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Poly(ethylene glycol)-block-poly(4-vinyl pyridine) as a versatile block copolymer to prepare nanoaggregates of superparamagnetic iron oxide nanoparticles
Author(s) -
Nuno Rocha,
Joana P. Mendes,
Luísa Durães,
Hajar Maleki,
António Portugal,
Carlos F. G. C. Geraldes,
Arménio C. Serra,
Jorge F. J. Coelho
Publication year - 2014
Publication title -
journal of materials chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 101
eISSN - 2050-7518
pISSN - 2050-750X
DOI - 10.1039/c3tb21454k
Subject(s) - copolymer , ethylene glycol , amphiphile , materials science , atom transfer radical polymerization , nanoparticle , superparamagnetism , ethylene oxide , polymer chemistry , aqueous solution , polymerization , pyridine , chemical engineering , nanotechnology , chemistry , organic chemistry , polymer , magnetization , physics , quantum mechanics , magnetic field , engineering , composite material
This work reports an efficient method for the preparation of aqueous dispersions of superparamagnetic iron oxide nanoparticles (SPIONs), involving the use of an amphiphilic block copolymer, poly(ethylene glycol)-block-poly(4-vinyl pyridine) (mPEG-b-P4VP). The iron oxide nanoparticles are easily and efficiently dispersed due to the strong direct interaction of the hydrophobic P4VP segments, through complexation with pyridine units of the copolymer. Well-defined block copolymers, having different compositions and molecular weights, were prepared by atom transfer radical polymerization (ATRP). The aqueous self-assembly behavior of each system has been compared based on the method of preparation. The results revealed that the addition of ionic species has a significant effect on the size and type of formed nanostructures, the magnitude of which is dependent on the block copolymers' molecular design. When similar self-assembly strategies were used in the presence of SPIONs, the same type of nanostructures was formed. The hybrid SPION nanoaggregates were investigated using NMR relaxometric techniques, whereby high r 2 /r 1 relaxivity ratios were achieved, making these materials potentially efficient T 2 -weighted MRI contrast agents.

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