scholarly journals Effect of Coordination Structure of Iron Ions on Iron Oxide Activities in Na2O–SiO2–FeO–Fe2O3 Melts

2019 ◽  
Vol 59 (10) ◽  
pp. 1744-1751
Author(s):  
Miyuki Hayashi ◽  
Kenya Horita ◽  
Rie Endo ◽  
Takashi Watanabe ◽  
Masahiro Susa
2004 ◽  
Vol 228 (1-4) ◽  
pp. 233-244 ◽  
Author(s):  
Shuji Matsuo ◽  
Nahomi Sakaguchi ◽  
Keiji Yamada ◽  
Taku Matsuo ◽  
Hisanobu Wakita

RSC Advances ◽  
2015 ◽  
Vol 5 (24) ◽  
pp. 18420-18428 ◽  
Author(s):  
A. B. Salunkhe ◽  
V. M. Khot ◽  
J. M. Ruso ◽  
S. I. Patil

Superparamagnetic iron oxide nanoparticles are synthesized through the co precipitation method by using the new generation base diisopropylamine (DIPA) which electrostatically complexes with the iron ions, reduces them and subsequently caps the nanoparticles.


2013 ◽  
Vol 41 (6) ◽  
pp. 1588-1592 ◽  
Author(s):  
Michaela C. Hohnholt ◽  
Ralf Dringen

Astrocytes are considered key regulators of the iron metabolism of the brain. These cells are able to rapidly accumulate iron ions and various iron-containing compounds, store iron efficiently in ferritin and also export iron. The present short review summarizes our current knowledge of the molecular mechanisms involved in the handling of iron by astrocytes. Cultured astrocytes efficiently take up iron as ferrous or ferric iron ions or as haem by specific iron transport proteins in their cell membrane. In addition, astrocytes accumulate large amounts of iron oxide nanoparticles by endocytotic mechanisms. Despite the rapid accumulation of high amounts of iron from various iron-containing sources, the viability of astrocytes is hardly affected. A rather slow liberation of iron from accumulated haem or iron oxide nanoparticles as well as the strong up-regulation of the synthesis of the iron storage protein ferritin are likely to contribute to the high resistance of astrocytes to iron toxicity. The efficient uptake of extracellular iron by cultured astrocytes as well as their strong up-regulation of ferritin after iron exposure also suggests that brain astrocytes deal well with an excess of iron and protect the brain against iron-mediated toxicity.


Nanoscale ◽  
2019 ◽  
Vol 11 (36) ◽  
pp. 16868-16878 ◽  
Author(s):  
Surya Narayanan ◽  
Emre Firlar ◽  
Md Golam Rasul ◽  
Tara Foroozan ◽  
Nasim Farajpour ◽  
...  

Ferritin is a protein that regulates the iron ions in humans by storing them in the form of iron oxides.


Author(s):  
H. Mori ◽  
Y. Murata ◽  
H. Yoneyama ◽  
H. Fujita

Recently, a new sort of nano-composites has been prepared by incorporating such fine particles as metal oxide microcrystallites and organic polymers into the interlayer space of montmorillonite. Owing to their extremely large specific surface area, the nano-composites are finding wide application[1∼3]. However, the topographic features of the microstructures have not been elucidated as yet In the present work, the microstructures of iron oxide-pillared montmorillonite have been investigated by high-resolution transmission electron microscopy.Iron oxide-pillared montmorillonite was prepared through the procedure essentially the same as that reported by Yamanaka et al. Firstly, 0.125 M aqueous solution of trinuclear acetato-hydroxo iron(III) nitrate, [Fe3(OCOCH3)7 OH.2H2O]NO3, was prepared and then the solution was mixed with an aqueous suspension of 1 wt% clay by continuously stirring at 308 K. The final volume ratio of the latter aqueous solution to the former was 0.4. The clay used was sodium montmorillonite (Kunimine Industrial Co.), having a cation exchange capacity of 100 mequiv/100g. The montmorillonite in the mixed suspension was then centrifuged, followed by washing with deionized water. The washed samples were spread on glass plates, air dried, and then annealed at 673 K for 72 ks in air. The resultant film products were approximately 20 μm in thickness and brown in color.


2018 ◽  
Vol 6 (10) ◽  
Author(s):  
Hosam Zaghloul ◽  
Doaa A. Shahin ◽  
Ibrahim El- Dosoky ◽  
Mahmoud E. El-awady ◽  
Fardous F. El-Senduny ◽  
...  

Antisense oligonucleotides (ASO) represent an attractive trend as specific targeting molecules but sustain poor cellular uptake meanwhile superparamagnetic iron oxide nanoparticles (SPIONs) offer stability of ASO and improved cellular uptake. In the present work we aimed to functionalize SPIONs with ASO targeting the mRNA of Cyclin B1 which represents a potential cancer target and to explore its anticancer activity. For that purpose, four different SPIONs-ASO conjugates, S-M (1–4), were designated depending on the sequence of ASO and constructed by crosslinking carboxylated SPIONs to amino labeled ASO. The impact of S-M (1–4) on the level of Cyclin B1, cell cycle, ROS and viability of the cells were assessed by flowcytometry. The results showed that S-M3 and S-M4 reduced the level of Cyclin B1 by 35 and 36%, respectively. As a consequence to downregulation of Cyclin B1, MCF7 cells were shown to be arrested at G2/M phase (60.7%). S-M (1–4) led to the induction of ROS formation in comparison to the untreated control cells. Furthermore, S-M (1–4) resulted in an increase in dead cells compared to the untreated cells and SPIONs-treated cells. In conclusion, targeting Cyclin B1 with ASO-coated SPIONs may represent a specific biocompatible anticancer strategy.


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