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High quality Fe3O4 magnetic nanoparticles coated with gallic acid for drug delivery

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Thermochromism refers to the phenomenon where a material undergoes color changes under temperature changes. This change is usually caused by changes in the electronic or molecular structure of the material. Its application principle mainly involves t...

High quality Fe3O4 magnetic nanoparticles coated with gallic acid for drug delivery

  • July 7,2016.
      Background and methods: Magnetic Ferroferric Oxide nanoparticles were prepared using a sonochemical method under atmospheric conditions at a Fe2+ to Fe3+ molar ratio of 1:2. The iron oxide nanoparticles were subsequently coated with chitosan and gallic acid to produce a core-shell structure.
Magnetic properties



      Magnetic propertiesfe3o4 nanoparticles coated with chitosan and gallic acid were characterized by vibrating sample magnetometry. the hysteresis loops as a function of the magnetic field at room temperature. The magnetic parameters, including saturation magnetization and remnant magnetization, The saturation magnetization of the fe3o4 nanoparticles core-shelled by chitosan and gallic acid was about 26.074 emu/g, while the naked fe3o4 was about 29.091 emu/g. The decrease in saturation magnetization was most likely due to the existence of coated materials and impurities on the surface of the magnetic nanoparticles.45 According to the vibrating sample magnetometry results, the nanoparticles showed superparamagnetic behavior, ie, they did not retain any magnetism after removal of the magnetic field. High magnetization and super paramagnetic properties are highly sought after for biomedical applications because the larger magnetic particles form aggregates after exposure to a magnetic field.



      Results: X-ray diffraction demonstrated that the magnetic nanoparticles were pure Fe3O4 with a cubic inverse spinel structure. Transmission electron microscopy showed that the ferroferric Oxide nanoparticles were of spherical shape with a mean diameter of 11 nm, compared with 13 nm for the ferroferric Oxide-chitosan-gallic acid (FCG) nano carriers.


      Conclusion: The magnetic nano carrier enhanced the thermal stability of the drug, gallic acid. Release of the active drug from the FCG nano carrier was found to occur in a controlled manner. The gallic acid and FCG nanoparticles were not toxic in a normal human fibroblast (3T3) line, and anticancer activity was higher in HT29 than MCF7 cell lines.




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