginosa, as confirmed by CV assay and fluorescent microscopy.

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In this work, we report a green synthesis of zinc oxide (ZnO) nanoparticles using aqueous and ethanolic extracts of Tradescantia spathacea (purple maguey) as bioreducing and stabilizing agents, which are plant extracts not previously employed for metal oxide nanoparticle synthesis. This method provides an efficient, eco-friendly, and reproducible route to obtain ZnO nanoparticles, while minimizing environmental impact compared to conventional chemical approaches. The extracts were prepared following a standardized protocol, and their phytochemical profiles, including total phenolics, flavonoids, and antioxidant capacity, were quantified via UV-Vis spectroscopy to confirm their reducing potential. ZnO nanoparticles were synthesized using zinc acetate dihydrate as a precursor, with variations in pH and precursor concentration in both aqueous and ethanolic media. UV-Vis spectroscopy confirmed nanoparticle formation, while X-ray diffraction (XRD) revealed a hexagonal wurtzite structure with preferential (101) orientation and lattice parameters a = b = 3.244 Å, c = 5.197 Å. Scanning electron microscopy (SEM) showed agglomerated morphologies, and Fourier transform infrared spectroscopy (FTIR) confirmed the presence of phytochemicals such as quercetin, kaempferol, saponins, and terpenes, along with Zn–O bonding, indicating surface functionalization. Zeta potential measurements showed improved dispersion under alkaline conditions, particularly with ethanolic extracts. This study presents a sustainable synthesis strategy with tunable parameters, highlighting the critical influence of precursor concentration and solvent environment on ZnO nanoparticle formation. Notably, aqueous extracts promote ZnO synthesis at low precursor concentrations, while alkaline conditions are essential when using ethanolic extracts. Compared to other green synthesis methods, this strategy offers control and reproducibility and employs a non-toxic, underexplored plant source rich in phytochemicals, potentially enhancing the crystallinity, surface functionality, and application potential of the resulting ZnO nanoparticles. These materials show promise for applications in photocatalysis, in antimicrobial coatings, in UV-blocking formulations, and as functional additives in optoelectronic and environmental remediation technologies.

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Synthesis of zinc oxide nanoparticles using tea leaf extract and its application for solar cell
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We report the synthesis of zinc oxide (ZnO) nanoparticles and its composite with natural graphite (NG) powder for application in solar cell. ZnO nanoparticles were synthesized using green tea leaf extract as non-toxic and eco-friendly reducing material under microwave irradiation. The formation of ZnO nanoparticles was monitored by the colour changes during the reaction. The synthesized ZnO nanoparticles were characterized by particle size analyzer (dynamic light scattering), scanning electron microscope, UV–visible spectroscopy, atomic force microscope and fluorescence spectroscopy. The average particle size of the ZnO nanoparticles was found to be 26 nm. The synthesized ZnO nanoparticles were further used to prepare ZnO/NG composite material with commercially available NG powder. The current–voltage (I–V) characteristics of thin film of ZnO/NG nanocomposite were investigated. J SC (short-circuit photocurrent), V OC (open-circuit photovoltage), FF (fill factor) and η (efficiency of the solar cell) were measured for ZnO/NG nanocomposite. Interestingly, the cell showed a good power conversion efficiency of 3.54% with high stability.

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Various eco-friendly techniques are being researched for synthesizing ZnO-NPs, known for their bioactivity. This study aimed at biosynthesizing ZnO-NPs using Streptomyces baarnensis MH-133, characterizing their physicochemical properties, investigating antibacterial activity, and enhancement of their efficacy by combining them with a water-insoluble active compound (Ka) in a nanoemulsion form. Ka is a pure compound of 9-Ethyl-1,4,6,9,10-pentahydroxy-7,8,9,10-tetrahydrotetracene-5,12-dione obtained previously from our strain of Streptomyces baarnensis MH-133. Biosynthesized ZnO-NPs employing Streptomyces baarnensis MH-133 filtrate and zinc sulfate (ZnSO4.7H2O) as a precursor were purified and characterized by physicochemical investigation. High-resolution-transmission electron microscopy (HR-TEM) verified the effective biosynthesis of ZnO-NPs (size < 12 nm), whereas dynamic light scattering (DLS) analysis showed an average size of 17.5 nm. X-ray diffraction (XRD) exhibited characteristic diffraction patterns that confirmed crystalline structure. ZnO-NPs efficiently inhibited both Gram-positive and Gram-negative bacteria (MICs: 31.25–125 µg/ml). The pure compound (Ka) was combined with ZnO-NPs to improve effectiveness and reduce dose using checkerboard microdilution. Niteen treatments of Ka and ZnO-NPs combinations obtained by checkerboard matrix inhibited Klebsiella pneumonia. Eleven combinations had fractional inhibitory concentration index (FICi) between 1.03 and 2, meaning indifferent, another five combinations resulted from additive FICi (0.625–1) and only one combination with FICi of 0.5, indicating synergy. In the case of methicillin-resistant S. aureus (MRSA), Ka-ZnO-NPs combinations yielded 23 treatments with varying degrees of interaction. The results showed eleven treatments with indifferent interaction, eight additive interactions, and two synergies with FICi of 0.5 and 0.375. The combinations that exhibited synergy action were transformed into a nanoemulsion form to improve their solubility and bioavailability. The HR-TEM analysis of the nanoemulsion revealed spherical oil particles with a granulated core smaller than 200 nm and no signs of aggregation. Effective dispersion was confirmed by DLS analysis which indicated that Ka-ZnO-NPs nanoemulsion droplets have an average size of 53.1 nm and a polydispersity index (PI) of 0.523. The killing kinetic assay assessed the viability of methicillin-resistant Staphylococcus aureus (MRSA) and K. pneumonia post-treatment with Ka-ZnO-NPs combinations either in non-formulated or nanoemulsion form. Results showed Ka-ZnO-NPs combinations show concentration and time-dependent manner, with higher efficacy in nanoemulsion form. The findings indicated that Ka-ZnO-NPs without formulation at MIC values killed K. pneumonia after 24 h but not MRSA. Our nanoemulsion loaded with the previously mentioned combinations at MIC value showed bactericidal effect at MIC concentration of Ka-ZnO-NPs combination after 12 and 18 h of incubation against MRSA and K. pneumonia, respectively, compared to free combinations. At half MIC value, nanoemulsion increased the activity of the combinations to cause a bacteriostatic effect on MRSA and K. pneumonia after 24 h of incubation. The free combination showed a bacteriostatic impact for 6 h before the bacteria regrew to increase log10 colony forming unit (CFU)/ml over the initial level. Similarly, the cytotoxicity study revealed that the combination in nanoemulsion form decreased the cytotoxicity against kidney epithelial cells of the African green monkey (VERO) cell line. The IC50 for Ka-ZnO-NPs non-formulated treatment was 8.17/1.69 (µg/µg)/ml, but in nano-emulsion, it was 22.94 + 4.77 (µg/µg)/mL. In conclusion, efficient Ka-ZnO-NPs nanoemulsion may be a promising solution for the fighting of ESKAPE pathogenic bacteria according to antibacterial activity and low toxicity.

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Synthesis of ZnO nanoparticles from zinc acetate dihydrate – An environmental friendly technique
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Facile synthesis and characterization of zinc oxide nanoparticles and studies of their catalytic activity towards ultrasound-assisted degradation of metronidazole
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