Pharmacokinetics and MR imaging of SPIO-shRNA dual functional molecular probe in vivo.
- Author:
Xiao-lin DENG
;
Xiao-dong GE
;
Xiao-feng WU
;
Mei-ling LI
;
Rui-kun LIAO
;
Dan-ni ZENG
;
Ming WEN
- Publication Type:Journal Article
- MeSH:
Animals;
Half-Life;
Magnetic Resonance Imaging;
Magnetite Nanoparticles;
Mice;
Molecular Probes;
pharmacokinetics;
RNA, Small Interfering;
chemistry;
Rabbits
- From:
Acta Pharmaceutica Sinica
2015;50(10):1285-1289
- CountryChina
- Language:Chinese
-
Abstract:
In this study, we investigated the pharmacokinetics parameters of SPIO-shRNA dual functional molecular probe and observed the main organ distribution by MRI in vivo. Eighteen New Zealand white rabbits were randomly divided into three groups and injected intravenously with different doses of SPIO-shRNA molecular probe, respectively. The blood samples were collected to analyze the pharmacokinetic parameters by measuring the iron content at 30 minutes before and after the injection. Twenty-four Kun Ming (KM) mice were randomly divided into 4 groups: the control group was injected intravenously with physiological saline 200 µL per mouse via the tail vein, the other 3 groups were injected intravenously with different doses of SPIO-shRNA molecular probe. MRI observation was performed in 24 hours, and the liver, spleen, kidney, brain and muscle were collected for iron quantification with Prussian blue staining to determine distribution of the SPIO-shRNA molecular probe in the main organ in vivo. Our results suggest that the molecular probe blood half-life is more than 3 hours. The data of MRI suggest the probe was distributed in liver and spleen, and the MRI signal was reduced with the increase in probe's doses (P < 0.05). The results of Prussian blue staining confirmed the results of MRI. Most of the probe could escape the phagocytosis of mononuclear phagocyte system. Our data provide the pharmacokinetic and distribution of SPIO-shRNA molecular probe in organs. Meanwhile, it suggests the choice of the time and dose of probe for MR imaging of tumor in vivo.
