AI Article Synopsis

  • Amphiphilic surfactants like polysorbate 80 are used to create water-soluble magnetic nanoparticles (MFNPs) and modify their surfaces to tailor their properties.
  • The study confirmed the chemical modifications of polysorbate 80 using carboxyl and amine groups, resulting in three types of MFNPs that shared similar properties such as size and solubility.
  • Cationic MFNPs showed higher cytotoxicity and better cellular uptake in macrophages compared to anionic and non-ionic MFNPs, suggesting that surface charge is crucial for designing nanoparticles for medical uses.

Article Abstract

Amphiphilic surfactants have been used to disperse magnetic nanoparticles in biological media, because they exhibit a dual hydrophobic/hydrophilic affinity that facilitates the formation of a nanoemulsion, within which nanoparticle surfaces can be modified to achieve different physicochemical properties. For the investigation of the interactions of cells with charged magnetic nanoparticles in a biological medium, we selected the nanoemulsion method to prepare water-soluble magnetic nanoparticles using amphiphilic surfactant (polysorbate 80). The hydroxyl groups of polysorbate 80 were modified to carboxyl or amine groups. The chemical structures of carboxylated and aminated polysorbate 80 were confirmed, and water-soluble manganese ferrite nanoparticles (MFNPs) were synthesized with three types of polysorbate 80. Colloidal size, morphology, monodispersity, solubility and T2 relaxivity were found to be similar between the three types of MFNP. However, cationic MFNPs exhibited greater cytotoxicity in macrophages (RAW264.7 cells) and lower cellular membrane effective stiffness than anionic and non-ionic MFNPs. Moreover, cationic MFNPs exhibited large uptake efficiency for RAW264.7 cells compared with anionic or non-ionic MFNPs under the same conditions. Therefore, we propose that surface charge should be a key consideration factor in the design of magnetic nanoparticles for theragnostic applications.

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http://dx.doi.org/10.1088/0957-4484/23/50/505702DOI Listing

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