Galactosylated manganese ferrite nanoparticles for targeted MR imaging of asialoglycoprotein receptor

Cancer cells can express specific biomarkers, such as cell membrane proteins and signaling factors. Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The a...

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Veröffentlicht in:Nanotechnology 2013-11, Vol.24 (47), p.475103-475103
Hauptverfasser: Yang, Seung-Hyun, Heo, Dan, Lee, Eugene, Kim, Eunjung, Lim, Eun-Kyung, Lee, Young Han, Haam, Seungjoo, Suh, Jin-Suck, Huh, Yong-Min, Yang, Jaemoon, Park, Sahng Wook
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container_end_page 475103
container_issue 47
container_start_page 475103
container_title Nanotechnology
container_volume 24
creator Yang, Seung-Hyun
Heo, Dan
Lee, Eugene
Kim, Eunjung
Lim, Eun-Kyung
Lee, Young Han
Haam, Seungjoo
Suh, Jin-Suck
Huh, Yong-Min
Yang, Jaemoon
Park, Sahng Wook
description Cancer cells can express specific biomarkers, such as cell membrane proteins and signaling factors. Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The asialoglycoprotein receptor (ASGPr) was selected as a biomarker for hepatoma cells and the ASGPr-targetable imaging agent bearing a galactosyl group was prepared using manganese ferrite nanoparticles (MFNP) and galactosylgluconic acid. The utility of the ASGPr-targetable imaging agent, galactosylated MFNP (G-MFNP) was assessed by several methods in ASGPr-expressing HepG2 cells as target cells and ASGPr-deficient MCF7 cells. Physical and chemical properties of G-MFNP were examined using Fourier-transform infrared spectroscopy, dynamic light scattering, zeta potential analysis, and transmission electron microscopy. No significant cytotoxicity was observed in either cell line. Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. We suggest that these results will be useful in strategies for cancer diagnoses based on magnetic resonance imaging.
doi_str_mv 10.1088/0957-4484/24/47/475103
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Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The asialoglycoprotein receptor (ASGPr) was selected as a biomarker for hepatoma cells and the ASGPr-targetable imaging agent bearing a galactosyl group was prepared using manganese ferrite nanoparticles (MFNP) and galactosylgluconic acid. The utility of the ASGPr-targetable imaging agent, galactosylated MFNP (G-MFNP) was assessed by several methods in ASGPr-expressing HepG2 cells as target cells and ASGPr-deficient MCF7 cells. Physical and chemical properties of G-MFNP were examined using Fourier-transform infrared spectroscopy, dynamic light scattering, zeta potential analysis, and transmission electron microscopy. No significant cytotoxicity was observed in either cell line. Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. 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Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. 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Heo, Dan ; Lee, Eugene ; Kim, Eunjung ; Lim, Eun-Kyung ; Lee, Young Han ; Haam, Seungjoo ; Suh, Jin-Suck ; Huh, Yong-Min ; Yang, Jaemoon ; Park, Sahng Wook</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-99f9619277d2f9a5d846fd6e645fd70c079b61657c2bf8294dc1fca082bc3b683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Absorbance</topic><topic>Asialoglycoprotein Receptor - metabolism</topic><topic>Colloids - chemistry</topic><topic>Cross-disciplinary physics: materials science; rheology</topic><topic>Electron microscopy</topic><topic>Exact sciences and technology</topic><topic>Ferric Compounds - metabolism</topic><topic>Flow cytometry</topic><topic>Fluorescence</topic><topic>Galactose - metabolism</topic><topic>Glycosylation</topic><topic>Hep G2 Cells</topic><topic>Humans</topic><topic>Imaging</topic><topic>Inductively coupled plasma</topic><topic>Magnetic Resonance Imaging</topic><topic>Manganese Compounds - metabolism</topic><topic>Materials science</topic><topic>MCF-7 Cells</topic><topic>Microscopy</topic><topic>Nanocrystalline materials</topic><topic>Nanoparticles - chemistry</topic><topic>Nanoparticles - ultrastructure</topic><topic>Nanoscale materials and structures: fabrication and characterization</topic><topic>Particle Size</topic><topic>Physics</topic><topic>Spectrophotometry, Atomic</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Staining</topic><topic>Static Electricity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Seung-Hyun</creatorcontrib><creatorcontrib>Heo, Dan</creatorcontrib><creatorcontrib>Lee, Eugene</creatorcontrib><creatorcontrib>Kim, Eunjung</creatorcontrib><creatorcontrib>Lim, Eun-Kyung</creatorcontrib><creatorcontrib>Lee, Young Han</creatorcontrib><creatorcontrib>Haam, Seungjoo</creatorcontrib><creatorcontrib>Suh, Jin-Suck</creatorcontrib><creatorcontrib>Huh, Yong-Min</creatorcontrib><creatorcontrib>Yang, Jaemoon</creatorcontrib><creatorcontrib>Park, Sahng Wook</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; 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Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The asialoglycoprotein receptor (ASGPr) was selected as a biomarker for hepatoma cells and the ASGPr-targetable imaging agent bearing a galactosyl group was prepared using manganese ferrite nanoparticles (MFNP) and galactosylgluconic acid. The utility of the ASGPr-targetable imaging agent, galactosylated MFNP (G-MFNP) was assessed by several methods in ASGPr-expressing HepG2 cells as target cells and ASGPr-deficient MCF7 cells. Physical and chemical properties of G-MFNP were examined using Fourier-transform infrared spectroscopy, dynamic light scattering, zeta potential analysis, and transmission electron microscopy. No significant cytotoxicity was observed in either cell line. Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. We suggest that these results will be useful in strategies for cancer diagnoses based on magnetic resonance imaging.</abstract><cop>Bristol</cop><pub>IOP Publishing</pub><pmid>24192299</pmid><doi>10.1088/0957-4484/24/47/475103</doi><tpages>9</tpages></addata></record>
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source MEDLINE; IOP Publishing Journals; Institute of Physics (IOP) Journals - HEAL-Link
subjects Absorbance
Asialoglycoprotein Receptor - metabolism
Colloids - chemistry
Cross-disciplinary physics: materials science
rheology
Electron microscopy
Exact sciences and technology
Ferric Compounds - metabolism
Flow cytometry
Fluorescence
Galactose - metabolism
Glycosylation
Hep G2 Cells
Humans
Imaging
Inductively coupled plasma
Magnetic Resonance Imaging
Manganese Compounds - metabolism
Materials science
MCF-7 Cells
Microscopy
Nanocrystalline materials
Nanoparticles - chemistry
Nanoparticles - ultrastructure
Nanoscale materials and structures: fabrication and characterization
Particle Size
Physics
Spectrophotometry, Atomic
Spectroscopy, Fourier Transform Infrared
Staining
Static Electricity
title Galactosylated manganese ferrite nanoparticles for targeted MR imaging of asialoglycoprotein receptor
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