| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1488251 | Materials Research Bulletin | 2014 | 6 Pages |
•The PEG and FA modified Mn3O4@SiO2 nanoparticles (Mn3O4@SiO2–FA) were prepared.•Mn3O4@SiO2–FA exhibited the good colloidal stability in the simulated biological medium.•Mn3O4@SiO2–FA showed the targeting ability to HeLa cells overexpressed the FA receptor.•The T1-weighted magnetic resonance (MR) imaging demonstrated the targeting ability of Mn3O4@SiO2–FA in vivo tumor.
The monodisperse silica-coated manganese oxide nanoparticles (Mn3O4@SiO2 NPs) were synthesized via the high temperature pyrolysis approach and were aminated through silanization. The amine-functionalized Mn3O4 NPs enabled the covalent conjugation of hydrophilic methoxypoly(ethylene glycol) (PEG) and the targeting ligand of folate (FA) onto their surface. The formed PEG and FA modified Mn3O4 NPs (Mn3O4@SiO2(PEG)–FA) exhibited the good colloidal stability in the simulated biological medium and the targeting ability to HeLa cells overexpressed the FA receptor. The T1-weighted magnetic resonance (MR) imaging and inductively coupled plasma atomic emission spectroscopy (ICP-AES) analysis of Mn3O4@SiO2(PEG)–FA NPs further demonstrated their targeting ability in tumor.
Graphical abstractThe Mn3O4@SiO2(PEG)–FA has been used as a T1-MRI probe for in vivo.Figure optionsDownload full-size imageDownload as PowerPoint slide
