Synthesis Of Iron Oxide Nanoparticles Research Articles

Synthesis and characterisation of iron oxide nanoparticles with thymoquinone

Synthesis and characterisation of iron oxide nanoparticles with thymoquinone

Low-cost one-pot synthesis of hydrophobic and hydrophilic monodispersed iron oxide nanoparticles

A one-pot synthesis of monodispersed iron oxide nanoparticles starting with iron nitrate and control of morphology, dimension and dispersibility.

Assessment of the neuroprotective effect of green synthesized iron oxide nanoparticles capped with curcumin against a rat model of Parkinson's disease.

The current study aims to investigate the protective effect of iron oxide nanoparticles capped with curcumin (FeONPs-Cur) against motor impairment and neurochemical changes in a rat model of Parkinson's disease (PD) induced by reserpine. Rats were grouped into control, PD model induced by reserpine, and PD model treated with FeONPs-Cur (8 rats/group). The open field test was used to assess motor activity. The concentration of dopamine (DA), norepinephrine (NE), serotonin (5-HT), lipid peroxidation (MDA), reduced glutathione (GSH), and nitric oxide (NO), and the activities of Na+,K+,ATPase, acetylcholinesterase (AchE), and monoamine oxidase (MAO) were determined in the midbrain and striatum. Data were analyzed by ANOVA at P-value<0.05. The PD model exhibited a decrease in motor activity. In the midbrain and striatum of the PD model, DA, NE, and 5-HT levels decreased significantly (P-value<0.05). However, an increase in MAO, NO, and MDA was observed. GSH, AchE and Na+,K+,ATPase decreased significantly in the two brain areas. FeONPs-Cur prevented the decline of dopamine and norepinephrine and reduced oxidative stress in both areas. It also prevented the increased MAO activity in the two areas and the inhibited activity of AchE and Na+,K+,ATPase in the midbrain. These changes were associated with improvements in motor activity. The present data indicate that FeONPs-Cur could prevent the motor deficits induced in the PD rat model by restoring dopamine and norepinephrine in the midbrain and striatum. The antioxidant activity of FeONPs-Cur contributed to its protective effect. These effects nominate FeONPs-Cur as an antiparkinsonian candidate.

Review—Potential of Tunneling Magnetoresistance Coupled to Iron Oxide Nanoparticles as a Novel Transducer for Biosensors-on-Chip

Biosensors-on-chip (BoC), compact and affordable public diagnostic devices, are vital for preventing health crises caused by viral and bacterial mutations, climate change, and poor diets. Clinical, remote, and field use are possible with these devices. BoC is used in food safety, environmental monitoring, and medical diagnosis. The coupling of tunneling magnetoresistance (TMR) sensing elements in chip form with surface functionalized iron oxide nanoparticles (IONPs) as a biomarker, known as TMR/ IONPs, allows BoC devices to be made. The functional framework of BoC based on TMR/ IONPs, the instrument system, and biomolecule immobilization will be covered in this review. This review aims to overview the recent research on a biosensor using TMR technology with IONPs biomarkers and discuss its future advances in point-of-care diagnostics. TMR sensors have revolutionized low-magnetic field sensing technologies, yet biosensing faces challenges. However, it’s important to recognize that TMR sensors exclusively utilize out-of-plane connections. that creates a larger separation between biomolecules and the sensing layer, leading to a decrease in the sensitivity of biomolecules. Large magnetization of dispersed IONPs to generate sufficient stray-field, compact and inexpensive instrumentation to sense the low voltage yielded by the TMR/IONPs system, and high-selectivity bio-analyte immobilization to the surface of IONPs to increase sensor sensitivity are the notable issues to address this problem. The utilization of the green synthesized method in producing IONPs for magnetic labeling can enhance the sensitivity of a TMR-based biosensor. This is achieved through the formation of IONPs with a capping agent on its surface that inhibits the aggregation and facilitates the immobilization of the biomolecule target. Additionally, improving device performance requires creating high-TMR materials. Despite challenges, research and technological advances hold great promise for TMR/GS-IONP bio-applications.

Hybrid polyionic complexes as nanoreactors for the synthesis of iron oxide nanoparticles: From size control to modulation of magnetic and catalytic properties

Hybrid polyion complexes (HPICs) obtained from the complexation in aqueous solution of a double hydrophilic block copolymers and metal ions can act as efficient precursors for the controlled synthesis of hybrid nanoparticles. Hence, HPICs based on a mixture of ferrous and ferric ions with poly(ethylene oxide)-block-poly(acrylic acid) were used to initiate, after the addition at 70 °C of a solution of NH4OH, the formation of iron oxide nanoparticles. The careful choice of the molar ratio between polymer and metal ions within HPICs enables to tune the morphology and size of the obtained iron oxide nanoparticles while maintaining the same surface composition. This control of size and composition was further used to highlight the relationship between the size of these particles and their catalytic and magnetic properties.

Characterization and Antibacterial Potential of Iron Oxide Nanoparticles in Eradicating Uropathogenic E. coli.

Proper management and control measurements are needed to stop the spread of highly pathogenic E. coli isolates that cause urinary tract infections (UTI) by developing new antibacterial agents to ensure the safety of public health. Therefore, the present investigations were used to achieve the synthesis of iron oxide nanoparticles (IONPs) via a simple coprecipitation method using ferric nitrates Fe (NO3)3 as the precursor and hydrazine solution as the precipitator and to explore the antibacterial activity against eradicating Uropathogenic Escherichia coli (E. coli). The synthesized IONPs were further studied using a UV-vis spectrophotometer, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and scanning electron microscopic (SEM) analysis. The maximum surface plasmon resonance peak was observed as absorption at 320 nm in a colloidal solution to validate the synthesis of IONPs. The FT-IR analysis was used to identify different photoactive functional groups that were responsible for the reduction of Fe (NO3)3 to IONPs. The crystalline nature of synthesized IONPs was revealed by XRD patterns with an average particle size ranging as 29 nm. The SEM image was employed to recognize the irregular morphology of synthesized nanoparticles. Moreover, significant antibacterial activity was observed at 1 mg/mL stock solution but after (125, 250, and 500 μg/mL) dilution, the synthesized IONPs showed moderate activity and became inactive at lower concentrations. The morphological and biochemical tests were used to confirm the presence of E. coli in the samples. Furthermore, the minimum inhibitory concentration (MIC) and minimum bacterial concentration (MBC) were carried out to determine the inhibitory concentrations for the isolated bacteria. The isolated E. coli were also subjected to antibiotic sensitivity testing that showed high resistance to antibiotics such as penicillin and amoxicillin. Thus, the findings of this study were to use IONPs against antibiotic resistance that has been developed in an inappropriate way.

Synthesis of Plant-Mediated Iron Oxide Nanoparticles and Optimization of Chemically Modified Activated Carbon Adsorbents for Removal of As, Pb, and Cd Ions from Wastewater.

This research study was designed with the aim to prepare plant extract-mediated iron oxide nanoparticles (IONPs) and different chemically modified carbon adsorbents from the Parthenium hysterophorus plant and then optimize the carbon adsorbents by evaluating their adsorption applications in wastewater for the selected metal ions like arsenic (As3+), lead (Pb2+), and cadmium (Cd2+). The Fourier transform infrared spectroscopy (FTIR) technique was used to highlight functional groups in plant-mediated IONPs and chemically modified carbon adsorbents. A scanning electron microscopy study was conducted to explain the surface morphology of the adsorbents. Energy-dispersive X-rays was used for elemental analysis and X-ray diffraction for particle size and crystallinity of the adsorbents. From the study, it was found that the best optimum conditions were pH = 5-6, initial concentration of adsorbate of 10 mg/L, dose of adsorbent of 0.01 g, contact time of 90-120 min of adsorbent and adsorbate, and temperature of 25 °C. At optimum conditions, the adsorption capacities of IONPs for arsenic (As) 144.7 mg/g, lead (Pb) 128.01 mg/g, and cadmium (Cd) ions 122.1 mg/g were recorded. The activated carbon at optimum conditions showed adsorption capacities of 46.35 mg/g for As, 121.95 mg/g for Pb, and 113.25 mg/g for Cd ion. At equilibrium, Langmuir, Freundlich Temkin, and Dubinin-Radushkevich isotherms were applied on the experimental adsorption data having the best R2 values (0.973-0.999) by the Langmuir isotherm. High-correlation coefficient R2 values (0.996-0.999) were obtained from the pseudo-second-order for all cases, showing that the adsorption process proceeds through pseudo second-order kinetics. The apparent adsorption energy E value was in the range of 0.24-2.36 kJ/mol. The adsorption capacity of regenerated IONPs for As gradually decreased from 144.8 to 45.67 mg/g, for lead 128.15 to 41.65 mg/g, and cadmium from 122.10 to 31.20 mg/g in 5 consecutive cycles. The study showed that the synthesized IONPs and acid-activated carbon adsorbent were successfully used to remove selected metal ions from wastewater.

Synthesis of superparamagnetic iron oxide nanoparticles coated with polyethylene glycol as potential drug carriers for cancer treatment

Current cancer treatments are not selective in delivering drugs to cancer cells, affecting healthy tissues and especially rapidly dividing cells. This work describes the development of superparamagnetic nanoparticles for drug delivery through green synthesis, mediated by Musa paradisiaca peel extract as a stabilizing and reducing agent. The nanoparticles’ structural, morphological, magnetic and chemical properties were evaluated. The XRDs showed a cubic crystal structure with the space group of Fd3m (No. 227), typical of magnetite. Through SEM and TEM, it was determined that the mean size of the nanoparticles was 11.61 nm. FTIR and EDS confirmed the successful synthesis of Fe3O4 nuclei, covered with polyethylene glycol and loaded with doxorubicin. The magnetic properties of the nanocomposites obtained were measured using VSM, evidencing a superparamagnetic behaviour with a Ms = 72.75 emu/g. Finally, MTT assays on the HeLa tumour line showed a 45.5% decrease in cell viability. The determined properties allow the application of the nanocomposite produced as a potential candidate for cancer treatment.Graphical

Synthesis of iron oxide nanoparticles encapsulated poly(styrene‐co‐4‐vinyl pyridine) nanocomposites for column adsorption and photocatalytic degradation of para nitrophenol from water

AbstractStyrene (St), 1,4 vinyl pyridine (4VP) monomers and divinyl benzene (DVB) monomer‐cum‐crosslinker at different molar ratios were subjected to emulsion polymerization in the presence of FeCl2, 6H2O/FeCl3⋅4H2O followed by the treatment with an aqueous ammonia solution to produce several iron oxide nanoparticles (IONs) impregnated crosslinked copolymer composites. The resulting polymer metal nanocomposites (PMNCs) were characterized by FTIR, proton and 13C NMR, UV–visible spectroscopy, XRD, XPS, DLS, magnetic properties, SEM and TEM. The PMNCs were used for batch and column adsorption and photocatalytic degradation of p‐nitrophenol (PNP) from water. The PMNC4 composite prepared with an styrene:4VP molar ratio of 5:1 (16.7 mol% 4VP), 4 wt.% DVB crosslinker and 0.025/0.05 molar ratios of Fe(II)/Fe(III) salts leads to an optimum batch equilibrium adsorption (qe, mg/g)/removal% of 496.36/99.3 PNP from aqueous PNP of concentration 100 mg/L. The same composite showed an equilibrium PNP adsorption (qe) of 114.2 mg/g polymer and a removal% of 26.8 for an inlet feed concentration (Ci, mg/L)/flow rate (Qt, mL/min)/bed height (h, mm) of 100/30/30 in a fixed bed. The PMNC4 polymer showed a photodegradation efficiency of 98% with a 1st order rate constant of 0.029 min−1 after 70 min of degradation of 100 mg/L PNP in solar light.Highlights Copolymer network of styrene, 4 vinyl pyridine and DVB were synthesized. Iron oxide nanoparticles were introduced into the network in‐situ during synthesis. The metal polymer nanocomposites (PMNCs) were characterized. Synthesis parameters were optimized with respect to batch adsorption of PNP. PMNCs showed excellent fixed bed adsorption and photocatalytic degradation of PNP.

Biogenic synthesis of iron oxide nanoparticles and experimental modeling studies on the removal of heavy metals from wastewater

Water pollution is a major global challenge due to the fast expansion of industrial activities and the increasing human population. Certain heavy metals can be exceedingly hazardous and contribute significantly to water contamination. In this study, iron oxide nanoparticles (IONPs) were synthesized using cyanobacteria extract to remove heavy metals (Cd and Pb) from the wastewater. To characterize the IONPs, several analytical techniques were employed such as Ultraviolet–visible spectroscopy revealed a SPR (surface plasmon resonance) peak at 348 nm and FTIR (Fourier transform infrared) spectral analysis showed the OH, C–H and S=O functional groups which confirmed the biomolecules responsible for the biogenic synthesis and stability. The surface morphology of the biogenic IONPs was investigated using SEM (scanning electron microscopy) which reveled their nearly spherical or cubic shape. Additionally, XRD (X-ray diffraction) analysis confirmed the crystallinity of IONPs, with a crystalline size measuring 18.21 nm. Effects of contact time, pH, initial metal ions concentrations, and IONPs dosage were studied on the adsorption of Cd and Pb ions. Different adsorption kinetics and isotherm models were applied to the experimental data. Pseudo second-order kinetic and Langmuir isotherm models were well fitted to the adsorption of Cd and Pb onto the IONPs. Higher correlation coefficients (R2) values of Langmuir isotherm (R2: 0.990 for Cd and Pb adsorption) and Pseudo second-order kinetic (R2: 0.998 and 0.999 for Cd and Pb adsorption, respectively) were found, which indicated the favorable interaction between the metal ions and adsorbent. Langmuir isotherm calculated maximal adsorption capacities of 105.932 and 118.764 mg/g for Cd and Pb, respectively. Recyclability of IONPs was conducted and after five adsorption/desorption cycles, IONPs retained their adsorption efficiency with negligible decline. After five cycles, IONPs removal efficiency was up to 80.41 and 88.35 % for Cd and Pb, respectively. Results of this study indicate that cyanobacteria-mediated IONPs were efficient adsorbent for Pb and Cd removal from contaminated aqueous solution.

Plant Synthesized Iron Oxide Nanoparticles for Removal of Emerging Contaminant

Plant Synthesized Iron Oxide Nanoparticles for Removal of Emerging Contaminant

Modification of the Codeposition Method for the Synthesis of Iron-Oxide Nanoparticles with a High Magnetization Value and a Controlled Reaction Yield

Modification of the Codeposition Method for the Synthesis of Iron-Oxide Nanoparticles with a High Magnetization Value and a Controlled Reaction Yield

Green synthesis of iron oxide nanoparticles from Spermacoce ocymoides Burm.f. plant extracts for targeted lung cancer A549 cell therapy

The present study evaluated the synthesis of iron oxide nanoparticles using Spermacoce ocymoides Burm.f. plant extracts, and the effects of plant based iron oxide nanoparticles on A549 lung cancer cells were investigated to elucidate their impact on cellular morphology, mitochondrial function, and apoptotic pathways. Spermacoce ocymoides plant based iron oxide nanoparticles were characterised by X-ray diffraction, Atomic force microscopy, FTIR, and UV-Vis absorption spectroscopy. Iron oxide nanoparticle treatment caused considerable morphological alterations in A549 cells, including cell shrinkage, detachment, membrane blabbing, and distorted shape, consistent with cellular stress and potential apoptotic events. MMP analysis revealed a dose-dependent decrease in mitochondrial membrane potential, implying that nanoparticles have an effect on mitochondrial function. The presence of reactive oxygen species suggested that oxidative stress was involved in the cellular response to iron oxide nanoparticles. Additionally, DNA fragmentation analysis confirmed the activation of apoptotic pathways, with the nanoparticles themselves serving as a positive control for inducing apoptosis. The observed morphological changes, altered mitochondrial function, ROS production, and DNA fragmentation collectively point towards apoptotic cell death pathways being triggered by the nanoparticles.&#x0D; KEY WORDS: Spermacoce ocymoides, Iron oxide nanoparticles, A549 cells, Apoptotic&#x0D; Bull. Chem. Soc. Ethiop. 2024, 38(1), 123-134. DOI: https://dx.doi.org/10.4314/bcse.v38i1.10

Insights on the synthesis of iron-oxide nanoparticles and the detection of iron-reducing genes from soil microbes

This study explores the potential of some soil bacteria in the synthesis of iron oxide nanoparticles (IONPs), highlighting their advantages in terms of iron uptake and tolerance capacity. Soil samples collected from a metal fabricating workshop were successively screened in nutrient broth containing 1% iron salts (Fe2O3, FeCl3, and FeSO4) following a standard microbiological sampling technique. The recovered bacterial isolates (persister cells) were identified using polymerase chain reaction (PCR) and 16S rRNA sequencing. Ten bacterial isolates identified as Sporosarcina luteola, Bacillus badius (2), Bacillus subtilis (2), Bacillus tropicus, Bacillus cereus, Klebsiella pneumoniae, Klebsiella quasipneumoniae and Klebsiella africana were recovered. The method reports that six of the bacterial isolates extracellularly synthesize IONPs and the result from the energy dispersion x-ray (EDX) spectral analysis indicated varying weight percentages of bio-reduced iron by Bacillus subtilis-A12 (48.59%), Klebsiella quasipneumoniae (39.99%), Bacillus subtilis-B1 (39.97%), Bacillus cereus (38.62%), Bacillus badius (33.79%) and Klebsiella africana (32.61%). The IONPs exhibited absorbance peaks in the range of 250–350 nm, with a mean area size estimated between 31–72 nm using ImageJ software. Additionally, the presence of iron reductase (fhu) and cysteine desulfurase (suf) genes were detected in the recovered Bacillus and Klebsiella species through PCR analysis. This study has provided valuable insights into the physiology and genomic functions essential for microbial synthesis of IONPs and their relevance to nano-bioremediation.

Sal (Shorea robusta) seed deoiled cake-based synthesis of magnetic iron oxide nanoparticles for the decolorization of acid fuchsin dye: a sustainable cleaner environmental approach

Sal (Shorea robusta) seed deoiled cake-based synthesis of magnetic iron oxide nanoparticles for the decolorization of acid fuchsin dye: a sustainable cleaner environmental approach

Unveiling the effect of gibberellin-induced iron oxide nanoparticles on bud dormancy release in sweet cherry (Prunus avium L.)

Hydrogen cyanide has been extensively used worldwide for bud dormancy break in fruit trees, consequently enhancing fruit production via expedited cultivation, especially in areas with controlled environments or warmer regions. A novel and safety nanotechnology was developed since the hazard of hydrogen cyanide for the operators and environments, there is an urgent need for the development of novel and safety approaches to replace it to break bud dormancy for fruit trees. In current study, we have systematically explored the potential of iron oxide nanoparticles, specifically α-Fe2O3, to modulate bud dormancy in sweet cherry (Prunus avium). The synthesized iron oxide nanoparticles underwent meticulous characterization and assessment using various techniques, including Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and ultraviolet–visible infrared (UV–Vis) spectroscopy. Remarkably, when applied at a concentration of 10 mg L−1 alongside gibberellin (GA4+7), these iron oxide nanoparticles exhibited a substantial 57% enhancement in bud dormancy release compared to control groups, all achieved within a remarkably short time span of 4 days. Our RNA-seq analyses further unveiled that 2757 genes within the sweet cherry buds were significantly up-regulated when treated with 10 mg L−1 α-Fe2O3 nanoparticles in combination with GA, while 4748 genes related to dormancy regulation were downregulated in comparison to the control. Moreover, we discovered an array of 58 transcription factor families among the crucial differentially expressed genes (DEGs). Through hormonal quantification, we established that the increased bud burst was accompanied by a reduced concentration of abscisic acid (ABA) at 761.3 ng/g fresh weight in the iron oxide treatment group, coupled with higher levels of gibberellins (GAs) in comparison to the control. Comprehensive transcriptomic and metabolomic analyses unveiled significant alterations in hormone contents and gene expression during the bud dormancy-breaking process when α-Fe2O3 nanoparticles were combined with GA. In conclusion, our findings provide valuable insights into the intricate molecular mechanisms underlying the impact of iron oxide nanoparticles on achieving uniform bud dormancy break in sweet cherry trees.

Dextran coated iron oxide nanoparticles loaded with protocatechuic acid as multifunctional therapeutic agents

Nowadays, there is a growing interest in multifunctional therapeutic agents as valuable tools to improve and expand the applicability field of traditional bioactive compounds. In this context, the synthesis and main characteristics of dextran-coated iron oxide nanoparticles (IONP-Dex) loaded with both an antioxidant, protocatechuic acid (PCA), and an antibiotic, ceftazidime (CAZ) or levofloxacin (LEV) are herein reported for the first time, with emphasis on the potentiation effect of PCA on drugs activity. All nanoparticles were characterized by transmission electron microscopy, X-ray diffraction, vibrating sample magnetometry, differential scanning calorimetry and dynamic light scattering. As evidenced by DPPH method, IONP-Dex loaded with PCA and LEV had similar antioxidant activity like those with PCA only, but higher than PCA and CAZ loaded ones. A synergy of action between PCA and each antibiotic co-loaded on IONP-Dex has been highlighted by an enhanced activity against reference bacterial strains, such as S. aureus and E. coli after 40 min of incubation. It was concluded that PCA, which is the main cause of the antioxidative properties of loaded nanoparticles, further improves the antimicrobial activity of IONP-Dex nanoparticles when was co-loaded with CAZ or LEV antibiotics. All constructs also showed a good biocompatibility with normal human dermal fibroblasts.

Escherichia coli-assisted synthesis of AgFeO2 nanoparticles for antimicrobial, photocatalytic and hydrogen generation applications

The nanoparticles produced by physical and chemical methods are toxic in one or other way. Green chemistry is an emerging, stable and eco-friendly approach for biological production of nanomaterials. In the present study, Escherichia coli bacterium was utilized for the synthesis of silver iron oxide (AgFeO2) nanoparticles by using precursors of two different salts; iron nitrate (Fe(No3)3 and silver nitrate (AgNO3). Synthesized nanoparticles were characterized by EDX, XRD and SEM. AgFeO2 nanoparticles, members of delafossite family were appraised for bacterial inactivation, photocatalytic degradation of toxic dyes and hydrogen generation through methanolysis. Delafossites are chemically stable compounds with high conductivity and decomposition temperatures (800–925 °C). The antimicrobial activity of AgFeO2 nanoparticles was checked by well diffusion method against ATTC cultures of Escherichia coli, Bacillus subtilis, Staphylococcus aureus and Pseudomonas aeruginosa. Synthesized AgFeO2 nanoparticles were employed for the degradation of Cango red and maximum degradation of 87 % was accomplished with 20 ppm (50 mL) solution of Cango red and 0.10 g AgFeO2 as catalyst and reasonable hydrogen generating potential was also exhibited by the synthesized nanoparticles. As model fungi, Aspergillus niger and Mucor piriformis, are both significantly inhibited by AgFeO2 NPs, while M. piriformis is the target of the compound's greater antifungal action.

Isolation and characterization of quercetin from Prunus Serrulata leaf extract in the synthesis of Fe3O4 nanoparticles

Flavonoids and their derivatives have been known as reducing and capping agents for the synthesis of nanoparticles. These flavonoids are effective in the green synthesis of nanoparticles due to their environmentally friendly nature, low cost, and energy and time-saving assets. Generally, it is ignored which type of flavonoids were utilized in the synthesis of nanoparticles. This study presents the isolation and characterization of quercetin from Prunus Serrulata (P. Serrulata) leaf extract for the first time as the responsible reducing and capping agent in the synthesis of iron oxide nanoparticles (Fe3O4 NPs). The morphological characterization of the nanoparticles was performed by utilizing Scanning Electron Microscopy (SEM), Scanning Transmission Electron Microscopy (STEM), and Energy Dispersive X-ray Spectroscopy (EDX) analyses, whereas flavonoid characterization was completed through Ultraviolet–Visible Spectroscopy (UV–Vis), Fourier Transform-Infrared Spectroscopy (FT-IR), Liquid Chromatography-Mass Spectroscopy (LC-MS), and Nuclear Magnetic Resonance Spectroscopy (NMR). By using optimized conditions as 3:1 (Fe+3 solution: Prunus serrulata leaf extract) mixing ratio, 10 mM Fe+3 precursor, pH 6, and 25 °C reaction temperature, the average particle sizes of synthesized Fe3O4 NPs were ∼ 40 nm with the spherical shape. R2. Some quantitative results need to be added in the abstract.

Green synthesis of Iron oxide and Iron dioxide nanoparticles using Euphorbia tirucalli: characterization and antiproliferative evaluation against three breast cancer cell lines

Researchers have become increasingly interested in nanoparticles made from plants because of their stability and large surface area. In the current study, iron oxide and iron dioxide nanoparticles were synthesized using aerial parts of the E. tirucalli as a reducing agent. The nanoparticles were analyzed using various techniques, including Ultraviolet-visible spectroscopy, Fourier Transform Infrared spectroscopy, X-ray diffractometer, X-ray photoelectron spectroscopy, X-ray energy dispersive spectroscopy, Scanning electron Microscopy, and Transmission Electron Microscopy. The nanoparticles were then investigated for their antiproliferative effect against MCF-7, SK-BR-3, MDA-MB231, and Vero cell lines. The results confirmed the formation of FeO and FeO2 nanoparticles by color change and a UV absorbance peak between 220–390 nm. EDS analysis showed traces of Fe and O, while TEM confirmed the nanoparticle size of 100 nm. FTIR showed a peak at 514 nm. The FeO-RT NPs demonstrated over 80% antiproliferative activity against the MCF-7 cell line at a concentration of 10 μg/mL. while doxorubicin, FeO-RT NPs, and DCM extract showed similar activity against the MDA-MB231 cell line at 10 and 1 g/mL concentrations. However, Vero and SK-BR-3 cell lines showed decreased antiproliferative activity. This study highlights the environmentally friendly use and safe application of iron oxide NPs in cancer therapy.