Efficacy Of Iron Oxide Nanoparticles Research Articles

Evaluation of antibacterial efficacy of iron oxide nanoparticles against Vibrio vulnificus: A comparative study with standard antibiotics

The synthesis and utilization of Fe2O3 nanoparticles are increasing due to their low cost, environmentally friendly, and biocompatible nature. Antimicrobial resistance is noticed as a global health concern by the community. Multidrug therapy and improper treatment of any disease cause an exponential increase in resistant microbial species. Therefore, improving the treatment schemes for curing different types of contagious ailments caused by microbes is essential. An economical co-precipitation technique was utilized for the preparation of Fe2O3 nanoparticles. The Fe2O3 nanostructures were analyzed by FTIR, ultraviolet–visible spectroscopy, XRD, and TEM techniques. The Fe2O3 nanoparticle's dimensions were determined to be 28.72 nm. A toxicity study of these Fe2O3 nanoparticles was carried out against a Gram-negative bacterium Vibrio vulnificus and showed toxic properties towards the Vibrio vulnificus. The antibacterial properties of these Fe2O3 nanoparticles were contrasted with commonly used antibiotics, including chloramphenicol, streptomycin, ampicillin, penicillin, Tetracycline, sulphatriad, Co-Trimoxazole, Clindamycin, Oxacillin, Erythromycin, and Chloramphenicol, etc., and found to be comparable in some cases even better antibacterial activity.

Enhanced Biocompatibility by Evaluating the Cytotoxic and Genotoxic Effects of Magnetic Iron Oxide Nanoparticles and Chitosan on Hepatocellular Carcinoma Cells (HCC)

Hepatocellular carcinoma (HCC), the fifth most prevalent cancer worldwide, is influenced by a myriad of clinic-pathological factors, including viral infections and genetic abnormalities. This study delineates the synthesis, characterization, and the biological efficacy of iron oxide nanoparticles (Fe3O4) and chitosan-coated iron oxide nanoparticles (Fe3O4-CS) against HCC. Analytical methods confirmed the successful synthesis of both nanoparticles, with Fe3O4-CS demonstrating a smaller, uniform spherical morphology and distinct surface and magnetic properties attributable to its chitosan coating. The prepared materials were analyzed using various techniques, and their potential cytotoxic effects on HepG2 cancer cells line for HCC were investigated. In biological evaluations against HepG2 cells, a notable distinction in cytotoxicity was observed. Fe3O4 showed modest anticancer activity with an IC50 of 383.71 ± 23.9 µg/mL, whereas Fe3O4 exhibited a significantly enhanced cytotoxic effect, with a much lower IC50 of 39.15 ± 39.2 µg/mL. The Comet assay further evidenced Fe3O4-CS potent DNA damaging effect, showcasing its superior ability to induce apoptosis through extensive DNA fragmentation. Biochemical analyses integrated into our results reveal that Fe3O4-CS not only induces significant DNA damage but also markedly alters oxidative stress markers. Compared to control and Fe3O4-treated cells, Fe3O4-CS exposure significantly elevated levels of oxidative stress markers: superoxide dismutase (SOD) increased to 192.07 U/ml, catalase (CAT) decreased to 0.03 U/L, glutathione peroxidase (GPx) rose dramatically to 18.76 U/gT, and malondialdehyde (MDA) levels heightened to 30.33 nmol/gT. These results underscore the potential of Fe3O4-CS nanoparticles not only in inducing significant DNA damage conducive to cancer cell apoptosis but also in altering enzymatic activities and oxidative stress markers, suggesting a dual mechanism of action that may underpin their therapeutic advantage in cancer treatment. Our findings advocate for the further exploration of Fe3O4-CS nanoparticles in the development of anticancer drugs, emphasizing their capability to trigger oxidative stress and enhance antioxidant defense mechanisms.

Glucosylation endows nanoparticles with TLR4 agonist capability to trigger macrophage polarization and augment antitumor immunity

Carbohydrates have emerged as promising candidates for immunomodulation, however, how to present them to immune cells and achieve potent immunostimulatory efficacy remains challenging. Here, we proposed and established an effective way of designing unique glyconanoparticles that can amplify macrophage-mediated immune responses through structural mimicry and multiple stimulation. We demonstrate that surface modification with glucose can greatly augment the immunostimulatory efficacy of nanoparticles, comparing to mannose and galactose. In vitro studies show that glucosylation improved the pro-inflammatory efficacy of iron oxide nanoparticles (IONPs) by up to 300-fold, with the immunostimulatory activity of glucosylated IONPs even surpassing that of LPS under certain conditions. In vivo investigation show that glucosylated IONPs elicited increased antitumor immunity and achieved favorable therapeutic outcomes in multiple murine tumor models. Mechanistically, we proposed that glucosylation potentiated the immunostimulatory effect of IONPs by amplifying toll-like receptors 4 (TLR4) activation. Specifically, glucosylated IONPs directly interacted with the TLR4-MD2 complex, resulting in M1 macrophage polarization and enhanced antitumor immunity via activation of NF-κB, MAPK, and STAT1 signaling pathways. Our work provides a simple modification strategy to endow nanoparticles with potent TLR4 agonist effects, which may shed new light on the development of artificial immune modulators for cancer immunotherapy.

Bacteria-Mediated Synthesis of Iron Oxide Nanoparticles and Their Efficiency in Ammonia Removal from Fish Culture Tanks

Background: Aquaculture is one of the most rapidly expanding food production sectors. Due to intensification, declining water quality parameters negatively impact fish production and the surrounding environment. Thus, it is essential to maintain optimum water quality parameters and aquatic ecosystems for sustainable fish production. This study aims to synthesize nanoparticles (NPs) and evaluate their efficiency against ammonia in cultured fish tanks under diverse conditions. Methods: Bacillus megaterium from the soil sample was isolated and identified. Iron oxide NPs were synthesized using Bacillus megaterium collected from soil samples and characterized by DLS-zeta potential, UV-vis, XRD, FTIR, and TEM analysis. Next, synthesized NPs were evaluated under ex-situ and in-situ conditions to determine their efficacy in removing ammonia from Common carp, Cyprinus carpio culture tanks. Results: B. megaterium was isolated, identified, and 16S rRNA gene PCR-amplified sequences confirm the identification of B megaterium. DLS-zeta potential, UV-vis, XRD, FTIR, and TEM analysis revealed the quality of synthesized NPs. B. megaterium from the soil sample was isolated and identified. The mean zeta potential of the biosynthesized NPs was between -4.65 to -6.45 mV and had an average size of 5 nm. The concentration of ammonia in aerated tanks treated with iron NPs reduced to less than 0.03 mg/dL from 0.3 mg/L. Also, fish mortality in these tanks was significantly controlled with the application of NPs. The application of NPs considerably reduced fish mortality in these fish tanks. Iron oxide NPs from B. megaterium can produce high-quality NPs that are efficient in removing ammonia from fish culture tanks. Further, exploratory studies are necessary to determine the efficacy of iron oxide NPs on aquatic organisms cultured in different environments.

Green synthesis and characterization of Fe3O4 nanoparticles using Chlorella-K01 extract for potential enhancement of plant growth stimulating and antifungal activity

The purpose of this research was to determine the efficacy of iron oxide nanoparticles (Fe3O4-NPs) using microalgal products as a plant growth stimulant and antifungal agent. The work was conducted with the phyco-synthesis and characterization of Fe3O4-NPs using 0.1 M ferric/ferrous chloride solution (2:1 ratio; 65 °C) with aqueous extract of the green microalga Chlorella K01. Protein, carbohydrate and polyphenol contents of Chlorella K01 extract were measured. The synthesized microalgal Fe3O4-NPs made a significant contribution to the germination and vigor index of rice, maize, mustard, green grams, and watermelons. Fe3O4-NPs also exhibited antifungal activity against Fusarium oxysporum, Fusarium tricinctum, Fusarium maniliforme, Rhizoctonia solani, and Phythium sp. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) scanning electron microscopy (SEM), transmission electron microscopy (TEM), particle size analysers (PSA), and zeta potential (ZP) measurements were used to characterize these green fabricated magnetite NPs. FTIR analysis showed that the synergy of microalgal proteins, carbohydrtates and polyphenols is responsible for the biofabrication of iron nanoparticles. A spheroid dispersion of biosynthesized Fe3O4-NPs with an average diameter of 76.5 nm was produced in the synthetic process.

Efficacy of Iron Oxide Nanoparticles in Diagnosis of Schistosomiasis

ABSTRACT Background: One of the worldwide major public health problems is urinary schistosomiasis that is caused by Schistosoma heamatobium. There are several immunodiagnostic methods used for that diagnosis of such disease, but some are more sensitive and specific than others. The tegumental Schistosoma-specific protein detection in serum samples is found out to be more valuable in diagnosis. Aim of the Work: To evaluate the efficacy of iron oxide nanoparticle for diagnosis of human schistosomiasis infections and to compare between ELISA-based iron oxide nanoparticle and traditional sandwich ELISA. Material and Methods: The tegumental antigen was purified from whole worms by DEAE-Sephadex G-75 ion-exchange chromatography and then was injected into rabbits to produce specific polyclonal antibodies (p Ab) which were then used as a primary capture in the indirect ELISA technique to reveal its reactivity using infected human sera. The anti- tegumental p Ab was then labeled with horse-radish peroxidase (HRP) and used as a secondary capture. Sandwich ELISA was done for serum samples of humans and hamsters infected with S. haematobium. Results: The sensitivity of the traditional sandwich ELISA with anti-tegumental p Ab was 85% and it increased by using the sandwich IMB-ELISA to be 95% in serum. The specificity of sandwich ELISA was 88.2% and it increased by using the sandwich IMB-ELISA to be 92.6%. Conclusion: The data obtained concluded that the IMB-ELISA appears to be a sufficiently sensitive and feasible assay for the detection of schistosomal antigenemia and the evaluation of its potential use in human schistosomiasis is in progress. Keywords: S. haematobium; diagnosis; ELISA; Immunomagnetic bead ELISA technique; Paramagnetic nanoparticles.

The Effect of Cage Shape on Nanoparticle-Based Drug Carriers: Anticancer Drug Release and Efficacy via Receptor Blockade Using Dextran-Coated Iron Oxide Nanocages.

Although a range of nanoparticles have been developed as drug delivery systems in cancer therapeutics, this approach faces several important challenges concerning nanocarrier circulation, clearance, and penetration. The impact of reducing nanoparticle size on penetration through leaky blood vessels around tumor microenvironments via enhanced permeability and retention (EPR) effect has been extensively examined. Recent research has also investigated the effect of nanoparticle shape on circulation and target binding affinity. However, how nanoparticle shape affects drug release and therapeutic efficacy has not been previously explored. Here, we compared the drug release and efficacy of iron oxide nanoparticles possessing either a cage shape (IO-NCage) or a solid spherical shape (IO-NSP). Riluzole cytotoxicity against metastatic cancer cells was enhanced 3-fold with IO-NCage. The shape of nanoparticles (or nanocages) affected the drug release point and cellular internalization, which in turn influenced drug efficacy. Our study provides evidence that the shape of iron oxide nanoparticles has a significant impact on drug release and efficacy.

<i>Balanites aegyptiaca</i> Oil Synthesized Iron Oxide Nanoparticles: Characterization and Antibacterial Activity

Antibacterial activity of iron oxide nanoparticles, an employing B. aegyptiaca oil (L.) Del., was used as natural stabilizer by modifying a co-precipitation method. In this work, we chose B. aegyptiaca oil as the new surfactant coating agent, and synthesized B. aegyptiaca oil coating with iron oxide nanoparticles which were characterized with a variety of methods, including Gas Chromatography (GC) to determine the fatty acids composition of the seeds oil, Fourier Transform-Infrared Spectroscopy (FTIR), Transmission Electron Microscopy (TEM) equipped with Energy Dispersive Spectroscopy (EDS), X-ray Powder Diffractometer (XRD) and Vibrating Sample Magnetometer (VSM). In antibacterial studies, disk diffusion susceptibility test was used to measure efficacy of iron oxide nanoparticles against Gram-positive bacteria Staphylococcus aureus (S. aureus), Bacillus subtilis (B. subtilis) and Gram-negative bacteria Escherichia coli (E. coli) in terms of zone inhibition. The B. aegyptiaca coated on the surface of iron oxide nanoparticles; its particle size was found to be nanoscale below 50 nm, and the magnetization (δs) was 16.975 emu g-1. Antibacterial activity was measured. Efficacy of iron oxide nanoparticles against bacterial strains was found in Escherichia coli (E. coli). All these findings suggest that the nanoparticles synthesized from B. aegyptiaca oil may be a promising reagent for a wide variety of applications in biological fields as well as in nanomedicine.