4.7 Article

Influence of Polymer Shell Molecular Weight on Functionalized Iron Oxide Nanoparticles Morphology and In Vivo Biodistribution

期刊

PHARMACEUTICS
卷 14, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics14091877

关键词

magnetite nanoparticles; polyethylene glycol; morphology; in vivo; biodistribution

资金

  1. Romanian Ministry of Research National grants [PN 19060203, 543PED/2019]
  2. Romanian Ministry of Foreign Affairs [POSCCE-A2-O2.2.1-20131/Priority Axe 2, 638/12.03.2014, 1970]
  3. SMIS-CSNR [48652]

向作者/读者索取更多资源

Iron oxide nanoparticles (IONPs) have been widely used in biomedical applications due to their biocompatibility and magnetic properties. This study synthesized IONPs using a modified Massart method and evaluated their characteristics. The results showed that the functionalized IONPs had good biocompatibility and the ability to be cleared by the body.
Iron oxide nanoparticles (IONPs) have been extensively used in different biomedical applications due to their biocompatibility and magnetic properties. However, different functionalization approaches have been developed to improve their time-life in the systemic circulation. Here, we have synthesized IONPs using a modified Massart method and functionalized them in situ with polyethylene glycol with different molecular weights (20 K and 35 K). The resulting nanoparticles were characterized in terms of morphology, structure, and composition using transmission electron microscopy (TEM) and selected area electron diffraction (SAED). In vivo biodistribution was evaluated in Balb/c mice, the presence of IONP being evidenced through histopathological investigations. IONP morphological characterization showed a change in shape (from spherical to rhombic) and size with molecular weight, while structural characterization proved the obtaining of highly crystalline samples of spinel structured cubic face-centered magnetite. In vivo biodistribution in a mice model proved the biocompatibility of all of the IONP samples. All NPs were cleared through the liver, spleen, and lungs, while bare IONPs were also evidenced in kidneys.

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