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Aspartic Acid Stabilized Iron Oxide Nanoparticles for Biomedical Applications
| Content Provider | MDPI |
|---|---|
| Author | Mihaela, Răcuciu Olga, Drăghici Florin, Brînză Dorina, E. Creangă Barbu-Tudoran, Lucian Oancea, Simona Morosanu, Cezarina Grigoras, Marian |
| Copyright Year | 2022 |
| Description | Aspartic acid stabilized iron oxide nanoparticles (A-IONPs) with globular shape and narrow size distribution were prepared by the co-precipitation method in aqueous medium. A quantum-mechanical approach to aspartic acid optimized structure displayed negative charged sites, relatively high dipole moment, and hydrophilicity, which recommended it for interaction with iron cations and surrounding water electrical dipoles. A-IONPs were characterized by TEM, XRD, ATR-FTIR, EDS, DSC, TG, DLS, NTA, and VSM techniques. Theoretical study carried out by applying Hartree-Fock and density functional algorithms suggested that some aspartic acid properties related to the interaction can develop with nanoparticles and water molecules. The results of experimental investigation showed that the mean value of particle physical diameters was 9.17 ± 2.2 nm according to TEM image analysis, the crystallite size was about 8.9 nm according to XRD data, while the magnetic diameter was about 8.8 nm, as was determined from VSM data interpretation with Langevin’s theory. The A-IONP suspension was characterized by zeta-potential of about −11.7 mV, while the NTA investigation revealed a hydrodynamic diameter of 153.9 nm. These results recommend the A-IONP suspension for biomedical applications. |
| Starting Page | 1151 |
| e-ISSN | 20794991 |
| DOI | 10.3390/nano12071151 |
| Journal | Nanomaterials |
| Issue Number | 7 |
| Volume Number | 12 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2022-03-30 |
| Access Restriction | Open |
| Subject Keyword | Nanomaterials Iron Oxide Nanoparticles Nanoparticles Synthesis L-aspartic Acid Nanoparticles Size Physical and Chemical Characterization |
| Content Type | Text |
| Resource Type | Article |