Poly(N,N-dimethylacrylamide)-coated maghemite nanoparticles for stem cell labeling
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19238690
DOI
10.1021/bc800373x
Knihovny.cz E-resources
- MeSH
- Acrylamides chemistry MeSH
- Staining and Labeling methods MeSH
- Rats MeSH
- Humans MeSH
- Magnetic Resonance Spectroscopy MeSH
- Magnetic Resonance Imaging MeSH
- Mesenchymal Stem Cells cytology metabolism ultrastructure MeSH
- Nanoparticles chemistry MeSH
- Scattering, Radiation MeSH
- Spectroscopy, Fourier Transform Infrared MeSH
- Microscopy, Electron, Transmission MeSH
- Cell Survival MeSH
- Gelatin metabolism MeSH
- Ferric Compounds chemical synthesis chemistry metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acrylamides MeSH
- ferric oxide MeSH Browser
- poly(N,N-dimethylacrylamide) MeSH Browser
- Gelatin MeSH
- Ferric Compounds MeSH
Maghemite (gamma-Fe2O3) nanoparticles were obtained by the coprecipitation of Fe(II) and Fe (III) salts with ammonium hydroxide followed by oxidation with sodium hypochlorite. Solution radical polymerization of N,N-dimethylacrylamide(DMAAm) in the presence of maghemite nanoparticles yielded poly(N,N-dimethylacrylamide)(PDMAAm)-coated maghemite nanoparticles. The presence of PDMAAm on the maghemite particle surface was confirmed by elemental analysis and ATR FTIR spectroscopy. Other methods of nanoparticle characterization involved scanning and transmission electron microscopy, atomic adsorption spectroscopy (AAS), and dynamic light scattering (DLS). The conversion of DMAAm during polymerization and the molecular weight of PDMAAmbound to maghemite were determined by using gas and size-exclusion chromatography, respectively. The effect of ionic 4,4'-azobis(4-cyanovaleric acid) (ACVA) initiator on nanoparticle morphology was elucidated. The nanoparticles exhibited long-term colloidal stability in water or physiological buffer. Rat and human bone marrow mesenchymal stem cells (MSCs) were labeled with uncoated and PDMAAm-coated maghemite nanoparticles and with Endorem as a control. Uptake of the nanoparticles was evaluated by Prussian Blue staining, transmission electron microscopy, T(2)-MR relaxometry, and iron content analysis. Significant differences in labeling efficiency were found for human and rat cells. PDMAAm-modified nanoparticles demonstrated a higher efficiency of intracellular uptake into human cells in comparison with that of dextran-modified (Endorem) and unmodified nanoparticles. In gelatin, even a small number of labeled cells changed the contrast in MR images. PDMAAmcoatednanoparticles provided the highest T(2) relaxivity of all the investigated particles. In vivo MR imaging ofPDMAAm-modified iron oxide-labeled rMSCs implanted in a rat brain confirmed their better resolution compared with Endorem-labeled cells.
References provided by Crossref.org
Photoacoustic Properties of Polypyrrole Nanoparticles
Influence of surface-modified maghemite nanoparticles on in vitro survival of human stem cells
The use of dopamine-hyaluronate associate-coated maghemite nanoparticles to label cells