The various properties of iron-platinum nanoparticles allow them to function in multiple ways. In standard conditions, FePt NPs exist in the face-centered cubic phase with a 3 to 10 nanometer diameter. However, once heat is added the structure becomes face-centered tetragonal.
For solid state applications FePt nanoparticles can be synthesised on a substrate by directly co-sputtering Fe and Pt.
FePt NPs are promising materials for ultra-high density magnetic recording media due to their high coercivity. Higher coercivity indicates the material cannot be demagnetized easily. After annealing at 700 °C, the film can have up to 14KOe coercivity compared to common hard drives that have 5KOe coercivity. Nanoparticles have also been grown with coercivities up to 37 kOe.
Due to their superparamagnetism and controllable shape, size, and surface, iron-platinum nanoparticles have great potential for advancing medicine in many fields, including imaging, pathogen detection, and targeted cancer therapy. The NPs can be conjugated with antibodies for tissue-specific delivery, providing a systematic way to customize for either technology. FePt NPs are compatible for CT scans because of their strong ability to absorb x-rays. FePt NPs also provide a non-toxic, more persistent alternative to iodinated molecules that are harmful to the kidney and survive in the body for only a short time.
The superparamagnetic properties of the nanoparticles and the systematic method for conjugating ligands to the FePt surface makes them viable vehicles for detection of pathogens such as gram-positive bacteria. Antibodies for the bacteria conjugated to the FePt NP bind to the bacteria and magnetic dipoles are used to detect the FePt NP-bacteria conjugate. By attaching peptides to the surface of the face-centered cubic FePt NPs, cytotoxic iron can be delivered to specific locations and taken up with high selectivity. A phospholipid coating of the FCC-FePt prevents Fe release. Once in the cell, the low pH of lysosome’s intracellular environments breaks down the phospholipid bilayer. Fe catalyzed decomposition of hydrogen peroxide into ROSs results in membrane lipid oxidation, damage to DNA and proteins, and tumor death.
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