Iron Oxide Nanoparticles: Tunable Size Synthesis and Analysis in Terms of the Core–Shell Structure and Mixed Coercive Model

2017 ◽  
Vol 46 (4) ◽  
pp. 2533-2539 ◽  
Author(s):  
P. T. Phong ◽  
V. T. K. Oanh ◽  
T. D. Lam ◽  
N. X. Phuc ◽  
L. D. Tung ◽  
...  
2021 ◽  
Author(s):  
Nguyen Hoang Nam

Multifunctional silver nanoparticles have attracted widely due to their potential applications. Based on the properties of individual silver nanoparticles, such as plasmonic and antibacterial properties, silver nanoparticles can become multifunctional by surface modifications with various surfactants or they can be combined in core-shell and composite structures with the magnetic nanoparticles to form bifunctional nanoparticles. After reviewing the methods of synthesis and applications of silver nanoparticles, the chapter describes the synthesis and the properties of the new types of multifunctional silver nanomaterials based on the plasmonic behaviors of silver nanoparticles and the iron oxide Fe3O4 superparamagnetic nanoparticles. One type is a simple combination of silver nanoparticles and iron oxide nanoparticles in a silica matrix Fe3O4/Ag-4ATP@SiO2. Other types are the core-shell structured nanoparticles, where Fe3O4 nanoparticles play as the core and silver nanoparticles are the outer shell, so-called Fe3O4@SiO2-Ag and Fe3O4-Ag. In the Fe3O4@SiO2-Ag, silver nanoparticles are reduced on the surface of silica-coated magnetic core, while in Fe3O4-Ag, silver nanoparticles are directly reduced on the amino groups functionalized on the surface of magnetic nanoparticles without coating with silica. Both of types of the multifunctional silver nanoparticles show the plasmonic and magnetic properties similar as the individual silver and iron oxide nanoparticles. Finally, some applications of those multifunctional silver nanoparticles will be discussed.


2020 ◽  
Vol 10 (5) ◽  
pp. 6218-6225 ◽  

In this present study, Superparamagnetic Iron Oxide Nanoparticles (SPIONs) were produced using FeCl3 and FeCl2 which were reduced to iron oxides using NaOH and ammonia solution (chemical co-precipitation). These naked SPIONs were further fabricated to form drug laden core-shell for controlled drug release and delivery. The fabrication was achieved by subjugating the naked SPIONs for oleic acid functionalization, drug tagging (Itraconazole) and finally encapsulated with a microbial derived polyester namely Polyhydroxybutyrate (PHB). Every stage of fabrication was characterized by scanning electron microscopy (SEM). The core-shell produced was checked for drug release kinetics, antibacterial and antifungal activities. These synthesized core-shells were carrying the drug and showed a slow drug release profile. The antimicrobial studies against bacteria - Pseudomonas aeruginosa & Brevibacillus brevis and fungi - Candida albicans by diffusion method proved that the core-shells inhibited bacterial and fungal activity. Furthermore, the naked SPIONs was found to be a good contrasting agent in X-ray imaging.


Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 867
Author(s):  
Lin Guo ◽  
Zhu Mao ◽  
Sila Jin ◽  
Lin Zhu ◽  
Junqi Zhao ◽  
...  

Surface-enhanced Raman scattering (SERS) is a powerful tool in charge transfer (CT) process research. By analyzing the relative intensity of the characteristic bands in the bridging molecules, one can obtain detailed information about the CT between two materials. Herein, we synthesized a series of Au nanorods (NRs) with different length-to-diameter ratios (L/Ds) and used these Au NRs to prepare a series of core–shell structures with the same Cu2O thicknesses to form Au NR–4-mercaptobenzoic acid (MBA)@Cu2O core–shell structures. Surface plasmon resonance (SPR) absorption bands were adjusted by tuning the L/Ds of Au NR cores in these assemblies. SERS spectra of the core-shell structure were obtained under 633 and 785 nm laser excitations, and on the basis of the differences in the relative band strengths of these SERS spectra detected with the as-synthesized assemblies, we calculated the CT degree of the core–shell structure. We explored whether the Cu2O conduction band and valence band position and the SPR absorption band position together affect the CT process in the core–shell structure. In this work, we found that the specific surface area of the Au NRs could influence the CT process in Au NR–MBA@Cu2O core–shell structures, which has rarely been discussed before.


2021 ◽  
Author(s):  
Yu Qiao ◽  
Na Lv ◽  
Dong Li ◽  
Hongji Li ◽  
Xiangxin Xue ◽  
...  

Metastable Cu2O is an attractive material for the architecture design of integrated nanomaterials. In this context, Cu2O was used as the sacrificial agent to form the core-shell structure of Cu2O@HKUST-1...


RSC Advances ◽  
2016 ◽  
Vol 6 (94) ◽  
pp. 91463-91467 ◽  
Author(s):  
Peng Zhang ◽  
Shixun Bai ◽  
Shilan Chen ◽  
Dandan Li ◽  
Zhenfu Jia ◽  
...  

Well defined core–shell microspheres were prepared by surface-initiated atom transfer radical polymerization with pre-crosslinked polyacrylamide as the core and non-crosslinked polyacrylamide as the shell.


2016 ◽  
Vol 4 (35) ◽  
pp. 5831-5841 ◽  
Author(s):  
Min Liu ◽  
Lei Wu ◽  
Xi Zhu ◽  
Wei Shan ◽  
Lian Li ◽  
...  

The stability of the core–shell structure plays an important role in the nanoparticles ability to overcome both the mucus and epithelium absorption barrier.


2017 ◽  
Vol 10 (05) ◽  
pp. 1750056 ◽  
Author(s):  
Huiping Shao ◽  
Jiangcong Qi ◽  
Tao Lin ◽  
Yuling Zhou ◽  
Fucheng Yu

The core–shell structure composite magnetic nanoparticles (NPs), Fe3O4@chitosan@nimodipine (Fe3O4@CS@NMDP), were successfully synthesized by a chemical cross-linking method in this paper. NMDP is widely used for cardiovascular and cerebrovascular disease prevention and treatment, while CS is of biocompatibility. The composite particles were characterized by an X-ray diffractometer (XRD), a Fourier transform infrared spectroscopy (FT-IR), a transmission electron microscopy (TEM), a vibrating sample magnetometers (VSM) and a high performance liquid chromatography (HPLC). The results show that the size of the core–shell structure composite particles is ranging from 12[Formula: see text]nm to 20[Formula: see text]nm and the coating thickness of NMDP is about 2[Formula: see text]nm. The saturation magnetization of core–shell composite NPs is 46.7[Formula: see text]emu/g, which indicates a good potential application for treating cancer by magnetic target delivery. The release percentage of the NMDP can reach 57.6% in a short time of 20[Formula: see text]min in the PBS, and to 100% in a time of 60[Formula: see text]min, which indicates the availability of Fe3O4@CS@NMDP composite NPs for targeting delivery treatment.


2010 ◽  
Vol 46 (10) ◽  
pp. 1189-1197 ◽  
Author(s):  
B. I. Podlovchenko ◽  
T. D. Gladysheva ◽  
A. Yu. Filatov ◽  
L. V. Yashina

2014 ◽  
Vol 43 (24) ◽  
pp. 9283-9295 ◽  
Author(s):  
Xueqiang Qi ◽  
M. Rosa Axet ◽  
Karine Philippot ◽  
Pierre Lecante ◽  
Philippe Serp

The two-step synthesis of small ruthenium–platinum nanoparticles leads to the formation of a core–shell structure. The catalytic results provide supplementary evidence of the core–shell structure.


Soft Matter ◽  
2015 ◽  
Vol 11 (19) ◽  
pp. 3936-3945 ◽  
Author(s):  
Sang Min Lee ◽  
Young Chan Bae

Schematic depiction of a core–shell structure composed of the PMMA core and the PHEMA shell, and the influence of three co-solvents on the volume transition temperature of the core–shell gels in 1-propanol solution.


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