Continuous Hydrothermal Preparation of Partially Substituted Perovskite Oxide Nanoparticles

2007 ◽  
Vol 36 (10) ◽  
pp. 1262-1263 ◽  
Author(s):  
Jinfeng Lu ◽  
Yukiya Hakuta ◽  
Hiromichi Hayashi ◽  
Tomotsugu Ohashi ◽  
Yasushi Hoshi ◽  
...  
Nanoscale ◽  
2021 ◽  
Author(s):  
Calum McDonald ◽  
Chengsheng Ni ◽  
Vladimir Švrček ◽  
Manuel Macias-Montero ◽  
Tamilselvan Velusamy ◽  
...  

We observe the extraction of carriers excited between two types of bands in the perovskite oxide, Sr-deficient strontium niobate (Sr0.9NbO3).


RSC Advances ◽  
2016 ◽  
Vol 6 (97) ◽  
pp. 94826-94832 ◽  
Author(s):  
Ankita Mathur ◽  
H. S. Kushwaha ◽  
Rahul Vaish ◽  
Aditi Halder

Perovskite oxide based materials have drawn considerable amount of attention as non-precious, non-noble cathode catalysts in oxygen reduction reactions for fuel cell and battery applications.


2019 ◽  
Vol 55 (79) ◽  
pp. 11880-11883 ◽  
Author(s):  
William Shepherd ◽  
Michael Wilms ◽  
Joel van Embden ◽  
Enrico Della Gaspera

A reliable synthesis for pure and doped BaSnO3 nanoparticles is presented, solving current irreproducibility issues affecting this emerging transparent conducting oxide.


2011 ◽  
Vol 196 (1) ◽  
pp. 65-72 ◽  
Author(s):  
M. Ali Haider ◽  
Aaron J. Capizzi ◽  
Mitsuhiro Murayama ◽  
Steven McIntosh

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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