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Fe3O4 magnetic core coated by silver and functionalized with N-acetyl cysteine as novel nanoparticles in ferritin adsorption
A novel metal-chelate affinity matrix utilizing N -acetyl cysteine as a metal chelating agent was synthesized. For this, magnetic Fe 3 O 4 core was coated with silver by chemical reduction. Then, these magnetic silver nanoparticles were covered with N -acetyl cysteine, and Fe 3+ was chelated to this...
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Published in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2013-04, Vol.15 (4), Article 1564 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel metal-chelate affinity matrix utilizing
N
-acetyl cysteine as a metal chelating agent was synthesized. For this, magnetic Fe
3
O
4
core was coated with silver by chemical reduction. Then, these magnetic silver nanoparticles were covered with
N
-acetyl cysteine, and Fe
3+
was chelated to this modified magnetic silver nanoparticle. These magnetic nanoparticles were characterized by SEM, AFM, EDX, and ESR analysis. Synthesized nanoparticles were spherical and average size is found to be 69 nm. Fe
3+
chelated magnetic silver nanoparticles were used for the adsorption of ferritin from its aqueous solution. Optimum conditions for the ferritin adsorption experiments were performed at pH 6.0 phosphate buffer and 25 °C of medium temperature and the maximum ferritin adsorption capacity is found to be 89.57 mg/g nanoparticle. Ferritin adsorption onto magnetic silver nanoparticles was increased with increasing ferritin concentration while adsorption capacity was decreased with increasing ionic strength. Affinity of the magnetic silver nanoparticles to the ferritin molecule was shown with SPR analysis. It was also observed that the adsorption capacity of the magnetic silver nanoparticles was not significantly changed after the five adsorption/desorption cycles. |
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ISSN: | 1388-0764 1572-896X |
DOI: | 10.1007/s11051-013-1564-y |