scholarly journals Biosynthesized Iron Oxide Nanoparticles (Fe3O4 NPs) Mitigate Arsenic Toxicity in Rice Seedlings

Toxics ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 2
Author(s):  
Sehresh Khan ◽  
Nazneen Akhtar ◽  
Shafiq Ur Rehman ◽  
Shaukat Shujah ◽  
Eui Shik Rha ◽  
...  

Arsenic (As) contamination has emerged as a serious public health concern worldwide because of its accumulation and mobility through the food chain. Therefore, the current study was planned to check the effect of Bacillus subtilis-synthesized iron oxide nano particles (Fe3O4 NP) on rice (Oryza Sativa L.) growth against arsenic stress (0, 5, 10 and 15 ppm). Iron oxide nanoparticles were extracellular synthesized from Bacillus subtilis with a desired shape and size. The formations of nanoparticles were differentiated through UV-Visible Spectroscopy, FTIR, XRD and SEM. The UV-Visible spectroscopy of Bacillus subtilis-synthesized nanoparticles showed that the iron oxide surface plasmon band occurs at 268 nm. FTIR results revealed that different functional groups (aldehyde, alkene, alcohol and phenol) were present on the surface of nanoparticles. The SEM image showed that particles were spherical in shape with an average size of 67.28 nm. Arsenic toxicity was observed in seed germination and young seedling stage. The arsenic application significantly reduced seed germination (35%), root and shoots length (1.25 and 2.00 cm), shoot/root ratio (0.289), fresh root and shoots weight (0.205 and 0.260 g), dry root and shoots weight (6.55 and 6.75 g), dry matter percentage of shoot (12.67) and root (14.91) as compared to control. Bacillus subtilis-synthesized Fe3O4 NPs treatments (5 ppm) remarkably increased the germination (65%), root and shoot length (2 and 3.45 cm), shoot/root ratio (1.24) fresh root and shoot weight (0.335 and 0.275 mg), dry root and shoot weight (11.75 and 10.6 mg) and dry matter percentage of shoot (10.40) and root (18.37). Results revealed that the application of Fe3O4 NPs alleviated the arsenic stress and enhanced the plant growth. This study suggests that Bacillus subtilus-synthesized iron oxide nanoparticles can be used as nano-adsorbents in reducing arsenic toxicity in rice plants.

2019 ◽  
Vol 9 (2) ◽  
pp. 166-172
Author(s):  
Ahmed A.G. El-Shahawy ◽  
Gamal Elghnam ◽  
Alsayed A.M. Alsherbini

Background:Gold and Iron Oxide nanoparticles NPs play as nanocarriers for a specific drug delivery and contrast agents. Intercellular uptake of these nanoparticles and targeting to individual cell and sub-cellular compartment is essential.Objective:The aim of the current study is to evaluate the intracellular uptake of these NPs to specific tumor cells in vitro conjugated with folic acid with a goal of enhancing the efficiency of specific targeting to tumor cells.Methods:We synthesized the nanoparticles by a chemical method and characterized by UV-Visible, FTIR, XRD, and TEM.Results & Conclusion:The results revealed the conjugation of Gold and Iron Oxide nanoparticles with folic acid increased the intercellular uptake with high percent compared to non- conjugated nanoparticles.


2019 ◽  
Vol 31 (8) ◽  
pp. 1719-1723
Author(s):  
Nguyen Thi Thanh Thuy ◽  
Le Duc Anh ◽  
Nguyen Huu Tri ◽  
Cu Van Hoang ◽  
Nguyen Anh Nhut

The PEG-coated iron oxide nanoparticles (Fe3O4 NPs-PEG) was synthesized by coprecipitation and ultrasonication method. X-ray diffraction results exhibited that the average size of Fe3O4 NPs-PEG was 19.10 nm, which was further confirmed in TEM imaging. In addition, sonication time and curcumin concentration were studied to evaluate the efficiency of loading curcumin onto Fe3O4 NPs-PEG. Further, statistical optimization using response surface methodology (RSM) has shown curcumin concentration (0,01% w/v) and sonication time (21 min) for maximal curcumin loading (0.37 mg/g). Along with the magnetization studies, the immobilization of curcumin onto the Fe3O4 NPs-PEG was characterized by UV, FTIR and SEM. The results showed that the curcumin loaded PEG coated iron oxide nanoparticles could potentially be used for magnetically target drug delivery.


Author(s):  
BEENA JOSE ◽  
FEMY THOMAS

Objective: The objective of the present study is the synthesis of iron oxide nanoparticles using Annona muricata aqueous leaf extract, characterization of the synthesized nanoparticles and evaluation of the antibacterial, photocatalytic activity and cytotoxicity. Methods: The iron oxide nanoparticle was synthesized using Annona muricata aqueous leaf extract and the crystal structure of the iron oxide nanoparticle was determined by UV-Visible spectroscopy, Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR). The in vitro cytotoxicity of iron oxide nanoparticles was evaluated using Dalton’s lymphoma ascites cells and the antibacterial assay was conducted using agar well diffusion method. Results: The UV-Visible spectrum of iron oxide nanoparticle showed a maximum absorption peak at 265 nm. This is the XRD pattern of iron oxide nanoparticles exhibited a distinct peak at 26.029 (2θ), accounting for crystal plane (211). SEM images revealed that the synthesized iron oxide nanoparticles were aggregated as irregular sphere shapes with rough surfaces. TEM image reveals the size of the synthesized iron oxide nanoparticles are spherical in shape with an average size of 20 nm. Green synthesized iron oxide nanoparticles using Annona muricata leaf extract effectively degraded methylene blue dye. Conclusion: This study showed that the synthesized iron oxide nanoparticles using Annona muricata aqueous leaf extract exhibited pronounced antibacterial, anticancer and photocatatytic activity and can be used in the textile industry for the purification of water contaminated with carcinogenic textile dyes. It can also be used as an external antiseptic in the prevention and treatment of bacterial infections.


2017 ◽  
Vol 62 ◽  
pp. 231-240 ◽  
Author(s):  
Dinali Ranmadugala ◽  
Alireza Ebrahiminezhad ◽  
Merilyn Manley-Harris ◽  
Younes Ghasemi ◽  
Aydin Berenjian

2019 ◽  
Vol 57 (3A) ◽  
pp. 160
Author(s):  
Minh-Tri Nguyen-Le ◽  
Dinh Tien Dung Nguyen ◽  
Sophia Rich ◽  
Ngoc Tram Nguyen ◽  
Cuu Khoa Nguyen ◽  
...  

Advances in nanotechnology in recent years has led to a number of diverse applications of nanomaterials. Magnetic iron oxide nanoparticles (Fe3O4 NPs), a representative of magnetic nanomaterials, has gained much attention of many researchers all over the world due to their unique properties such as superparamagnetism, biocompatibility and high magnetic saturation. With such properties, Fe3O4 NPs can be exploited in many fields, particularly biomedicine related fields such as cellular therapy, tissue repair, drug delivery, magnetic resonance imaging, hyperthermia and magnetofection. However, owing to their self-aggregation of Fe3O4 NPs, it is necessary to coat Fe3O4 NPs with a stable and biocompatible silica layer. Therefore, in this report, Fe3O4 NPs were synthesized via a co-precipitation method using iron (II)/ iron (III) chloride, ammonia and trisodium citrate. Then, the silica layer was coated onto Fe3O4 NPs through the hydrolysis and condensation of tetraethyl orthosilicate (TEOS) in ethanol. The as-synthesized samples were charaterized with the infrared (IR) spectroscopy, X-ray diffraction (XRD) spectroscopy, thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), transmission electron microscopy (TEM) and dynamic light scattering (DLS). The results proved that silica was successfully coated on Fe3O4 NPs. The particle sizes measured by TEM were found to be about 12 nm in diameter for Fe3O4 NPs and 45 nm in diameter for silica coated Fe3O4 (SiO2@Fe3O4) NPs, while the dynamic diameters measured by DLS for Fe3O4 NPs and SiO2@Fe3O4 NPs were 15.7 and 65.8 nm, respectively. Both Fe3O4 NPs and SiO2@Fe3O4 NPs were superparamagnetic materials in which Fe3O4 NPs have higher magnetic saturation (45.8 emu/g) than the other (13.4 emu/g).This study examines the: ……...Advances in nanotechnology in recent years has led to a number of diverse applications of nanomaterials. Magnetic iron oxide nanoparticles (Fe3O4 NPs), a representative of magnetic nanomaterials, has gained much attention of many researchers all over the world due to their unique properties such as superparamagnetism, biocompatibility and high magnetic saturation. With such properties, Fe3O4 NPs can be exploited in many fields, particularly biomedicine related fields such as cellular therapy, tissue repair, drug delivery, magnetic resonance imaging, hyperthermia and magnetofection. However, owing to their self-aggregation of Fe3O4 NPs, it is necessary to coat Fe3O4 NPs with a stable and biocompatible silica layer. Therefore, in this report, Fe3O4 NPs were synthesized via a co-precipitation method using iron (II)/ iron (III) chloride, ammonia and trisodium citrate. Then, the silica layer was coated onto Fe3O4 NPs through the hydrolysis and condensation of tetraethyl orthosilicate (TEOS) in ethanol. The as-synthesized samples were charaterized with the infrared (IR) spectroscopy, X-ray diffraction (XRD) spectroscopy, thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), transmission electron microscopy (TEM) and dynamic light scattering (DLS). The results proved that silica was successfully coated on Fe3O4 NPs. The particle sizes measured by TEM were found to be about 12 nm in diameter for Fe3O4 NPs and 45 nm in diameter for silica coated Fe3O4 (SiO2@Fe3O4) NPs, while the dynamic diameters measured by DLS for Fe3O4 NPs and SiO2@Fe3O4 NPs were 15.7 and 65.8 nm, respectively. Both Fe3O4 NPs and SiO2@Fe3O4 NPs were superparamagnetic materials in which Fe3O4 NPs have higher magnetic saturation (45.8 emu/g) than the other (13.4 emu/g).


2020 ◽  
Vol 16 (1) ◽  
pp. 91-100
Author(s):  
Sadaf Batool ◽  
Zakir Hussain

Background: : Iron Oxide nanoparticles have enormous applications in environmental remediation and catalysis. The synthesis of such nanoparticles through a green approach provides a significant advantage due to the non-toxic nature of the ingredients involved. Method: : In the present work, Diospyros lotus fruit extract was used for the synthesis of iron oxide nanoparticles (NPs). The plant biomolecules were extracted employing two different solvents, i.e. water and methanol. The effect of both the extracts on the reduction of metal salt as well as on the shape and size of the produced NPs was investigated. Results:: UV-Visible spectroscopy confirmed the synthesis of iron oxide NPs, Fourier Transform Infrared (FTIR) spectrum depicted the presence of biomolecules on the surface of NPs as capping agents, X-ray Diffraction (XRD) diffractogram confirmed the crystalline structure of mixed iron oxide NPs and Scanning Electron Microscopy (SEM) images showed the spherical shape of NPs. The synthesized NPs were exploited to catalyze the degradation of methylene blue dye in the Fenton type catalytic reaction. The degradation reaction was monitored using UV-Visible spectroscopy, which indicated that the percent degradation increased from 15% (without iron oxide NPs) to 91% in the presence of organic extract prepared iron oxide NPs and to 81% in the presence of aqueous extract prepared iron oxide NPs. The effect of the concentration of methylene blue and iron oxide NPs on the degradation process was also investigated. Conclusion: : The results indicated the potential of synthesized nanoparticles to promote catalytic reactions involved in environmental remediation.


2021 ◽  
Vol 17 ◽  
Author(s):  
Zhibo Yu ◽  
Liang Jia ◽  
Jianzhi Zhu ◽  
Mingwu Shen ◽  
Jingchao Li ◽  
...  

Background: The highly sensitive and selective detection of Cr3+ is critical. Objective: We report the development of poly(γ-glutamic acid) (γ-PGA)-functionalized iron oxide nanoparticles (γ-PGA-Fe3O4 NPs) as a magnetic nanosensor for magnetic resonance (MR) detection of trivalent chromium (Cr3+) in aqueous solution. Methods: The γ-PGA-Fe3O4 NPs with a mean particle size of 7.3 nm, good colloidal stability and ultrahigh r2 relaxivity (326.8 mM−1s−1) were synthesized via a facile mild reduction approach in the presence of γ-PGA, and used for MR detection of Cr3+. Results: Upon exposure to Cr3+, the γ-PGA-Fe3O4 NPs aggregated into nanoclusters as verified by dynamic light scattering due to the coordination of Cr3+ with γ-PGA side chain carboxyl groups, resulting in the decrease in their transverse relaxation time. This MR signal change enables detection of Cr3+ in a concentration range of 0.4-1 nM. We also show that the γ-PGA-Fe3O4 NPs have an excellent selectivity toward Cr3+ and a high recovery percentage of 83.8% or above. Conclusion: This study thus demonstrates that the developed γ-PGA-Fe3O4 NPs may be used as a nanoprobe for MR sensing of Cr3+ in water environment.


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