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In vivo hepatocyte MR imaging using lactose functionalized magnetoliposomes
Authors:Ashwini Ketkar-Atre  Tom Struys  Tom Dresselaers  Michael Hodenius  Inge Mannaerts  Yicheng Ni  Ivo Lambrichts  Leo A. Van Grunsven  Marcel De Cuyper  Uwe Himmelreich
Affiliation:1. Biomedical MRI/MoSAIC, Department of Imaging and Pathology, Biomedical Sciences Group, Katholieke Universiteit Leuven, Herestraat 49, B3000 Leuven, Belgium;2. Lab of Histology, Biomedical Research Institute, Hasselt University, Campus Diepenbeek, Agoralaan, B3590 Diepenbeek, Belgium;3. Laboratory of BioNanoColloids, Interdisciplinary Research Centre, Katholieke Universiteit Leuven, Etienne Sabbelaan 53, B8500 Kortrijk, Belgium;4. Department of Cell Biology, Liver Cell Biology Lab, Vrije Universiteit Brussel, Laarbeeklaan 103, B1090 Brussel-Jette, Belgium;5. Theragnostic Laboratory, Department of Imaging and Pathology, Biomedical Sciences Group, Katholieke Universiteit Leuven, Herestraat 49, B3000 Leuven, Belgium
Abstract:The aim of this study was to assess a novel lactose functionalized magnetoliposomes (MLs) as an MR contrast agent to target hepatocytes as well as to evaluate the targeting ability of MLs for in vivo applications. In the present work, 17 nm sized iron oxide cores functionalized with anionic MLs bearing lactose moieties were used for targeting the asialoglycoprotein receptor (ASGP-r), which is highly expressed in hepatocytes. Non-functionalized anionic MLs were tested as negative controls. The size distribution of lactose and anionic MLs was determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). After intravenous administration of both MLs, contrast enhancement in the liver was observed by magnetic resonance imaging (MRI). Label retention was monitored non-invasively by MRI and validated with Prussian blue staining and TEM for up to eight days post MLs administration. Although the MRI signal intensity did not show significant differences between functionalized and non-functionalized particles, iron-specific Prussian blue staining and TEM analysis confirmed the uptake of lactose MLs mainly in hepatocytes. In contrast, non-functionalized anionic MLs were mainly taken up by Kupffer and sinusoidal cells. Target specificity was further confirmed by high-resolution MR imaging of phantoms containing isolated hepatocytes, Kupffer cell (KCs) and hepatic stellate cells (HSCs) fractions. Hypointense signal was observed for hepatocytes isolated from animals which received lactose MLs but not from animals which received anionic MLs. These data demonstrate that galactose-functionalized MLs can be used as a hepatocyte targeting MR contrast agent to potentially aid in the diagnosis of hepatic diseases if the non-specific uptake by KCs is taken into account.
Keywords:Asialoglycoprotein receptor (ASGPr-1)   Hepatocyte   Liver   MRI   Lactose   Magnetoliposomes
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