Extract Nanoparticles Research Articles

Evaluation of extraction and storage conditions for quantification and characterization of silver nanoparticles in complex samples by single particle-ICP-MS

The extraction of nanoparticles (NPs) from complex matrices and subsequent storage can potentially alter the NPs physicochemical properties and hinder cross-study comparisons. Most NP extraction methods are designed and tested at high nanoparticle concentrations, although (eco)toxicological and regulatory monitoring programs require methods capable of analyzing NPs at environmentally relevant concentrations (lower ppb range). In this study, we investigated how extraction methods affect the characteristics of PVP coated and citrate-stabilized silver NPs (AgNPs) spiked into soil, sewage sludge, and biological samples at environmentally relevant concentrations using Single Particle Inductively Coupled Plasma Mass Spectrometry spICP-MS). Further we investigated the impact of storage temperature (-80°C to 21°C) and storage duration (1-28 days) on the particle characteristics such as particle size.We found that aqueous AgNPs samples with low ionic strength media retained their original characteristics (like particle size, particle concentration and particle-based Ag mass) when preserved at 4°C for up to 28 days. AgNPs dispersed in high ionic strength media were however better preserved at -80°C. Among the extraction agents, tetrasodium pyrophosphate was more efficient in extracting AgNPs from soil and sewage sludge matrices, while Proteinase K was more suitable for biological samples from organisms (earthworms or fish).Although our study focused only on AgNPs, it provides crucial information to aid interlaboratory comparisons and data interpretation for (eco)toxicological studies.

Preparation, physical properties, and evaluation of antioxidant capacity of aqueous grape extract loaded in chitosan-TPP nanoparticles.

Grape extract is reportedly rich in phenolic compounds that possess strong antioxidant activities. Encapsulation of such extracts in nanoparticles (NPs) is an effective way to preserve various food products. In the present study, grapes were first extracted, and the amount of total phenolic content and different types of phenolic acids was determined. The extracts at different chitosan/extract weight ratios (1:0.25, 1:0.5, 1:0.75, and 1:1) were then encapsulated in chitosan nanoparticles (NPs) using the ionic gelation method. The extract‐loaded chitosan nanoparticles were characterized by their physicochemical properties using the dynamic light scattering (DLS) technique, chemical properties using Fourier‐transform infrared (FTIR) spectroscopy, and X‐ray powder diffraction technique (XRD), the morphological properties using scanning electron microscopy (SEM), and the antioxidant activity using the 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) test. The encapsulation efficiency (EE) and loading capacity (LC) were also assessed. Our findings showed that the free radical inhibition effect of NPs significantly increased with an increase in extract concentration. Chitosan NPs presented acceptable encapsulation efficiency and loading capacity (LC), and the encapsulation process enhanced the antioxidant activity of the free grape extracts. At the weight ratio of 1:0.5, the particle size and zeta potential of the NPs were 177.5 ± 2.12 nm and 32.95 ± 0.49 mV, respectively. FTIR and XRD analyses verified the credibility of the encapsulated grape extract in chitosan NPs. These NPs can be an efficient way to increase the shelf‐life of food products.

Simple Method for the Extraction and Determination of Ti-, Zn-, Ag-, and Au-Containing Nanoparticles in Sediments Using Single-Particle Inductively Coupled Plasma Mass Spectrometry.

The quantitative analysis of nanoparticles (NPs) in the environment is significantly important for the exploration of the occurrence, fate, and toxicological behaviors of NPs and their subsequent environmental risks. Some protocols have been recommended for the separation and extraction of NPs that are potentially dispersed in complex environmental matrixes, e.g. sediments and soils, but they remain limited. However, certain factors that may significantly affect extraction efficiency have not been comprehensively explored. In this study, on the basis of the single-particle inductively coupled plasma mass spectrometry (SP-ICP-MS) technique, a simple standardized protocol for separating and analyzing metal-containing NPs in sediment samples was developed. On consideration of the extraction efficiencies of indigenous NPs (Ti- and Zn-NPs) and spiked NPs (Ag- and Au-NPs) in sediments, sedimentation with a settling time of 6 h is recommended for the separation of NPs and large particles, and the optimal sediment to water ratio, ultrasonication power, time, and temperature are 0.4 mg/mL, 285 W, 20 min, and 15-25 °C, respectively. On the basis of the optimized method, the recoveries of spiked Ag and Au-NPs were 71.4% and 81.1%, respectively. The applicability of the optimal protocols was verified, and TOC was proved to be an important factor controlling the separation and extraction of NPs in environmental samples. The separation and extraction of NPs in elevated TOC samples can be improved by increasing the ultrasonication power, time, and temperature.

Green emitting rare earth Gd2O3:Tb3+ nanoparticles for rapid imaging of latent fingerprint

A series of green emitting Gd2O3:Tb3+ (Tb: 0%–10% mol) nanoparticles (NP) were synthesized using the hydrothermal method, then characterized and evaluated for latent fingerprint visualization. X-ray diffraction study (XRD) revealed a cubic structure of the nanoparticles and the total incorporation of the terbium in the Gd2O3 matrix. Field Emission-Scanning Electron Microscopy (FESEM), Energy Dispersive x-ray Spectrometry (EDX) and Transmission Electron Microscopy (TEM) were used to study the morphology and the elementary composition of the NP. Photoluminescence (PL) studies showed strong green emission around 540 nm due to the transition 5D4 → 7F5. The luminescence color of the synthesized NP was characterized by the CIE 1931 chromaticity diagram. The potential use of the NP powders for the visualization of latent fingerprint under UV irradiation was assessed on various substrates. The latent fingerprint images revealed by the Gd2O3:Tb3+ NP powders are clear enough to extract and analyze reliable fingerprint features. The fingerprint quality was evaluated using three fingerprint quality assessment metrics and by extracting and measuring the visibility of the minutiae. The experimental results show very good quality images of the latent fingerprint acquired using the Gd2O3:Tb3+ NP and yield good minutiae extraction.

Mechanistic Aspects of Simultaneous Extraction of Silver and Gold Nanoparticles across Aqueous-Organic Interfaces by Surface Active Iron Oxide Nanoparticles.

Surface active iron oxide nanoparticles (NPs) were used for the simultaneous extraction of water soluble Ag and Au NPs across an aqueous-organic interface from aqueous bulk. The surface activity of iron oxide NPs was achieved by using cationic Gemini surfactants of different architectures during the in situ synthesis of iron oxide NPs in hydrothermal synthesis. Aqueous bulk solubility of Ag and Au NPs was achieved by stabilizing them with conventional surfactants of different polarities such as SDS, CTAB, and DDM. The amphiphilic nature of iron oxide NPs demonstrated their remarkable ability to extract Ag and Au NPs through both hydrophilic and hydrophobic interactions. The mechanism of extraction from aqueous bulk was monitored by placing different amounts of surface active iron oxide NPs on the aqueous-organic interface and was studied with the help of UV-visible, DLS, and IR measurements. XPS and TEM measurements were used for the quantitative estimation of efficiency of extraction. Extraction was facilitated when both hydrophilic and hydrophobic interactions were participating simultaneously. Results may help in designing a suitable method for purification of industrial effluents contaminated with metal particulates simply by applying an external magnetic field rather than going through a complicated conventional filtration process.

Multistep Method to Extract Moderately Soluble Copper Oxide Nanoparticles from Soil for Quantification and Characterization.

The objective of this study is to assess how method parameters impact the extraction of moderately soluble CuO nanoparticles (NPs) from a standard natural soil (LUFA 2.1) suitable for chemical analysis. The extraction procedure is comprised of three steps: (i) preconditioning the soil to increase the sodium adsorption ratio, (ii) extracting colloids/NPs from the soil matrix using sonication and a dispersing agent, and (iii) separating the dissolved and nanoparticulate CuO fractions using cloud point extraction. Method parameters of the extraction procedure, including sonication, number of extraction cycles, and dispersing agent, were adjusted to achieve the highest extraction of CuO NPs, while minimizing dissolution. The maximum recovery of CuO NPs ranged from 31% to 42% for an amended concentration range of 10-250 mg-Cu (kg soil)-1 using a preconditioning step to exchange divalent cations for monovalent ions, 0.2% carboxymethyl cellulose (CMC) 700 kg mol-1 as the dispersing agent, probe sonication for 1 min, 3 extraction cycles, and a 1:10 soil-to-liquid ratio. CuO NPs that are polyvinylpyrrolidone (PVP)-coated with a greater stability against aggregation had significantly higher extractability and dissolution. This procedure is the first to effectively extract moderately soluble NPs from soil and experimentally separate them from their dissolved fraction and can be applied to other moderately soluble metal containing natural, incidental, or engineered NPs in soil.

Green pyomelanin-mediated synthesis of gold nanoparticles: modelling and design, physico-chemical and biological characteristics

BackgroundSynthesis of nanoparticles (NPs) and their incorporation in materials are amongst the most studied topics in chemistry, physics and material science. Gold NPs have applications in medicine due to their antibacterial and anticancer activities, in biomedical imaging and diagnostic test. Despite chemical synthesis of NPs are well characterized and controlled, they rely on the utilization of harsh chemical conditions and organic solvent and generate toxic residues. Therefore, greener and more sustainable alternative methods for NPs synthesis have been developed recently. These methods use microorganisms, mainly yeast or yeast cell extract. NPs synthesis with culture supernatants are most of the time the preferred method since it facilitates the purification scheme for the recovery of the NPs. Extraction of NPs, formed within the cells or cell-wall, is laborious, time-consuming and are not cost effective. The bioactivities of NPs, namely antimicrobial and anticancer, are known to be related to NPs shape, size and size distribution.ResultsHerein, we reported on the green synthesis of gold nanoparticles (AuNPs) mediated by pyomelanin purified from the yeast Yarrowia lipolytica. A three levels four factorial Box–Behnken Design (BBD) was used to evaluate the influence of temperature, pH, gold salt and pyomelanin concentration on the nanoparticle size distribution. Based on the BBD, a quadratic model was established and was applied to predict the experimental parameters that yield to AuNPs with specific size. The synthesized nanoparticles with median size value of 104 nm were of nanocrystalline structure, mostly polygonal or spherical. They exhibited a high colloidal stability with zeta potential of − 28.96 mV and a moderate polydispersity index of 0.267. The absence of cytotoxicity of the AuNPs was investigated on two mammalian cell lines, namely mouse fibroblasts (NIH3T3) and human osteosarcoma cells (U2OS). Cell viability was only reduced at AuNPs concentration higher than 160 µg/mL. Moreover, they did not affect on the cell morphology.ConclusionOur results indicate that different process parameters affect significantly nanoparticles size however with the mathematical model it is possible to define the size of AuNPs. Moreover, this melanin-based gold nanoparticles showed neither cytotoxicity effect nor altered cell morphology.

A ternary nanostructured α-Fe2O3/Au/TiO2 photoanode with reconstructed interfaces for efficient photoelectrocatalytic water splitting

In this study, a ternary nanostructured α-Fe2O3/Au/TiO2 film with integrating a crystalline α-Fe2O3 core, metallic Au nanoparticles (NPs), and an amorphous TiO2 overlayer is fabricated and examined as a photoanode for photoelectrocatalytic water splitting. Under simulated solar illumination, the as-prepared photoanode exhibits a four-fold increase (1.05 mA cm−2) in photocurrent density at 1.23 V versus reversible hydrogen electrode (RHE) relative to bare α-Fe2O3. Based on systematic investigations, it is proposed that Au NPs extract photoholes from the bulk of α-Fe2O3 core and then shuttle them to the outer TiO2 overlayer, and meanwhile, TiO2 overlayer efficiently captures and stores the photoholes and facilitates the hole injection into electrolyte. Thus, the remarkably improved photoelectrocatalytic water splitting performance of α-Fe2O3/Au/TiO2 photoanode is attributed to the significantly suppressed bulk and surface charge recombination due to the relayed pumping of the photogenerated charge carriers through the photoanode/electrolyte interfaces reconstructed by Au NPs and TiO2 overlayer.

Anti-Candida Biofilm Activity of Pterostilbene or Crude Extract from Non-Fermented Grape Pomace Entrapped in Biopolymeric Nanoparticles.

Polymeric nanoparticle-based carriers are promising agents to deliver drugs to cells. Vitis vinifera phenolic compounds are known for their antifungal activity against Candida albicans. The aim of the present study was to investigate the antifungal activity of pterostilbene or crude extracts from non-fermented grape pomace, entrapped in poly(lactic-co-glycolic) acid nanoparticles (NPs), with diameters of 50 and 150 nm, on Candida biofilm. The fluorescent probe coumarin 6 was used to study the uptake of poly(lactic-co-glycolic)acid (PLGA) NPs in planktonic cells and biofilm. The green fluorescent signal of coumarin 6 was observed in Candida biofilm after 24 and 48 hours. Both pterostilbene and crude pomace extract entrapped in NPs exerted a significantly higher anti-biofilm activity compared to their free forms. The entrapment efficiency of both pterostilbene and crude pomace extract in PLGA NPs was ~90%. At 16 µg/mL, pterostilbene loaded in PLGA NPs reduced biofilm formation of 63% and reduced mature biofilm of 50%. Moreover, at 50 µg/mL, the pomace extract loaded in NPs reduced mature biofilm of 37%. These results strongly suggest that PLGA NPs are promising nanodevices for the delivery of antifungal drugs as the crude grape pomace extract, a by-product of white wine making.

Nanoparticles Used for Extraction of Polycyclic Aromatic Hydrocarbons

This article offers a review on the application of nanoparticles (NPs) that have been used as sorbents in the analysis of polycyclic aromatic hydrocarbons (PAHs). The novel advances in the application of carbon NPs, mesoporous silica NPs, metal, metal oxides, and magnetic and magnetised NPs in the extraction of PAHs from matrix solutions were discussed. The extraction techniques used to isolate PAHs have been highlighted including their advantages and limitations. Methods for preparing NPs and optimized conditions of NPs extraction efficiency have been overviewed since proper extraction procedures were necessary to achieve optimum analytical results. The aim was to provide an overview of current knowledge and information in order to assess the need for further exploration that can lead to an efficient and optimum analysis of PAHs.

A high-throughput analytical tool for quantification of 15 metallic nanoparticles supported on carbon black

Metallic nanoparticles (NPs) have been widely used in different areas of science. Usually, they are immobilized on a low-cost support for catalysis purposes. However, there is a lack of studies for specific methods for analytical quantification since the extraction of these metallic NPs from the matrix is still a challenge. In this work, 15 metallic NPs were synthesized (Pt, Pd, Au, Ag, Rh, Ru, Nb, Mn, Co, Cu, Zr, Sn, Ce, Ni and W) supported on a commercial carbon black (Vulcan XC72). Then, six different methods were employed for sample preparation and further determination by Inductively Coupled Plasma Mass Spectrometry (ICP-MS). The results can be divided in three groups concerning the extraction of metallic NPs: the first group could be extracted from the matrix with nitric acid, for the second one it was necessary to employ a digestion at 25 °C (room temperature), and finally a third group which was found to be independent of acid and temperature. These findings can contribute to future research in the field of catalysis to improve their characterization regarding the metallic NPs.

Impact of metal nanoparticles on biogas production from poultry litter

The effects of metal nanoparticle (NP) addition during anaerobic digestion (AD) of poultry litter was tested using two sequential experiments: Exp. A) four NPs (Fe, Ni, Co, and Fe3O4) at three concentrations; and Exp. B) NP combinations (Fe, Ni, and Co) at four concentrations. Scanning electronic microscopy (SEM) and elemental analysis were used to confirm NP inclusion after dispersion (before AD) and track nanoparticles post-AD, and new technique for NP extraction post-AD was developed. Before AD, NPs ranged from 30.0 to 80.9 nm for Fe, Ni, and Co, and 94.3 to 400 nm for Fe3O4. Methane production increased with NPs addition compared to poultry litter-only, with the highest increases observed with NPs concentrations (in mg/L) of 12 Ni (38.4% increase), 5.4 Co (29.7% increase), 100 Fe (29.1% increase), and 15 Fe3O4 (27.5% increase). Nanoparticle mixtures greatly decreased H2S production. The SEM post-AD detected Fe, Ni, and Fe3O4 at concentrations ≥100 mg/L.

Polypyrrole‐modified magnetic nanoparticles for preconcentration of atorvastatin in human serum prior to its determination using high‐performance liquid chromatography

In the current study, the successful application of polypyrrole-Fe3O4 nanoparticles (NPs) was investigated as a suitable sorbent in the magnetic-dispersive solid phase extraction mode to the preconcentration and determination of atorvastatin (AT) in human serum by high-performance liquid chromatography-ultraviolet detection. Iron oxide NPs were prepared by co-precipitation method and the polypyrrole compound was used to modify their surface. The structure and NP size of Fe3O4@PPy NPs were characterised by Fourier-transform infrared technique and scanning electron microscopy. Some factors affecting the extraction efficiency, including the pH value, amount of sorbent, extraction time, elution type and its volume and desorption time were optimised. Under the optimum conditions, magnetic NPs extraction of standard solution of AT showed a linear calibration curve in the range of 0.1–1000 μg l−1 with R 2 = 0.9962. The method was sensitive, with a low limit of detection (0.10 μg l−1) and quantification (0.38 μg l−1). The relative standard deviation of five extractions at the concentration level of 0.1 μg l−1 was 4.2. Good recoveries (92.00–98.10%) with low relative standard deviations (6.0–2.4%) indicated that the matrices do not significantly affect the extraction process. Finally, the proposed method was successfully used to measure AT in human serum samples.

Analysis of gold and silver nanoparticles internalized by zebrafish (Danio rerio) using single particle-inductively coupled plasma-mass spectrometry

With the increase in the application of nano-consumer products containing engineered nanoparticles (NPs), the unintended environmental exposure to NPs has been inevitable. Because of the bioaccumulation of NPs, concern about their potential cytotoxicity to aquatic organisms is also growing. Although measuring tools for analyzing particle size and/or concentration of NPs in intracellular uptake of tissues have been well developed, a simultaneous analysis of the two characteristics is difficult. The objective of this study was to use single particle-inductively coupled plasma-mass spectrometry (sp-ICP-MS) to measure the bioaccumulation and particle size changes of NPs exposed to zebrafish (Danio rerio) for 7 days. The uptake of NPs in the liver, intestine, and gill tissues was confirmed by electron microscopic (EM) analysis. However, the primary particle size of NPs in tissues could not be determined by the EM analysis. Therefore, sp-ICP-MS coupled with alkaline digestion was used for the easy extraction and immediate analysis of NPs from tissues. Zebrafish were exposed to four NPs (30 and 80 nm gold/silver NPs; AuNPs/AgNPs). Uptake amounts of AgNPs in the liver and intestine were significantly higher than those of AuNPs. Although larger NPs were finally accumulated in the liver and intestine tissues, most of the smaller NPs were filtered in the gills. The sp-ICP-MS method coupled with alkaline digestion enabled the accurate analysis of size, size distribution, and mass concentration of NPs in an aquatic organism.

Extracellular biosynthesis of silver nanoparticles from Cyanobacteria

The field of nanotechnology is being now extensively studied by researchers particularly synthesis of nanoparticles with non-toxic, environmentally benign techniques and using mainly microorganisms including bacteria, fungi and algae. These bio-synthesized nanoparticles are aimed to be used as alternatives to the medical agents; however, their activity depends on their size, morphology, distribution and the source of bio synthesis. In this study silver nanoparticles were synthesized from three types of Cyanobacteria naming Nostoc sp., Scytonema sp. and Phormidium sp. Higher antibacterial activity was obtained with Scytonema Nanoparticles (NP) extracts against MRSA followed by Phormidium sp. compared to other algal NP extracts against Staphylococcus aureus, E. coli and Pseudomonas aeruginosa. Chemical analysis of the studied algal NP extracts revealed higher peaks at 3278 cm-1 and 3262 cm-1 for Phormidium and Nostoc algal species, indicating the presence of NP particles to which the antibacterial activity is being attributed.

Quantitative Aspect of Leucophyllum frutescens Fraction before and after Encapsulation in Polymeric Nanoparticles.

The interest on plants has been focalized due to their biological activities. Extracts or fractions from plants in biodegradable polymeric nanoparticles (NP) provide many advantages on application studies. The encapsulation of the extract or fraction in NP is determined for the establishment of the test dose. HPLC method is an alternative to calculate this parameter. An analytical method based on HPLC for quantification of a hexane fraction from L. frutescens was developed and validated according to ICH. Different concentrations of the hexane fraction from leaves (HFL) were prepared (100–600 μg/mL). Linearity, limit of detection, limit of quantification, and intra- and interday precision parameters were determined. HFL was encapsulated by nanoprecipitation technique and analyzed by HPLC for quantitative aspect. The method was linear and precise for the quantification of the HFL components. NP size was 190 nm with homogeneous size distribution. Through validation method, it was determined that the encapsulation of components (1), (2), (3), and (4) was 44, 74, 86, and 97%, respectively. A simple, repeatable, and reproducible methodology was developed for the propose of quantifying the components of a vegetable material loaded in NP, using as a model the hexane fraction of L. frutescens leaves.

The effect of Sambucus nigra L. extract and phytosinthesized gold nanoparticles on diabetic rats

Nanomaterials such as gold nanoparticles (NPs) conjugated with natural products have shown good results in lowering the glycated hemoglobin and have an anti-inflamatory effect. The aim of our study is to evaluate the antidiabetic effect of NPs functionalized with Sambucus nigra L. (SN) extract on experimental model of diabetes in rats. Diabetes was induced to 18 Wistar male rats (n=6) by a single intramuscular injection of streptozotocin (30mg/kg body weight − b.w.). SN extract (15mg/kg b.w.), NPs (0.3mg/kg b.w.) and vehicle (normal saline) were administered by gavage once a day, every morning, for 2 weeks. Other 18 animals were used as control groups and were treated with the same compounds, at the same time. Afterwards, blood, liver and muscle samples were taken to assess the oxidant/antioxidant status and the liver for the evaluation of metalloproteinases (MMP)-2 and 9 activities, COX-2 and NFKB expressions and for immunohistochemistry. Serum glycemia, cholesterol, alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT) were also measured.The administration of NPs extract increased the muscle and systemic GSH/GSSG ratio in the diabetic group vs. diabetic (p<0.03) or non-diabetic groups treated with vehicle (p<0.05) and decreased MDA levels compared to non-diabetic group (p<0.05). COX-2 expression (p<0.0001) and proMMP-2 activity (p<0.05) decreased after pretreatment with NPs in parallel with the reduction of Kupffer cells percent (<0.001). No morphological abnormalities were detected in histopathology. NPs present a great potential for further usage as adjuvants in the diabetic therapy due to the increase of antioxidant defence and reduction of MMPs activity and inflammation in liver tissue.

Insights into the Partitioning Behavior of Secondary Surfactants in a Microemulsion-Based Synthesis of Metal Nanoparticles: A DLS and 2D NMR Spectroscopic Investigation.

Diffusion-ordered NMR spectroscopy (DOSY) and nuclear Overhauser effect spectroscopy (NOESY) have been used to explore the diffusion and partitioning behavior of secondary surfactants added to suspensions of reverse micelles (RMs) containing either silver or gold nanoparticles (NPs), with an aim of advancing our understanding of the mechanism of metal NP extraction and/or surface functionalization with specific capping agents as performed during a microemulsion-based synthesis. We have coupled these NMR techniques with corresponding dynamic light scattering (DLS) measurements of RMs, with and without encapsulated metal NPs, upon addition of secondary surfactants. Using oleylamine (OAm), oleic acid (OA), dodecylamine (DDAm), and dodecanethiol (DDT), we show that all four secondary surfactants can rapidly diffuse into/out of the RM environment with their head groups in close proximity to the RM interior and encapsulated water molecules; however, surfactant molecules containing a terminal -NH2 or -COOH group undergo a persistent association with the molecules of the RMs, thus solubilizing and partially sequestering a portion of the total concentration of these secondary agents within the RM interface for a lengthened period of time (in relation to the time frame of the DOSY experiments) and slowing their rate of exchange with freely diffusing molecules in the bulk solvent. The extraction of Ag or Au NPs from RMs into organic phase was determined to be critically dependent on the type and concentration of secondary surfactant added to the system, with DDT proving to be most efficient for the extraction of Ag NPs, while OA was shown to be most efficient for Au NPs. Consideration of the results obtained from this particular combination of techniques has provided new knowledge with respect to dynamic metal NP-containing microemulsion systems.

Use of porous cellulose microcapsules for water treatment

Efficient extraction of Ag NPs and Au NPs using polyethyleneimine coated porous ethyl cellulose microcapsules.

3D Visualization of iron oxide nanoparticles in MRI of inflammatory model

Nanomedicine is becoming an extremely promising research area for healthcare. The visualization and quantification of nanoparticles (NPs) inside the organs of interest pose a significant challenge and therefore, novel image processing approaches are required for a better diagnosis. The purpose of this work was to develop a novel approach for better visualization and quantification of iron oxide NPs in three dimension (3D) high-resolution magnetic resonance (MR) images of an inflammatory model. The proposed procedure focuses on the extraction of NPs from the background surrounding it. It is applied on 2D and 3D images and is based on pre-processing and segmentation by automatic threshold to visualize the NPs inside the mouse calf using a control set of images of the same calf before injecting the NPs. The resulting visualization of the 3D distribution of iron oxide NPs inside the inflamed area of the calf has a potential in the advancement of NPs application in nanomedicine therapy and diagnosis.