Abstract
1914
Objectives To study on the immunocompetence, biological distribution in vivo, liver targeting and tumor inhibition of 188Re-immunomagnetite nanoparticle(188Re-HMN), thus to provide a biological-magnetic double targeting radiotherapy for primary hepatocellular carcinoma.
Methods By setting up 188ReO4- group, 188Re-Hepama group and 188Re-magnetite nanoparticle group, the distributions of 188Re-HMN in liver, spleen, kidney, lung, stomach, blood, brain, femoral bone and muscle were investigated 4h, 24h after the particles were injected into tail vein of Kunming mouse. The particles were also injected into New Zealand rabbit, the hepatic magnetic targeting in vivo was studied when magnetic field was attached or not onto hepatic region. MMT method was adopted to study the inhibiting effects of 4 188Re markers on hepatoma cell strain SMMC-7721.
Results After the particles were intravenously injected into mice for 4h and 24 h, there was significantly difference in 188Re-HMN group compared to 188ReO4- group, 188R-Hepama group and 188Re-magnetite nanoparticle group (ρ<0.01), and 188Re-HMN group had the most uptake. After magnetic field applied on left lateral lobe , in 188Re-HMN group, and radio-activity of magnetic field was obviously increased compared to that of non-magnetic field (ρ=0.000), and the radio-activity ratio of them was 1.87. The inhibition rates against hepatocellular carcinoma SMMC-7721 cells of 188Re-HMN group were significantly higher than those groups (P<0.05).
Conclusions 188Re-immuno-magnetite nanoparticle provides a helpful prospect for biological magnetic targeting therapy against primary hepatocellular carcinoma.

- © 2009 by Society of Nuclear Medicine