Synthesis Of Iron Oxide Research Articles

Synthesis of a Novel Supermagnetic Fe3O4 Nanoparticles and their Congo Red Dye Removal, Cytotoxic, Antioxidant, and Antimicrobial Activities

Abstract Plantago lanceolata is a traditional medicinal plant that has attracted significant interest from researchers due to the use of its physiologically active components, particularly polyphenolics (flavonoids, hydroxycinnamic acids), in various fields. The aim of this study is to synthesize iron oxide (PLE@FeNPs) nanoparticles using a green synthesis approach with Plantago lanceolata (P. lanceolata) leaf extracts, characterize them, evaluate their in vitro effects, and assess their use in the removal of Congo red (CR) from wastewater. We carried out the physicochemical characterization of the nanoparticles using UV–Vis, FT-IR, and XRD spectroscopies; TEM and SEM microscopy; and Zetasizer particle size analysis. While the distinct peaks in XRD confirm the crystalline structure, TEM has determined an average particle size (8 nm) for PLE@NPs with deformed spherical nanoparticles. The FT-IR spectra showed that bioactive compounds from P. lanceolata were involved in the participation of PLE@FeNPs. EDX confirmed the presence of iron in the designed PLE@FeNPs. The antibacterial, antioxidant, and anticancer analyses of the studied PLE@FeNPs revealed significant activities. We investigated the adsorption kinetics of CR on PLE@FeNPs, taking into account initial dye concentration, different pH levels, adsorbent dosages, and temperature. At optimal conditions (concentration, 50 ppm; dosage, 15 mg; pH, 8), the degradation of CR dye in sunlight was found to be 99%. The small size of PLE@NPs (8 nm) and the more negative zeta potential (− 12.2 mV) support this situation. The equilibrium data demonstrated a good fit to the Langmuir isotherm model, outperforming the Freundlich isotherm model. The results showed that the pseudo-second-order kinetic model accurately described the kinetic data. PLE@NPs exhibited significant antioxidant, antimicrobial, and anticancer activities. This situation suggests that the nanocomposition of PLE@NPs obtained through the green route may have improved efficiency due to various synergistic effects. Overall, these results pave the way for further applications in dye removal and biological applications of environmentally friendly PLE@FeNPs. Graphical Abstract

Green Synthesis of Iron Oxide NPs (IONPs) by Using Aqueous Extract of Parthenium hysterophorus Linnaeus for the In-vitro Antidiabetic and Anti-inflammatory Activities

The Parthenium hysterophorus Linnaeus is one of the anti-inflammatory and antidiabetic ethnomedicine. Therefore the formulation of this plant as nanoparticles will be fruitful anti-inflammatory and antidiabetic as compared to conventional extract. In the current study, the aqueous kernel extract from Parthenium hysterophorus Linnaeus was subjected to synthesize iron oxide nanoparticles (IONPs) and explored their anti-inflammatory and anti-diabetic potentials. The results indicate that the aqueous kernel extract effectively produced IONPs, which were verified using standard analytical methods. UV-visible spectrophotometer analysis was used to check the formation of IONPs. The Fourier-transform infrared spectroscopy (FTIR) was used to check numerous functional groups from the valuable phytochemicals present in the extract. These functional groups play crucial roles as reducing, capping, and stabilizing agents during the synthesis of IONPs. Additionally, scanning electron microscopy (SEM) were utilized to investigate the surface characteristics of the nanoparticles. Notably, the IONPs fabricated from the extract demonstrated promising anti-inflammatory activity, inhibiting Human RBC by 79% and Heat Induced Hemolysis by 72%, as well as showing anti-diabetic potential with 60% inhibition of yeast glucose uptake and 72% inhibition of α-amylase activity, all at a concentration of 100 μg mL-1. These effects were partly comparable to standard drugs with anti-inflammatory activity of 85% inhibition of Human RBC and 78% inhibition of Heat Induced Hemolysis, and anti-diabetic activity of 67% inhibition of yeast glucose uptake and 78% inhibition of alpha amylase.

Green Synthesis of Iron Oxide from Lathe Waste Using Green Tea Leaves (<i>C</i><i>amellia</i><i> s</i><i>inensis</i>) Extract by Temperature Variations of Synthesis

Iron oxide was produced from lathe waste using green tea leaf extracts. Green tea leaves contain catechins, has been produced as a possible reducing, precipitating, stabilizing, and capping agent. Another advantage of applying green tea leaves to synthesize iron oxide is reducing toxicity. Various temperatures of synthesis utilizing the precipitation method proved successful in the formation of hematite. X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscope (SEM) were used to characterize the synthesis product. According to the XRD results, the magnetite transition phase was obtained after precipitation, while hematite formed after calcination. The crystallite sizes were 50.5 nm, 45.4 nm, and 39 nm, respectively. According to FTIR identification, the iron oxide was generated before and after calcination in the presence of a specific Fe-O group at the wavenumbers 553 cm-1 and 451 cm-1. The SEM results revealed that the particle size ranges from 4.61 nm – 20.74 nm, and the shape was not uniform, and aggregation.

Synthesis and evaluation of iron oxide nanoparticles from banana peel (Musa spp.) extract for the delivery of ciprofloxacin against resistant Escherichia coli

Background and objectiveResistance to antimicrobials is one of our most significant worldwide challenges. In Africa, around 31 % of the infections of urinary tract (UTIs) initiated by Escherichia coli (E. coli) have been observed to develop ciprofloxacin (CIP) resistance. As a result, significant efforts have been made to investigate novel and improved antibiotics. This study aimed at synthesizing iron oxide nanoparticles (IONPs) using banana peels (Musa Spp.) extract for delivery of CIP against resistant E. coli. MethodsA green synthesis method was used for the synthesis of IONPs using FeCl3.6H2O as a precursor and banana peel extract as a reducing and stabilizing agent. The physicochemical characteristics of the formed nanoparticles (NPs) were characterized using different methods. ResultsThe formation of hematite (α-Fe2O3) was confirmed with its FTIR characteristic peak at 461 cm−1, 542 cm−1, and 1131 cm−1. The size of synthesized IONPs was found to be 10.4 nm ± 1.98, 48 nm ± 0.9, and 67.3 nm ± 0.9 under XRD, SEM, and DLS measurements respectively. CIP-IONPs had almost the maximum drug loading capacity (33.3 % ± 0.67) with fast and slow drug release patterns at gastric and intestinal or blood pH respectively, and it had a promising resistant reversal with a zone of inhibition (ZOI) 22 mm ± 0.15 against resistance E. coli. ConclusionThe green synthesis of IONP using banana peel extract represents a novel and eco-friendly approach for the delivery of ciprofloxacin, with potential applications in addressing antimicrobial resistance.

Green Synthesis of Iron Nanoparticles Using Spinacia oleracea and Their Role in Antioxidant Defence

The green synthesis of iron oxide nanoparticles (Fe2O3) using Spinacia oleracea leaf extract is explored in this study. Iron oxide nanoparticles are noted for their unique properties, such as enhanced chemical reactivity due to their high specific surface area to volume ratios. Unlike traditional physical and chemical methods, green synthesis presents an environmental friendly alternative, leveraging biological processes for nanoparticle production. This method is particularly significant due to its potential applications in various fields, including medicine, where iron nanoparticles demonstrate antibacterial activity. However, limited research exists on their antioxidant properties. In this research, Spinacia oleracea leaf extract is utilized to synthesize iron oxide nanoparticles, followed by characterization using UV-Visible spectroscopy, FTIR, XRD, and SEM techniques. The results underscore the necessity for further investigation into the impact of nanoparticles on biological processes and the long-term effects of high nanoparticle concentrations on ecological stability. Additionally, this study includes an evaluation of antioxidant properties of the nanoparticles to address gaps in current research. Key Words Green synthesis, iron oxide, ecological stability, antioxidant, biological, nanoparticles.

Plant‐assisted synthesis of Fe3O4 nanoparticles for catalytic degradation of methyl orange dye and electrochemical sensing of nitrite

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

Assessing the Effect of Fe2O3 Nanoparticles on Catalase Activity in Patients with Chronic Periodontitis: In Vitro study and Molecular Docking

Periodontal disease, also known as gum disease, is a chronic inflammatory condition that affects the supporting structures of the teeth, including the gums and underlying bone. It is primarily caused by a bacterial infection resulting from poor oral hygiene practices. The main objectives of the current study were to synthesize iron oxide nanoparticles (Fe2O3-NPs) and their characteristics were analyzed through UV, SEM, and X-ray analysis. Additionally, the dispersion of the synthesized NPs was investigated using UV and TEM techniques. The study also aimed to assess the kinetic behavior and the impact of Fe2O3-NPs on catalase activity in the saliva of the patient and control groups. The findings revealed a significant increase in catalase activity (p>0.05) in both serum and saliva of all patient groups compared to the control group. The UV-visible spectrum shows that the absorption peaks for synthesized α- and γ-iron oxide nanoparticles was at 225 nm. According to the SEM image analysis, the primary particle size of the nano-particles is approximately 26.8 nm. The X-ray diffraction results indicate that the Fe2O3-NPs range in size from 14 nm to 26 nm. UV and TEM study conclude that water a suitable solvent for Fe2O3-NPs dispersion on kinetic study of catalase (CAT) activity. The kinetic data cleared that the α-Fe2O3-NPs have an inhibitory effect for the total activity of salivary CAT in the samples of both healthy and patients with chronic periodontitis. Lineweaver–Burk graph showed that (α-Fe2O3) inhibit catalase by un comp. inhibition. γ-Fe2O3-NPs inhibited total salivary CAT activity in healthy and patients with chronic periodontitis samples. Lineweaver –Burk graph showed that (γ-Fe2O3) inhibit catalase by uncompetitive inhibition.

Sodium titanate nanostructured modified by green synthesis of iron oxide for highly efficient photodegradation of dye contaminants

Abstract In this study, sodium titanate (ST)/iron oxide (Fe2O3) was successfully prepared as a novel binary photocatalyst for the first time to enhance the photocatalytic activity. The prepared photocatalyst was used in the photodegradation of methylene blue (MB) dye under sunlight and a tungsten lamp. The green synthesis method using orange peel extract was employed to prepare Fe2O3, while the hydrothermal method was used to synthesize ST. To achieve optimal photocatalytic efficiency, the loading of Fe2O3 onto ST was carefully controlled. The average crystallite size of ST, Fe2O3, and ST@Fe2O3 (with a 1:1 wt% ratio) was 999.8, 81.9, and 104 nm, respectively, using the Williamson–Hall (W–H) model. Optical analysis revealed that ST@Fe2O3 had a smaller direct bandgap (2.54 eV) compared to ST@0.3 Fe2O3 (2.70 eV) and ST@0.5 Fe2O3 (3.24 eV). The photodegradation of MB was analyzed considering the weight of the photocatalyst, the irradiation time, and the dye concentration. In-depth explanations of stability and kinetic models were also provided. Remarkably, the ST@Fe2O3 photocatalyst demonstrated superior performance compared to the other evaluated photocatalysts, completely degrading MB dye within just 60 min of solar light exposure. Incorporating Fe2O3 into ST effectively reduces the recombination of photo-produced electron/hole (e/h) pairs and broadens the response range of the solar spectrum. Based on these findings, ST@Fe2O3 appears to have a promising future as a practical photocatalyst for degrading various dye pollutants in wastewater.

Iron oxide Green synthesized nanoparticles for improved performance in Monolithic Dye Sensitized Solar Cells

In order to improve photovoltaic efficiency in Monolithic Dye-Sensitized Solar Cells (MDSSCs), this study examined the effects of incorporating green produced iron oxide nanoparticles to a nanoporous carbon counter electrode. An extract from the leaves of Ocimum gratissimum was effectively used to synthesize iron oxide nanoparticles. The development of iron oxide nanoparticles was verified by optical absorption in the 350–450 nm range. With an average crystallite size of 47.9 nm, XRD patterns demonstrated the crystalline nature of the Iron oxide nanoparticles. Chemical bonds that may responsible for the nanoparticle production were found using FTIR investigations. An impressive 135.3% boost in efficiency was recorded for cell containing the Iron oxide nanoparticles, according to the MDSSC performance evaluation where DSSC without nanoparticles had a lower solar-to-electric power conversion efficiency of 1.7%, an open circuit voltage of 0.2625 V, a short-circuit current of 0.0723 mA/cm2, and a fill factor of 0.3630. The FeO CEs cell had an open-circuit voltage of 0.4274 V, a short-circuit current of 0.1042 mA/cm2, and a fill factor of 0.46. Their solar-to-electric power conversion efficiency was 4.0%. The potential of incorporating green-synthesised iron oxide nanoparticles into MDSSC counter electrode was shown by their great biocompatibility and even dispersion.

Fast and green synthesis of iron oxide using low-power laser sintering on reduced graphene oxide sensor for ammonia gas detection

Oxide materials are important for gas sensing applications. Unfortunately, most of the synthesis methods use many toxic chemicals and need long calcination at high temperatures. Thus, developing simple and green synthesis processes, which can be performed fast and at low temperatures, is imperative for both industrial manufacturers and our environment. Here, our fast and green synthesis method based on low-power laser sintering for producing FeOx (with Fe2O3 as the main composition) is presented. Besides, FeOx particles were decorated on reduced graphene oxide (RGO) to form a resistive sensor. Notably, our FeOx material can reduce the response of RGO toward acidic gas (NO2) but it enhances the RGO response toward the basic NH3 gas. Particularly, our hybrid FeOx/RGO sensor can detect NH3 gas at above 2 ppm under dry and humidified conditions (<85 % RH). That effect of FeOx is found due to the formation of alpha-phase Fe2O3 which acts as a p-type semiconductor, which is explored and explained in the discussion section. Finally, our findings not only reveal the potential of our hybrid sensing materials for practical NH3 sensing applications but also confirm the usefulness of laser-sintering to produce catalytic oxide materials environmentally friendly and at low cost.

Aspergillus Oryzae Mediated α‐Fe2O3 Nanoparticles for Photocatalytic Remediation of Basic Fuschin Dye and Antimicrobial Activities

AbstractGreen synthetic approach for the synthesis of Iron oxide (α‐Fe2O3) nanoparticles were successfully carried out using Aspergillus oryzae culture mediated biogenic route. The synthesized nanoparticle was confirmed by structural and optical characterization with the help of hematite phase. The α‐Fe2O3 nanoparticles show antimicrobial activity against bacterial strains Staphylococcus aureus, Pseudomonas aeruginosa and fungal strain Candida albicans. Under visible light, the α‐Fe2O3 nanoparticles demonstrate remarkable antibacterial action, confirming their superior efficacy for photocatalytic remediation. The present study discloses that the α‐Fe2O3 nanoparticles are efficient photocatalysts for 96 % degradation of basic fuchsin dye and highly active antimicrobial agent.

Synthesize Iron Oxide and Zinc Oxide Nanoparticles Using Plant Extracts

Recently, a plant-mediated approach to synthesizing nanoparticles via unconventional, eco-friendly technique-based techniques involving natural materials was developed. In this work, the microwave method has been used, where Hibiscus rosa sinensis flower extract and Myristica Fragrans have been used as reducers and stabilizers to synthesize iron oxide nanoparticles (α-Fe2O3) and zinc oxide nanoparticles (ZnO), respectively. The melting point and ultraviolet-visible spectrometer (UV-Vis) have been utilized to investigated and characterized the synthesized iron oxide and Zinc oxide nanoparticles. The results showed that the melting point of Fe2O3-NPs and ZnO-NPs were above ~300 °C, which indicated the melting of nanoparticle. Nanoparticles exhibit a significant in melting point as their size goes below ≈10 nm. in addition, the UV-Vis absorption spectra of the synthesized iron oxide NPS show peak surface plasmon resonance (SPR) band around 320 nm and Zinc oxide NPS shown peak surface plasmon resonance (SPR) band around 370 nm. The microwave method has been successfully used in this study, which has advantages over the other methods.

Piper chaba Stem Extract Facilitated the Synthesis of Iron Oxide Nanoparticles as an Adsorbent to Remove Congo Red Dye.

In this study, a straightforward, eco-friendly, and facile method for synthesizing iron oxide nanoparticles (IONPs) utilizing Piper chaba steam extract as a reducing and stabilizing agent has been demonstrated. The formation of stable IONPs coated with organic moieties was confirmed from UV-vis, FTIR, and EDX spectroscopy and DLS analysis. The produced IONPs are sufficiently crystalline to be superparamagnetic having a saturation magnetization value of 58 emu/g, and their spherical form and size of 9 nm were verified by XRD, VSM, SEM, and TEM investigations. In addition, the synthesized IONPs exhibited notable effectiveness in the removal of Congo Red (CR) dye with a maximum adsorption capacity of 88 mg/g. The adsorption kinetics followed pseudo-second-order kinetics, meaning the adsorption of CR on IONPs is mostly controlled by chemisorption. The adsorption isotherms of CR on the surface of IONPs follow the Langmuir isotherm model, indicating the monolayer adsorption on the homogeneous surface of IONPs through adsorbate-adsorbent interaction. The IONPs have revealed good potential for their reusability, with the adsorption efficiency remaining at about 85% after five adsorption-desorption cycles. The large-scale, safe, and cost-effective manufacturing of IONPs is made possible by this environmentally friendly process.

Electrocatalysis of Oxygen Evolution Reaction by Iron Oxide Nanomaterials Synthesized with Camellia sinensis Extract

The generation of clean, zero-carbon, and renewable energy is a challenge for the development of a sustainable and egalitarian society. Hydrogen gas can be produced by water electrolysis and has been claimed as the most promising option to replace fossil fuels. The oxygen evolution reaction (OER) is the most energetically demanding step of the water splitting and requires the use of electrocatalysts to overcome the kinetic barrier. Iron oxide nanomaterials have been emerging as a low-cost and Earth-abundant OER electrocatalysts. The synthesis of iron oxide assisted by plant extract is an eco-friendly approach to obtain nanomaterials with unique properties. Herein, we investigated iron oxide synthesized with the assistance of Camellia sinensis extract, under different experimental conditions towards oxygen evolution reaction electrocatalysis. Pure phases of iron oxide were obtained, ferrihydrite and maghemite showed overpotentials of 460 and 480 mV at a current density of 10 mA cm−2 , respectively. After calcination, hematite was formed and the overpotential was raised to 610 and 810 mV, respectively. The lower overpotential of the amorphous materials could be related to the lower electron transfer resistance and faster reaction rate. On the other hand, the calcinated materials presented higher specific activity, stability and higher Faradaic efficiency.

Ferromagnetic Enhancement of Microcrystalline Cellulose via Chemical Reduction Method

Iron oxide nanoparticles (NPs) have potential in biological, biomedical, and environmental applications because of their magnetic susceptibility, stability, and biocompatibility characteristics. However, it also has limitations, such as the aggregation of magnetic NP. Thus, the outer surface of the particles should be modified by coating materials. This paper focused on synthesizing iron oxide by chemical reduction method and coating it with Fe(III) nitrate, PVP, and hydrazine. The coating solution at two different concentrations was prepared to determine effective and economical usage conditions. The effect of coating iron oxide with microcrystalline cellulose (MCC) was conducted at different concentrations of iron oxide on the nanomaterials with respect to morphological, thermal, and magnetic susceptibility. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicated good morphology images of FeNp-MCC. Energy dispersive X-ray (EDX) spectra reveal the presence of carbon, oxygen, and iron in the synthesized microparticles.TGA analysis showed iron material was succesfully formed into the surface of microcrystalline cellulose. Lastly,the magnetism results proved that cellulose is strongly interacting with magnetite nanoparticles.

Novel mesoporous iron oxide synthesized from naturally occurring magnetic sand: A potential and promising catalyst for chemical processes

This paper presents the synthesis of iron oxide from natural magnetic sand that was obtained from Michika, Adamawa State, Nigeria. Characterization of the raw magnetic sand and the synthesized iron oxide was performed to investigate the effect of the synthesis method on functional groups, morphology, composition, crystallinity, acidity and surface area/pore distribution using Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy – energy dispersive X-ray (SEM – EDX), X-ray fluorescence (XRF), X-ray diffraction (XRD), BET and pyridine FTIR, respectively. The XRF analysis of the two samples revealed a significant variation in oxide composition. The raw magnetic sand had an iron oxide content of 64.69 wt%, which increased to 85.20 wt% after synthesis. Furthermore, the SEM-EDX analysis indicated a decrease in average particle size from 114.6 and 36.8 µm for the respective samples. The XRD patterns revealed that the crystallinity increased after synthesis. FTIR showed the associations of functional groups present in the sample. The wavebands in the range 550 – 630 cm−1, which correspond to the Fe – O bond, improved clearly in the synthesized iron oxide sample, particularly at 582 cm−1. The pyridine FTIR depicts that the overall acidic site is higher in the synthesized sample. The N2 adsorption–desorption procedure shows an increased BET surface area from 9.394 m2/g (raw) to 24.851 m2/g (synthesized). Overall, the results showed that the synthesized mesoporous iron oxide exhibits properties similar to materials that have a high potential for application as catalysts in chemical processes.

Synthesis and characterization of iron oxides and their application as inorganic pigments in white paint

AbstractThe tones of iron oxide pigments range from yellow, red, brown and green to black. Iron oxide pigments are non‐toxic and have a nanometric particle size, which makes them ideal for use as pigments. The current study synthesised synthetic inorganic pigments based on iron oxides using the alkaline precipitation method. This approach to the synthesis of iron oxide pigments makes them less expensive for obtaining reproducible colours. Iron salts (iron (III) chloride, iron (III) nitrate, iron (II) sulphate [ferrous sulphate] and iron (III) sulphate) have been combined with alkaline solutions (sodium hydroxide, potassium hydroxide and ammonium hydroxide) to form coloured iron oxides, which are widely known as natural inorganic pigments. The 12 samples produced in four different colours (red, yellow, brown and black) were left in aqueous suspension and dispersed in commercial real white estate paint, to evaluate their behaviour as pigments. Structural characterisation (X‐ray diffractometry), composition (X‐ray fluorescence by dispersive energy), thermal analysis (i.e. thermogravimetric analysis and the differential thermal analysis) and spectroscopy (FTIR and photoacoustic), as well as colorimetry, were performed. The phases indexed by X‐ray diffractometry were goethite, haematite, magnetite and lepidocrocite. The inorganic pigments produced are compatible with natural inorganic pigments. They also showed dispersion compatibility in commercial white paint without changing the surface coating powder and are therefore an alternative to synthetic inorganic pigments.

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.

Photothermally heated colloidal synthesis of nanoparticles driven by silica-encapsulated plasmonic heat sources

Using photons to drive chemical reactions has become an increasingly important field of chemistry. Plasmonic materials can provide a means to introduce the energy necessary for nucleation and growth of nanoparticles by efficiently converting visible and infrared light to heat. Moreover, the formation of crystalline nanoparticles has yet to be included in the extensive list of plasmonic photothermal processes. Herein, we establish a light-assisted colloidal synthesis of iron oxide, silver, and palladium nanoparticles by utilizing silica-encapsulated gold bipyramids as plasmonic heat sources. Our work shows that the silica surface chemistry and localized thermal hotspot generated by the plasmonic nanoparticles play crucial roles in the formation mechanism, enabling nucleation and growth at temperatures considerably lower than conventional heating. Additionally, the photothermal method is extended to anisotropic geometries and can be applied to obtain intricate assemblies inaccessible otherwise. This study enables photothermally heated nanoparticle synthesis in solution through the plasmonic effect and demonstrates the potential of this methodology.

Photocatalytic Removal of Crystal Violet Dye Utilizing Greenly Synthesized Iron Oxide Nanoparticles

The presence of synthetic industrial dyes in the environment poses significant risks to aquatic ecosystems, human health, and economies. This study aims to synthesize iron oxide nanoparticles (IONPs) using a green method, analyze them using physicochemical techniques, and examine the effectiveness with which they photocatalytically degrade crystal violet dye in sunlight. Fourier transform infrared spectroscopy (FTIR) analysis revealed that the biogenic IONPs showed a UV peak at a wavelength of 241 nm, with functional groups including phenols, alkynes, and alkenes. X-ray diffraction (XRD) analysis confirmed the amorphous nature of the bioinspired IONPs. The mean diameter of the biogenic IONPs was 49.63 ± 9.23 nm, and they had a surface charge of −5.69 mV. The efficiency with which the synthesized IONPs removed the crystal violet dye was evaluated under dark and sunlight conditions. The removal efficiency was found to be concentration and time dependent, with a peak removal percentage of 99.23% being achieved when the IONPs were exposed to sunlight for 210 min. The biogenic IONPs also demonstrated antioxidant activity, with a relative IC50 value of 64.31 µg/mL. In conclusion, biogenic IONPs offer a viable and environmentally friendly approach for eradicating industrial synthetic dyes and remediating contaminated environments and aquatic ecosystems.