Plasma synthesis of carbon-iron magnetic nanoparticles and immobilization of doxorubicin for targeted drug delivery

被引:6
作者
Ma, Y. [1 ]
Manolache, S.
Denes, F.
Vail, D.
Thamm, D.
Kurzman, I.
机构
[1] Univ Wisconsin, Ctr Plasma Aided Mfg, Madison, WI 53706 USA
[2] Univ Wisconsin, Sch Vet Med, Madison, WI 53706 USA
关键词
doxorubicin; immobilization; magnetic nanoparticles; plasma; targeted drug delivery;
D O I
10.1361/105994906X113705
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A novel dense-medium plasma technology (submerged are discharge) was used to synthesize carbon/iron-based magnetic nanoparticles (CMNP) from benzene or acetonitrile at room temperature and atmospheric pressure. Scanning electron microscopy shows that the nanoparticles are spherical and 40-50 nm in diameter. Results from x-ray photoelectron spectroscopy and other analytical techniques demonstrated that the CMNP consist of iron/iron oxide clusters that are evenly dispersed in a carbon-based host-structure. After synthesis, CMNP samples were activated in three steps: argon plasma treatment, in-situ reactions with ethylene diamine, and substrate activation by glutaric dialdehyde. Free doxorubicin (DOX) molecules were then immobilized onto the activated CMNP surfaces to form CMNP-DOX conjugates. The loading efficiency of doxorubicin was determined. In vitro anti-proliferative activity of CMNP-DOX conjugates was confirmed in tumor-cell cytotoxicity assays. It is therefore suggested that CMNP may be used as a magnetic carrier for targeted drug-delivery applications.
引用
收藏
页码:376 / 382
页数:7
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