Chemical characterization and anti-hemolytic anemia potentials of tin nanoparticles synthesized by a green approach for bioremediation applications

The therapeutic properties of tin nanoparticles have been proved in recent years. One of their probable effects is anti-anemia. In this study, tin nanoparticles were synthesized and characterized in aqueous medium using Ziziphora clinopodioides Lam leaf aqueous extract as the reducing and stabilizing agent. We also assessed the antihemolytic anemia potential of tin nanoparticles (SnNPs) in an animal model of hemolytic anemia. Tin nanoparticles were characterized using many techniques including Fourier transform-infrared and UV-visible spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray spectrometry, and field emission-scanning electron microscopy (FE-SEM). FE-SEM images showed a uniform spherical morphology in size of 18.12 nm for the green synthesized nanoparticles. According to XRD analysis, SnNPs crystal size was17.94 nm. SnNPs had low cell viability dose-dependently against human umbilical vein endothelial cell line. in vivo design, induction of hemolytic anemia was done by phenylhydrazine in 40 mice. Tin nanoparticles significantly (p ≤ 0.01) reduced the weight and volume of liver and spleen and the concentration of pro-inflammatory cytokines, and increased the body weight, anti-inflammatory cytokines concentration, total platelet, WBC, neutrophil, lymphocyte, eosinophil, monocyte, and basophil counts, and red blood cell parameters compared to the untreated mice. For the biochemical parameters, SnNPs significantly (p ≤ 0.01) increased the concentrations of GPx, CAT, and SOD in serum, liver, and spleen and decreased the concentration of GR in serum, liver, and spleen, and also erythropoietin, ferritin, and ferrous in serum as compared to the anemic mice. The 2,2-diphenyl-1-picrylhydrazyl test showed similar antioxidant activities for SnNPs and butylated hydroxytoluene. The results demonstrate the excellent antihemolytic anemia, hematoprotective, cytotoxicity, and antioxidant potentials of SnNPs compared to other experimental groups.     

Iron (III) nanocomposites for enzyme-less biomimetic cathode: A promising material for use in biofuel cells

In this paper, we discuss the synthesis and electrochemical properties of a new material based on iron oxide nanoparticles stabilized with poly(diallyldimethylammonium chloride) (PDAC); this material can be used as a biomimetic cathode material for the reduction of H₂O₂ in biofuel cells. A metastable phase of iron oxide and iron hydroxide nanoparticles (PDAC–FeOOH/Fe₂O₃-NPs) was synthesized through a single procedure. On the basis of the Stokes–Einstein equation, colloidal particles (diameter: 20 nm) diffused at a considerably slow rate (D = 0.9 × 10^? 11 m s^? 1) as compared to conventional molecular redox systems. The quasi-reversible electrochemical process was attributed to the oxidation and reduction of Fe³⁺/Fe²⁺ from PDAC–FeOOH/Fe₂O₃-NPs; in a manner similar to redox enzymes, it acted as a pseudo-prosthetic group. Further, PDAC–FeOOH/Fe₂O₃-NPs was observed to have high electrocatalytic activity for H₂O₂ reduction along with a significant overpotential shift, ΔE = 0.68 V from ? 0.29 to 0.39 V, in the presence and absence of PDAC–FeOOH/Fe₂O₃-NPs. The abovementioned iron oxide nanoparticles are very promising as candidates for further research on biomimetic biofuel cells, suggesting two applications: the preparation of modified electrodes for direct use as cathodes and use as a supporting electrolyte together with H₂O₂.     

In vivo biodistribution,antioxidant and hemolysis tendency of superparamagnetic iron oxide nanoparticles – Potential anticancer agents

Ferromagnetic and superparamagnetic oxide nanoparticles are of particular attention because of their possible use in various fields ranging from bio-nanotechnology to spintronics. Detailed magnetic, dielectric and impedance investigations are crucial for the above-mentioned applications. This study deals with the exploration of various iron oxide phases under as-synthesized conditions by sol–gel method. pH of the sols is varied in the range of 1 to 11. X-ray diffraction (XRD) analysis indicate amorphous behavior for nanoparticles synthesized using pH 1 and 3. Nanoparticles synthesized using pH 2 and 4–6 exhibit hematite phase of iron oxide. Whereas structural transition to maghemite phase is observed for pH 7–8. Nanoparticles synthesized using high pH values, i.e. 9–11, exhibit structural transition towards magnetite phase of iron oxide. Hematite nanoparticles exhibit superparamagnetic and ferromagnetic hysteresis curves with saturation magnetization of ～ 24 emu/g and ～ 13–17 emu/g at pH 2 and pH 4–6, respectively. Maghemite nanoparticles exhibit superparamagnetic (pH 7) and ferromagnetic (pH 8) response with saturation magnetization of ～ 69 and ～ 42 emu/g, respectively. Fe₃O₄ nanoparticles exhibit superparamagnetic (pH 9–10) and ferromagnetic (pH 11) behavior with saturation magnetization of ～ 88, 87 and 52 emu/g, respectively. High grain boundary resistance contributed towards high dielectric constant of ～ 99, 109 and 154 (log f = 5.0) at pH 2, 7 and 9. Detailed impedance values indicate dominant role of grain boundaries in the conductivity of iron oxide nanoparticles. Superparamagnetic iron oxide (pH 9) exhibits strong antioxidant activity along with a very weak hemolytic response. The findings of cell lysis reveal that synthesized nanoparticles have a potential to combat dangerous cancer cells. Drug efficacy results show that after 120 min the encapsulation efficacy reaches a peak of ～ 83 % using curcumin, a naturally existing drug. In vivo biodistribution of nanoparticles was studied in Rabbit model. Synthesized nanoparticles are labelled using Technetium-99 m. Whereas, labeling efficacy and stability was examined using =nstant thin layer chromatography (ITLC) process. In vitro and in vivo results suggest potential anti-cancer applications of as-synthesized superparamagnetic nanoparticles.     

Ultrasensitive determination of serum albumin using resonance light scattering based on ZnS-polyacrylic acid nanoparticles

ZnS-polyacrylic acid (ZnS-PAA) was prepared by an in situ polymerization method using nano-ZnS as core in the presence of acrylic acid (AA), and ZnS-PAA nanoparticles was characterized by ultraviolet spectrometry (UV) and transmission electron microscopy (TEM). Based on the significant increase of the resonance light scattering (RLS) intensity with the interaction between nanoparticles and serum albumin, RLS method was developed for the sensitive determination of serum albumin (BSA and HSA). Under optimum conditions, the change of the intensity (ΔI) of the RLS spectra at λ = 392 nm was linearly proportional to the concentration of BSA and HSA. The linear range was 1–100 ng mL^?1 for HSA and 1–120 ng mL^?1 for BSA, and the limit of detection (LOD) was 0.4 ng mL^?1 for HSA and 0.5 ng mL^?1 for BSA. This method proved to be very sensitive, rapid, simple and tolerant of most interfering substances.     

Microstructure changes to iron nanoparticles during discharge/charge cycles

Iron nanoparticles that were synthesized by chemical reduction were used as the active material at the electrode, followed by measurement of their capacity during discharge/charge cycles. The discharge capacity of the first cycle was extremely high, 510 mAh/g-Fe, at a current density of 200 mA/g-Fe, indicating a marked increase in the capacity and the output current of iron electrodes when nanoparticles of iron, instead of micron-sized particles were used as the active materials. However, this capacity deteriorated rapidly during the discharge/charge cycles, while the size of iron nanoparticles increased, suggesting that the dissolution and re-crystallization of iron could have occurred during these cycles. A good correlation was found between the capacities and the surface areas of iron nanoparticles following each cycle. Our result further demonstrated that the capacity depends only on the surface area of iron particles, varying by 30 mAh with every 1 m² of iron.     

Application of natural compounds–based gold nanoparticles for the treatment of hemolytic anemia in an anemic mouse model: Formulation of a novel drug from relationship between the nanotechnology and hematology sciences

From time immemorial, people have tried to treat several diseases using natural compounds, including plants. Recently, researchers proposed that plants and herbal nanoparticles possess many remedial potentials. The results of this study confirmed the ability of an aqueous extract of Allium eriophyllum Boiss leaf grown under in vitro conditions for the biosynthesis of gold nanoparticles (AuNPs) and also revealed the anti-hemolytic anemia activity of AuNPs in an anemic rodent model. These nanoparticles were characterized using Fourier-transform infrared spectroscopy (FT-IR) spectroscopy, ultraviolet–visible spectroscopy, X-ray diffraction, field-emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). TEM and FE-SEM images showed the biosynthesized nanoparticles as having a uniform spherical morphology and diameters in the range of 5–30 nm. In vivo design, the induction of hemolytic anemia, was done using phenylhydrazine in 40 mice. Then, the mice were randomly divided into five groups: HAuCl₄, A. eriophyllum, AuNPs, untreated, and control. AuNPs significantly (p ≤ 0.01) decreased the concentration of glucocorticoid receptors in the serum, liver, and spleen, and also alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transferase, total and conjugated bilirubin, cholesterol, triglyceride, low-density lipoprotein, urea, creatinine, ferrous, ferritin, and erythropoietin in the serum increased the concentrations of superoxide dismutase, catalase, and glutathione peroxidase (GPx) in the serum, liver, and spleen and also total protein, high-density lipoprotein, and albumin in serum in the control mice as compared to the anemic mice. Also, AuNPs significantly (p ≤ 0.01) increased the body weight; anti-inflammatory cytokine (IL4, IL5, IL10, IL13, and IFNα) concentration; and the total platelet, white blood cells, lymphocyte, neutrophil, monocyte, eosinophil, and basophil counts and red blood cell parameters but decreased the weight and volume of the liver and spleen and their subcompartments and decreased the concentration of pro-inflammatory cytokines (IL1, IL6, IL12, IL18, IFNY, and TNFα) compared to the untreated mice. In vitro design, using 2,2-diphenyl-1-picrylhydrazyl test, revealed similar antioxidant potentials for A. eriophyllum, AuNPs, and butylated hydroxytoluene. In addition, AuNPs were similar to A. eriophyllum and had a high cell viability dose dependently against the human umbilical vein endothelial cell line. In conclusion, the results of the chemical characterization confirm that the leaves of A. eriophyllum can be used to produce AuNPs with a remarkable amount of anti-hemolytic anemia property.     

Extraction and preconcentration of trace levels of cobalt using functionalized magnetic nanoparticles in a sequential injection lab-on-valve system with detection by electrothermal atomic absorption spectrometry

A new approach to performing extraction and preconcentration employing functionalized magnetic nanoparticles for the determination of trace metals is presented. Alumina-coated iron oxide nanoparticles were synthesized and used as the solid support. The nanoparticles were functionalized with sodium dodecyl sulfate and used as adsorbents for solid phase extraction of the analyte. Extraction, elution, and detection procedures were performed sequentially in the sequential injection lab-on-valve (SI-LOV) system followed by electrothermal atomic absorption spectrometry (ETAAS). Mixtures of hydrophobic analytes were successfully extracted from solution using the synthesized magnetic adsorbents. The potential use of the established scheme was demonstrated by taking cobalt as a model analyte. Under the optimal conditions, the calibration curve showed an excellent linearity in the concentration range of 0.01–5 μg L^?1, and the relative standard deviation was 2.8% at the 0.5 μg L^?1 level (n = 11). The limit of detection was 6 ng L^?1 with a sampling frequency of 18 h^?1. The present method has been successfully applied to cobalt determination in water samples and two certified reference materials.     

Green biosynthesis of silver nanoparticles using Torreya nucifera and their antibacterial activity

Silver nanoparticles were biosynthesized with the aid of a novel and eco-friendly biological material Torreya nucifera. Temperature and extract concentration were found to influence the size and shape of the biosynthesized silver nanoparticles. Morphological images of biosynthesized nanomaterials revealed that the particles are in spherical shape and size ranging between 10 and 125 nm. Crystalline nature of nanoparticles in face centered cubic (fcc) structure was ensured by diffraction pattern peaks corresponding to (1 1 1), (2 0 0), (2 2 0) and (3 1 1) planes. Characterization of the biosynthesized nanoparticles was performed by the X-ray diffraction and Fourier Transform Infrared spectroscopy analyses. FT-IR analysis indicates that nanoparticles are bound to proteins through amine groups of the aminoacid. Furthermore the biosynthesized nanoparticles were found to be highly effective against Salmonella typhimurium bacterium, which validates its potential applications as antibacterial agents in drinking water treatment and in food packagings.     

Evaluation of the safety and antioxidant activities of Crocus sativus and Propolis ethanolic extracts

The possible toxicological effects and in vitro antioxidant activity of the ethanolic extracts of Crocus sativus and Propolis were investigated. Both extracts did not cause any mortalities or signs of toxicity in mice when administered orally at doses up to 5 g/kg b.wt. In the sub-chronic study; the tested extracts did not produce any significant change in liver and kidney functions of rats, following oral administration for 8 successive weeks at doses of 500 mg/kg b.wt. of each. Propolis showed remarkable in vitro antioxidant activity at concentrations of (40–100 mg/ml). In contrast, the ethanolic extract of C. sativus ethanolic extract showed weak antioxidant activity in concentrations of (1–10 mg/ml) while at concentrations of (20–100 mg/ml) failed to exhibit any antioxidant activity. It was concluded that: both extracts were non-toxic, as they did not cause any mortalities or signs of toxicity in mice when administered orally at doses up to 5 g/kg b.wt. Daily oral administration of C. sativus, Propolis ethanolic extracts alone or in combination for 8 successive weeks to rats was quiet safe and didn't cause any toxic changes in liver and kidney. Antioxidant study showed that Propolis ethanolic extract was a more potent antioxidant than C. sativus extract.     

Size-controllable synthesis of spherical ZnO nanoparticles: Size- and concentration-dependent resonant light scattering

A new and simple direct precipitation method assisted with ultrasonic agitation was proposed for the preparation of spherical ZnO nanoparticles. The size of the ZnO nanoparticles, 10 nm to 85 nm, was tuned through controlling the calcination temperature and changing the ratio of the reactants. The resonant light scattering (RLS) of the ZnO nanoparticles dispersed/suspended in aqueous solution of Triton X-100 was studied under room temperature. It was found that the ZnO nanoparticles of different size or concentration all have a characteristic RLS peak at 387 nm. Under optimal conditions, the RLS intensity was proportional to the ZnO concentration in the range of 7.3 × 10^?8–1 × 10^?4 mol L^?1, while the cubic root of the RLS intensity was found to be proportional to the size of ZnO nanoparticles. Further, the quantitative relationship of the size of the ZnO nanoparticles versus the calcination temperature was derived, and this could be used to forecast/control the nano-size in the nano-ZnO preparation.     

Synthesis,characterization and magnetic properties of γ-Fe2O3 nanoparticles via a non-aqueous medium

Acicular shaped γ-Fe₂O₃ nanoparticles (major axis: 17±2 nm; minor axis: 1.7±1 nm) have been prepared using lauric acid as a non-aqueous medium. The products were investigated by IR, TG-DTA, XRD, Raman, SEM, TEM and magnetization measurements. For the preparation of pure γ-Fe₂O₃ nanoparticles, the suitable condition of the molar ratio of lauric acid to iron nitrate is set 2:1 and the appropriate temperature lies in the range 573–673 K. Besides, either pure α-Fe₂O₃ or a mixture of γ-Fe₂O₃ and α-Fe₂O₃ can also be obtained with the change of the molar ratio of lauric acid to iron nitrate. The experimental results indicate that the particle sizes, thermal stability and magnetic properties of the iron oxide strongly depend on the conditions in the preparation.     

Nanoencapsulation and characterization of Albizia chinensis isolated antioxidant quercitrin on PLA nanoparticles

The plant isolated antioxidant quercitrin has been encapsulated on poly-d,l-lactide (PLA) nanoparticles by solvent evaporation method to improve the solubility, permeability and stability of this molecule. The size of quercitrin-PLA nanoparticles is 250 ± 68 nm whereas that PLA nanoparticles is 195 ± 55 nm. The encapsulation efficiency of nanoencapsulated quercitrin evaluated by HPLC and antioxidant assay is 40%. The in vitro release kinetics of quercitrin under physiological condition reveals initial burst release followed by sustained release. Less fluorescence quenching is observed with equimolar concentration of PLA encapsulated quercitrin than free quercitrin. The presence of quercitrin specific peaks on FTIR of five times washed quercitrin loaded PLA nanoparticles provides an extra evidence for the encapsulation of quercitrin into PLA nanoparticles. These properties of quercitrin nanomedicine provide a new potential for the use of such less useful highly active antioxidant molecule towards the development of better therapeutic for intestinal anti-inflammatory effect and nutraceutical compounds.     

Bioinspired synthesis of pure massicot phase lead oxide nanoparticles and assessment of their biocompatibility,cytotoxicity and in-vitro biological properties

Green and ecofriendly route for biosynthesis of lead oxide nanoparticles has been successfully demonstrated using aqueous leaf extracts of Sageretia thea (Osbeck.). Biosynthesized PbO (∼27 nm) nanoparticles were extensively characterized using XRD, FTIR, Raman, EDS etc. Morphology was studied through HR-TEM/SEM. As synthesized nanoparticles were investigated for their iv-vitro biological properties. Antibacterial activities revealed enhancement upon modulation by UV in a concentration dependent manner. Pseudomonas aeruginosa was found to be the most resistant strain (MIC = 250 µg/mL and MIC^uv = 31.25 µg/ml). MTT cytotoxicity on leishmania promastigotes and amastigotes revealed significant inhibition as indicated by their IC₅₀ values of 14.7 µg/mL and 11.95 µg/m respectively. Cytotoxicity was also confirmed using brine shrimp lethality (IC₅₀ = 27.7 µg/mL). Bio-compatibility evaluation indicated cytotoxicity to freshly isolated human macrophages (IC₅₀ = 57.1 µg/mL). Insignificant alpha-amylase inhibition and moderate protein kinase inhibition was revealed. Antioxidant activities indicated free radical scavenging activity (58 ± 2.45) at 200 µg/mL. Moderate total reducing power and total antioxidant activity was also indicated. Overall, we conclude lead oxide as a potential candidate for biological applications, however further studies are recommended on their in vitro and in vivo cytotoxicity.     

Potent antiviral effect of green synthesis silver nanoparticles on Newcastle disease virus

Newcastle disease virus (NDV) causes serious infectious diseases in birds, affecting poultry production. In addition to adverse side effects, almost all conventional drugs targeting viral proteins have drug resistance mutations. This study aimed to evaluate the antiviral activity of green silver nanoparticles using green tea leaf extract as a new strategy to control NDV in ovo. The Log embryo infective dose₅₀ (EID₅₀) virucidal reduction was used to measure the antiviral activity of silver nanoparticles against NDV. The treatment of Vero cells with the silver nanoparticles (AgNPs) at a noncytotoxic concentration significantly therapeutic value by inhibiting NDV entry and reduced viral replication, which led to a great reduction in the viral titer in ovo. In conclusion, silver nanoparticles are effective as a therapeutic antiviral agent against NDV and inhibit microbial resistance by making it difficult for the microbe to adapt.     

Green synthesis of plant-stabilized Au nanoparticles for the treatment of gastric carcinoma

In this study, gold nanoparticles (AuNPs) were green synthesized using plant extract. The obtained nanoparticles (Au NPs) were characterized by advanced physical and chemical techniques like TEM, FTIR, UV–vis, SEM, XRD and EDX. SEM image displayed the quasi-spherical shaped nanoparticles of mean diameter 20–50 nm. All the particles were of uniform shape and texture. From the XRD pattern, four distinct diffraction peaks at 38.2°, 44.2°, 64.7° and 77.4° are indexed as (1 1 1), (2 0 0), (2 2 0) and (3 1 1) planes of fcc metallic gold. The in vitro cytotoxic and anti-gastric carcinoma effects of biologically synthesized Au NPs against cancer cell lines were assessed. The IC₅₀ of the Au NPs were 192, 149, 76 and 85 µg/mL against NCI-N87, MKN45, GC1401 and GC1436 gastric cancer cell lines. The anti-gastric carcinoma properties of the Au NPs could significantly remove the cancer cell lines in a time and concentration-dependent manner. So, the findings of the recent research show that biologically synthesized Au NPs might be used to cure cancer.     

Mesoporous Fe2O3 nanoparticles as high performance anode materials for lithium-ion batteries

This work introduces an effective, inexpensive, and large-scale production approach to the synthesis of Fe₂O₃ nanoparticles with a favorable configuration that 5 nm iron oxide domains in diameter assembled into a mesoporous network. The phase structure, morphology, and pore nature were characterized systematically. When used as anode materials for lithium-ion batteries, the mesoporous Fe₂O₃ nanoparticles exhibit excellent cycling performance (1009 mA h g^− 1 at 100 mA g^− 1 up to 230 cycles) and rate capability (reversible charging capacity of 420 mA h g^− 1 at 1000 mA g^− 1 during 230 cycles). This research suggests that the mesoporous Fe₂O₃ nanoparticles could be suitable as a high rate performance anode material for lithium-ion batteries.     

Improving the cycleability of Si anodes by covalently grafting with 4-carboxyphenyl groups

In this study, the lithium storage capacity of Si nanoparticles is significantly enhanced by grafting with 4-carboxyphenyl groups via diazonium salts. The modified Si anodes exhibit reversible capacities of 1173 and 527 mA h g^?1 at the 1st and 50th cycle, while those of the bare Si electrodes are only 56 and 62 mA h g^?1, respectively. The improved electrochemical performance is supposed to arise from the formation of a robust and flexible solid electrolyte interface on the surfaces of the modified Si nanoparticles.     

Surface-enhanced Raman studies of bradykinin using colloidal gold

In this paper, bradykinin (BK), an endogenous peptide hormone, which is involved in a number of physiological and pathophysiological processes was deposited onto the colloidal Au nanoparticles. The surface-enhanced Raman spectroscopy (SERS) was used to determine the adsorption mode of BK under different environmental conditions, including: excitation wavelengths (514.5 nm and 785.0 nm), pH of aqueous sol solutions (from pH = 3 to pH = 11), and size of the colloidal nanoparticles (10, 20, and 50 nm). The metal surface plasmon of the colloidal suspended Au nanoparticles was examined by ultraviolet-visible (UV–vis) spectroscopy. The results showed that the C-terminal part of BK plays a crucial role in the adsorption process onto the colloidal suspended Au particles. The Phe^5/8 and Arg⁹ residues of BK mainly participate in the interactions with the colloidal Au nanoparticles. At acidic pH of the solution (pH = 3), the BK COO⁻ terminal group through the both oxygen atoms strongly binds to the Au nanoparticles. The Phe⁵/Phe⁸ rings adopt tilted orientation with respect to the colloidal Au nanoparticles with diameters of 10 and 20 nm. As the particle size increases to 50 nm, the flat orientation of the Phe ring(s) with respect to the Au nanoparticles is observed.     

Semi-elastic core-shell nanoparticles enhanced the oral bioavailability of peptide drugs

The rigidity of nanoparticles was newly reported to influence their oral delivery. Semi-elastic nanoparticles can enhance the penetration in mucus and uptake by epithelial cells. However, it is still challenging and unclear that the semi-elastic core-shell nanoparticles can enhance the oral bioavailability of peptide drugs. This study was for the first time to validate the semi-elastic core-shell poly(lactic-co-glycolic acid) (PLGA)-lipid nanoparticles (LNPs) as the carrier of the oral peptide drug. The antihypertensive peptide Val-Leu-Pro-Val-Pro (VP5) loaded LNPs (VP5-LNPs) were prepared by a modified thin-film ultrasonic dispersion method. Uptake experiment was performed in Caco-2 and HT-29 cells and monitored by high content screening (HCS) and flow cytometric (FCM). Pharmacokinetics of VP5-LNPs was carried out in Sprague-Dawley (SD) rats and analyzed by DAS 2.0. The optimal VP5-LNPs had an average particle size of 247.3 ± 3.8 nm, zeta potential of −6.57 ± 0.45 mV and excellent entrapment efficiency (EE) of 89.88% ± 1.23%. Transmission electron microscope (TEM) and Differential scanning calorimeter (DSC) further confirmed the core-shell structure. VP5-LNPs could increase the cellular uptake in vitro and have a 2.55-fold increase in AUC0-72 h, indicating a great promotion of the oral bioavailability. The semi-elastic LNPs remarkably improved the oral availability of peptide and could be a promising oral peptide delivery system for peptide drugs in the future.     

Embedding of Al nanoparticle in Al2O3 matrix by electron beam

Embedding structures of a metal nanoparticle in an oxide matrix were first achieved by electron beam irradiation. In the system of Al/α-Al₂O₃. Al nanoparticles derived from θ-Al₂O₃ migrated and embedded in α-Al₂O₃ matrix having epitaxy relation, {1 1 2̄ 0}α-Al₂O₃//{2 0 0} Al. The driving force of the embedding is momentum transfer from electrons or ions to Al atoms of nanoparticles in the pole piece of transmission electron microscopy.