Quantitative Evaluation of the Reticuloendothelial System Function with Dynamic MRI
Author(s) -
Ting Liu,
Hoon Choi,
Rong Zhou,
IWei Chen
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0103576
Subject(s) - mononuclear phagocyte system , magnetic resonance imaging , dynamic contrast enhanced mri , liposome , compartment (ship) , chemistry , nuclear medicine , kupffer cell , pharmacokinetics , biomedical engineering , medicine , pathology , biochemistry , radiology , oceanography , geology
Purpose To evaluate the reticuloendothelial system (RES) function by real-time imaging blood clearance as well as hepatic uptake of superparamagnetic iron oxide nanoparticle (SPIO) using dynamic magnetic resonance imaging (MRI) with two-compartment pharmacokinetic modeling. Materials and Methods Kinetics of blood clearance and hepatic accumulation were recorded in young adult male 01b74 athymic nude mice by dynamic T2* weighted MRI after the injection of different doses of SPIO nanoparticles (0.5, 3 or 10 mg Fe/kg). Association parameter, K in , dissociation parameter, K out , and elimination constant, K e , derived from dynamic data with two-compartment model, were used to describe active binding to Kupffer cells and extrahepatic clearance. The clodrosome and liposome were utilized to deplete macrophages and block the RES function to evaluate the capability of the kinetic parameters for investigation of macrophage function and density. Results The two-compartment model provided a good description for all data and showed a low sum squared residual for all mice (0.27±0.03). A lower K in , a lower K out and a lower K e were found after clodrosome treatment, whereas a lower K in , a higher K out and a lower K e were observed after liposome treatment in comparison to saline treatment (P<0.005). Conclusion Dynamic SPIO-enhanced MR imaging with two-compartment modeling can provide information on RES function on both a cell number and receptor function level.
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