scholarly journals A simple and efficient method for polymer coating of iron oxide nanoparticles

2020 ◽  
Vol 55 ◽  
pp. 101460 ◽  
Author(s):  
Ahmed Abushrida ◽  
Ibteisam Elhuni ◽  
Vincenzo Taresco ◽  
Luca Marciani ◽  
Snow Stolnik ◽  
...  
2015 ◽  
Vol 54 (23) ◽  
pp. 11236-11246 ◽  
Author(s):  
Hajo Meyer ◽  
Felix Winkler ◽  
Peter Kunz ◽  
Annette M. Schmidt ◽  
Alexandra Hamacher ◽  
...  

2015 ◽  
Vol 11 (1) ◽  
pp. 126-136 ◽  
Author(s):  
Lionel Maurizi ◽  
Anne-Laure Papa ◽  
Laure Dumont ◽  
Frédéric Bouyer ◽  
Paul Walker ◽  
...  

2018 ◽  
Vol 5 (12) ◽  
pp. 181369
Author(s):  
Adheesha N. Danthanarayana ◽  
Danushika C. Manatunga ◽  
Rohini M. De Silva ◽  
N. Vishvanath Chandrasekharan ◽  
K. M. Nalin De Silva

This study was carried out to develop a simple and efficient method to isolate DNA directly from biological samples using iron oxide nanoparticles (IONPs) functionalized with polyethyleneimine (PEI). IONPs were synthesized via co-precipitation method followed with direct attachment of branched PEI. Nanoparticles were characterized using STEM, FT-IR spectroscopy and XRD analysis. The binding capacity of synthesized PEI-IONPs for plasmid and genomic DNA was assessed using purified DNA samples. In order to elute bound DNA, elution conditions were optimized, changing pH, salt concentration and temperature. Synthesized PEI-IONPs were subjected to isolation of DNA from bacterial cell culture and from human blood. PCR and magnetofection of the enhanced green fluorescence protein (EGFP) were carried out to verify the downstream applications of isolated DNA. The results indicated that the synthesized nanoparticles were of 5–10 nm. The binding capacity of PEI-IONPs for plasmid DNA and genomic DNA were 5.4 and 8.4 µg mg −1 , respectively, which were even higher than the commercially available kits such as Mag-bind, MagJET and Magmax. The optimized condition for plasmid DNA elution was 0.1 M Tris HCl (pH 10.0), 1.5 M NaCl and 5% formamide, maintained at the temperature of 60°C. The optimized condition for genomic DNA elution was 0.1 M Tris HCl (pH 10.0), 1.5 M NaCl and 10% formamide, maintained at 60°C. PCR and magnetofection processes were successful. This study revealed that the magnetic separation of DNA using PEI-IONPs is a simple and efficient method for direct isolation of DNA from biological samples which can be then used in various downstream applications.


2016 ◽  
Vol 7 (45) ◽  
pp. 6875-6879 ◽  
Author(s):  
Bo Wang ◽  
Thomas Blin ◽  
Aleksandr Käkinen ◽  
Xinwei Ge ◽  
Emily H. Pilkington ◽  
...  

To provide a molecular insight for guiding polymer coating in surface science and nanotechnology, we examined the structural and stealth properties of brushed PEG- and phosphorylcholine-grafted iron oxide nanoparticles.


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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