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19F molecular MR imaging for detection of brain tumor angiogenesis: in vivo validation using targeted PFOB nanoparticles
Molecular imaging with magnetic resonance imaging (MRI) targeted contrast agents has emerged as a promising diagnostic approach in cancer research to detect associated biomarkers. In this work, the potential of 19 F MRI was investigated to detect angiogenesis with α ν β 3 -targeted perfluorooctylbro...
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Published in: | Angiogenesis (London) 2013-01, Vol.16 (1), p.171-179 |
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cites | cdi_FETCH-LOGICAL-c372t-6733470c44d0940c5b3c6e9abeb33d6fb6e4e3b93f5c35fa3f34d9124d6ecd0b3 |
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container_title | Angiogenesis (London) |
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creator | Giraudeau, Céline Geffroy, Françoise Mériaux, Sébastien Boumezbeur, Fawzi Robert, Philippe Port, Marc Robic, Caroline Le Bihan, Denis Lethimonnier, Franck Valette, Julien |
description | Molecular imaging with magnetic resonance imaging (MRI) targeted contrast agents has emerged as a promising diagnostic approach in cancer research to detect associated biomarkers. In this work, the potential of
19
F MRI was investigated to detect angiogenesis with α
ν
β
3
-targeted perfluorooctylbromide nanoparticles (PFOB NP) in a U87 glioblastoma mouse model at 7 Tesla. Mice were injected intravenously with targeted or non-targeted NP and
19
F images were immediately acquired for 90 min using a PFOB-dedicated MRI sequence. Mice infused with targeted NP exhibited higher concentrations in tumors than mice of the control group, despite the presence of nonspecific signal originating from the blood. Imaging results were corroborated by histology and fluorescence imaging, suggesting specific binding of targeted NP to α
ν
β
3
integrin. Two other groups of mice were injected 24 h before imaging to allow blood clearance but no significant differences were found between both groups, probably due to a loss of specificity of PFOB NP. This is the first demonstration of the ability of
19
F MRI to detect α
ν
β
3
-integrin endothelial expression in brain tumors in vivo. |
doi_str_mv | 10.1007/s10456-012-9310-0 |
format | article |
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19
F MRI was investigated to detect angiogenesis with α
ν
β
3
-targeted perfluorooctylbromide nanoparticles (PFOB NP) in a U87 glioblastoma mouse model at 7 Tesla. Mice were injected intravenously with targeted or non-targeted NP and
19
F images were immediately acquired for 90 min using a PFOB-dedicated MRI sequence. Mice infused with targeted NP exhibited higher concentrations in tumors than mice of the control group, despite the presence of nonspecific signal originating from the blood. Imaging results were corroborated by histology and fluorescence imaging, suggesting specific binding of targeted NP to α
ν
β
3
integrin. Two other groups of mice were injected 24 h before imaging to allow blood clearance but no significant differences were found between both groups, probably due to a loss of specificity of PFOB NP. This is the first demonstration of the ability of
19
F MRI to detect α
ν
β
3
-integrin endothelial expression in brain tumors in vivo.</description><identifier>ISSN: 0969-6970</identifier><identifier>EISSN: 1573-7209</identifier><identifier>DOI: 10.1007/s10456-012-9310-0</identifier><identifier>PMID: 23053783</identifier><identifier>CODEN: AGIOFT</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain Neoplasms - blood supply ; Brain Neoplasms - diagnosis ; Brain Neoplasms - pathology ; Cancer Research ; Cardiology ; Cell Biology ; Cell Line, Tumor ; Fluorine ; Fluorocarbons - administration & dosage ; Humans ; Injections ; Magnetic Resonance Imaging ; Mice ; Microscopy, Fluorescence ; Molecular Imaging ; Nanoparticles ; Neovascularization, Pathologic ; Oligopeptides ; Oncology ; Ophthalmology ; Original Paper ; Reproducibility of Results ; Xenograft Model Antitumor Assays</subject><ispartof>Angiogenesis (London), 2013-01, Vol.16 (1), p.171-179</ispartof><rights>Springer Science+Business Media Dordrecht 2012</rights><rights>Springer Science+Business Media Dordrecht 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-6733470c44d0940c5b3c6e9abeb33d6fb6e4e3b93f5c35fa3f34d9124d6ecd0b3</citedby><cites>FETCH-LOGICAL-c372t-6733470c44d0940c5b3c6e9abeb33d6fb6e4e3b93f5c35fa3f34d9124d6ecd0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23053783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giraudeau, Céline</creatorcontrib><creatorcontrib>Geffroy, Françoise</creatorcontrib><creatorcontrib>Mériaux, Sébastien</creatorcontrib><creatorcontrib>Boumezbeur, Fawzi</creatorcontrib><creatorcontrib>Robert, Philippe</creatorcontrib><creatorcontrib>Port, Marc</creatorcontrib><creatorcontrib>Robic, Caroline</creatorcontrib><creatorcontrib>Le Bihan, Denis</creatorcontrib><creatorcontrib>Lethimonnier, Franck</creatorcontrib><creatorcontrib>Valette, Julien</creatorcontrib><title>19F molecular MR imaging for detection of brain tumor angiogenesis: in vivo validation using targeted PFOB nanoparticles</title><title>Angiogenesis (London)</title><addtitle>Angiogenesis</addtitle><addtitle>Angiogenesis</addtitle><description>Molecular imaging with magnetic resonance imaging (MRI) targeted contrast agents has emerged as a promising diagnostic approach in cancer research to detect associated biomarkers. In this work, the potential of
19
F MRI was investigated to detect angiogenesis with α
ν
β
3
-targeted perfluorooctylbromide nanoparticles (PFOB NP) in a U87 glioblastoma mouse model at 7 Tesla. Mice were injected intravenously with targeted or non-targeted NP and
19
F images were immediately acquired for 90 min using a PFOB-dedicated MRI sequence. Mice infused with targeted NP exhibited higher concentrations in tumors than mice of the control group, despite the presence of nonspecific signal originating from the blood. Imaging results were corroborated by histology and fluorescence imaging, suggesting specific binding of targeted NP to α
ν
β
3
integrin. Two other groups of mice were injected 24 h before imaging to allow blood clearance but no significant differences were found between both groups, probably due to a loss of specificity of PFOB NP. This is the first demonstration of the ability of
19
F MRI to detect α
ν
β
3
-integrin endothelial expression in brain tumors in vivo.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain Neoplasms - blood supply</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - pathology</subject><subject>Cancer Research</subject><subject>Cardiology</subject><subject>Cell Biology</subject><subject>Cell Line, Tumor</subject><subject>Fluorine</subject><subject>Fluorocarbons - administration & dosage</subject><subject>Humans</subject><subject>Injections</subject><subject>Magnetic Resonance Imaging</subject><subject>Mice</subject><subject>Microscopy, Fluorescence</subject><subject>Molecular Imaging</subject><subject>Nanoparticles</subject><subject>Neovascularization, Pathologic</subject><subject>Oligopeptides</subject><subject>Oncology</subject><subject>Ophthalmology</subject><subject>Original Paper</subject><subject>Reproducibility of Results</subject><subject>Xenograft Model Antitumor Assays</subject><issn>0969-6970</issn><issn>1573-7209</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kV1rFTEQhoNY7LH6A7yRgDferJ18N97Z4tFCpSJ6HbJJdknZTY7J7kH_vTmeKlLwamDmmWdCXoReEHhDANR5JcCF7IDQTjMCHTxCGyIU6xQF_RhtQEvdSa3gFD2t9Q6gNS74E3RKGQimLtgG_SB6i-c8BbdOtuBPX3Cc7RjTiIdcsA9LcEvMCecB98XGhJd1bgObxpjHkEKN9S1u7X3cZ7y3U_T2N7_Wg2OxZWwKjz9vby9xsinvbFmim0J9hk4GO9Xw_L6eoW_b91-vPnY3tx-ur97ddI4punRSMcYVOM49aA5O9MzJoG0fesa8HHoZeGC9ZoNwTAyWDYx7TSj3MjgPPTtDr4_eXcnf11AXM8fqwjTZFPJaDaGKUSIEEQ199QC9y2tJ7XWNklISzalsFDlSruRaSxjMrrQ_Kz8NAXOIxRxjMS0Wc4jFQNt5eW9e-zn4vxt_cmgAPQK1jdIYyj-n_2v9BccimEk</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Giraudeau, Céline</creator><creator>Geffroy, Françoise</creator><creator>Mériaux, Sébastien</creator><creator>Boumezbeur, Fawzi</creator><creator>Robert, Philippe</creator><creator>Port, Marc</creator><creator>Robic, Caroline</creator><creator>Le Bihan, Denis</creator><creator>Lethimonnier, Franck</creator><creator>Valette, Julien</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20130101</creationdate><title>19F molecular MR imaging for detection of brain tumor angiogenesis: in vivo validation using targeted PFOB nanoparticles</title><author>Giraudeau, Céline ; 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In this work, the potential of
19
F MRI was investigated to detect angiogenesis with α
ν
β
3
-targeted perfluorooctylbromide nanoparticles (PFOB NP) in a U87 glioblastoma mouse model at 7 Tesla. Mice were injected intravenously with targeted or non-targeted NP and
19
F images were immediately acquired for 90 min using a PFOB-dedicated MRI sequence. Mice infused with targeted NP exhibited higher concentrations in tumors than mice of the control group, despite the presence of nonspecific signal originating from the blood. Imaging results were corroborated by histology and fluorescence imaging, suggesting specific binding of targeted NP to α
ν
β
3
integrin. Two other groups of mice were injected 24 h before imaging to allow blood clearance but no significant differences were found between both groups, probably due to a loss of specificity of PFOB NP. This is the first demonstration of the ability of
19
F MRI to detect α
ν
β
3
-integrin endothelial expression in brain tumors in vivo.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>23053783</pmid><doi>10.1007/s10456-012-9310-0</doi><tpages>9</tpages></addata></record> |
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source | Springer Nature |
subjects | Animals Biomedical and Life Sciences Biomedicine Brain Neoplasms - blood supply Brain Neoplasms - diagnosis Brain Neoplasms - pathology Cancer Research Cardiology Cell Biology Cell Line, Tumor Fluorine Fluorocarbons - administration & dosage Humans Injections Magnetic Resonance Imaging Mice Microscopy, Fluorescence Molecular Imaging Nanoparticles Neovascularization, Pathologic Oligopeptides Oncology Ophthalmology Original Paper Reproducibility of Results Xenograft Model Antitumor Assays |
title | 19F molecular MR imaging for detection of brain tumor angiogenesis: in vivo validation using targeted PFOB nanoparticles |
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