by Ruiz, A, Salas, G, Calero, M, Hernández, Y, Villanueva, A, Herranz, F, Veintemillas-Verdaguer, S, Martínez, E, Barber, D F and Morales, M P
Abstract:
This study developed an approach for the synthesis of magnetic nanoparticles coated with three different polyethylene glycol (PEG)-derived molecules. The influence of the coating on different properties of the nanoparticles was studied. Magnetite nanoparticles (7 and 12 nm in diameter) were obtained via thermal decomposition of a coordination complex as an iron precursor to ensure nanoparticle homogeneity in size and shape. Particles were first coated with meso-2,3-dimercaptosuccinic acid by a ligand exchange process to remove oleic acid, followed by modification with three distinct short-chain PEG polymers, which were covalently bound to the nanoparticle surface via 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride activation of the carboxylic acids. In all cases, colloidal suspensions had hydrodynamic sizes 10nm) holds promise for biomedical applications.
Reference:
Short-chain PEG molecules strongly bound to magnetic nanoparticle for MRI long circulating agents. (Ruiz, A, Salas, G, Calero, M, Hernández, Y, Villanueva, A, Herranz, F, Veintemillas-Verdaguer, S, Martínez, E, Barber, D F and Morales, M P), In Acta biomaterialia, volume 9, 2013.
Bibtex Entry:
@article{Ruiz:2013ks,
author = {Ruiz, A and Salas, G and Calero, M and Hern{'a}ndez, Y and Villanueva, A and Herranz, F and Veintemillas-Verdaguer, S and Mart{'i}nez, E and Barber, D F and Morales, M P},
title = {{Short-chain PEG molecules strongly bound to magnetic nanoparticle for MRI long circulating agents.}},
journal = {Acta biomaterialia},
year = {2013},
volume = {9},
number = {5},
pages = {6421--6430},
month = may,
affiliation = {Departamento de Biomateriales y Materiales Bioinspirados, Instituto de Ciencia de Materiales de Madrid, CSIC, Madrid, Spain.},
doi = {10.1016/j.actbio.2012.12.032},
pmid = {23321305},
language = {English},
rating = {0},
date-added = {2015-01-08T16:02:57GMT},
date-modified = {2020-07-09T13:27:49GMT},
abstract = {This study developed an approach for the synthesis of magnetic nanoparticles coated with three different polyethylene glycol (PEG)-derived molecules. The influence of the coating on different properties of the nanoparticles was studied. Magnetite nanoparticles (7 and 12 nm in diameter) were obtained via thermal decomposition of a coordination complex as an iron precursor to ensure nanoparticle homogeneity in size and shape. Particles were first coated with meso-2,3-dimercaptosuccinic acid by a ligand exchange process to remove oleic acid, followed by modification with three distinct short-chain PEG polymers, which were covalently bound to the nanoparticle surface via 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride activation of the carboxylic acids. In all cases, colloidal suspensions had hydrodynamic sizes <100 nm and low surface charge, demonstrating the effect of PEG coating on the aggregation properties and steric stabilization of the magnetic nanoparticles. The internalization and biocompatibility of these materials in the HeLa human cervical carcinoma cell line were tested. Cells preincubated with PEG-coated iron nanoparticles were visualized outside the cells, and their biocompatibility at high Fe concentrations was demonstrated using a standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Finally, relaxivity parameters (r1 and r2) were used to evaluate the efficiency of suspensions as magnetic resonance imaging contrast agents; the r2 value was similar to that for Resovist and up to four times higher than that for Sinerem, probably due to the larger nanoparticle size. The time of residence in blood of the nanoparticles measured from the relaxivity values, and the Fe content in blood was doubled for rats and rabbits due to the PEG on the nanoparticle surface. The results suggest that this PEGylation strategy for large magnetic nanoparticles (>10nm) holds promise for biomedical applications.},
url = {http://linkinghub.elsevier.com/retrieve/pii/S1742706113000147},
uri = {url{papers3://publication/doi/10.1016/j.actbio.2012.12.032}}
}