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Multifunctional ultrasmall nanoplatforms for vascular-targeted interstitial photodynamic therapy of brain tumors guided by real-time MRI.

Identifieur interne : 000027 ( PubMed/Curation ); précédent : 000026; suivant : 000028

Multifunctional ultrasmall nanoplatforms for vascular-targeted interstitial photodynamic therapy of brain tumors guided by real-time MRI.

Auteurs : Denise Bechet [France] ; Florent Auger [France] ; Pierre Couleaud [France] ; Eric Marty [France] ; Laura Ravasi [France] ; Nicolas Durieux [France] ; Corinne Bonnet ; François Plénat [France] ; Céline Frochot [France] ; Serge Mordon ; Olivier Tillement [France] ; Régis Vanderesse [France] ; François Lux [France] ; Pascal Perriat [France] ; François Guillemin [France] ; Muriel Barberi-Heyob [France]

Source :

RBID : pubmed:25645959

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English descriptors

Abstract

Photodynamic therapy (PDT) for brain tumors appears to be complementary to conventional treatments. A number of studies show the major role of the vascular effect in the tumor eradication by PDT. For interstitial PDT (iPDT) of brain tumors guided by real-time imaging, multifunctional nanoparticles consisting of a surface-localized tumor vasculature targeting neuropilin-1 (NRP-1) peptide and encapsulated photosensitizer and magnetic resonance imaging (MRI) contrast agents, have been designed. Nanoplatforms confer photosensitivity to cells and demonstrate a molecular affinity to NRP-1. Intravenous injection into rats bearing intracranial glioma exhibited a dynamic contrast-enhanced MRI for angiogenic endothelial cells lining the neovessels mainly located in the peripheral tumor. By using MRI completed by NRP-1 protein expression of the tumor and brain adjacent to tumor tissues, we checked the selectivity of the nanoparticles. This study represents the first in vivo proof of concept of closed-head iPDT guided by real-time MRI using targeted ultrasmall nanoplatforms. From the clinical editor: The authors constructed tumor vascular peptide targeting multifunctional silica-based nanoparticles, with encapsulated gadolinium oxide as MRI contrast agent and chlorin as a photosensitizer, as a proof of concept novel treatment for glioblastoma in an animal model.

DOI: 10.1016/j.nano.2014.12.007
PubMed: 25645959

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Corinne Bonnet
<affiliation>
<nlm:affiliation>Laboratoire d'Anatomopathologie, CHU, Vandœuvre-lès-Nancy.</nlm:affiliation>
<wicri:noCountry code="subField">Vandœuvre-lès-Nancy</wicri:noCountry>
</affiliation>
Serge Mordon
<affiliation>
<nlm:affiliation>INSERM U1189, Lille University Hospital, Lille.</nlm:affiliation>
<wicri:noCountry code="subField">Lille</wicri:noCountry>
</affiliation>

Le document en format XML

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<name sortKey="Guillemin, Francois" sort="Guillemin, Francois" uniqKey="Guillemin F" first="François" last="Guillemin">François Guillemin</name>
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<term>Animals</term>
<term>Brain Neoplasms (drug therapy)</term>
<term>Brain Neoplasms (radiography)</term>
<term>Cell Line, Tumor</term>
<term>Female</term>
<term>Glioma (drug therapy)</term>
<term>Glioma (radiography)</term>
<term>Humans</term>
<term>Magnetic Resonance Angiography</term>
<term>Nanoparticles (chemistry)</term>
<term>Nanoparticles (therapeutic use)</term>
<term>Neuropilin-1 (chemistry)</term>
<term>Neuropilin-1 (therapeutic use)</term>
<term>Photochemotherapy (methods)</term>
<term>Photosensitizing Agents (chemistry)</term>
<term>Photosensitizing Agents (pharmacology)</term>
<term>Rats</term>
<term>Rats, Nude</term>
</keywords>
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<term>Angiographie par résonance magnétique</term>
<term>Animaux</term>
<term>Femelle</term>
<term>Gliome ()</term>
<term>Gliome (traitement médicamenteux)</term>
<term>Humains</term>
<term>Lignée cellulaire tumorale</term>
<term>Nanoparticules ()</term>
<term>Nanoparticules (usage thérapeutique)</term>
<term>Neuropiline 1 ()</term>
<term>Neuropiline 1 (usage thérapeutique)</term>
<term>Photosensibilisants ()</term>
<term>Photosensibilisants (pharmacologie)</term>
<term>Photothérapie dynamique ()</term>
<term>Rat nude</term>
<term>Rats</term>
<term>Tumeurs du cerveau ()</term>
<term>Tumeurs du cerveau (traitement médicamenteux)</term>
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<term>Neuropilin-1</term>
<term>Photosensitizing Agents</term>
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<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Nanoparticles</term>
</keywords>
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<term>Brain Neoplasms</term>
<term>Glioma</term>
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</keywords>
<keywords scheme="MESH" qualifier="therapeutic use" xml:lang="en">
<term>Nanoparticles</term>
<term>Neuropilin-1</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Gliome</term>
<term>Tumeurs du cerveau</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Nanoparticules</term>
<term>Neuropiline 1</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cell Line, Tumor</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Angiography</term>
<term>Rats</term>
<term>Rats, Nude</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Angiographie par résonance magnétique</term>
<term>Animaux</term>
<term>Femelle</term>
<term>Gliome</term>
<term>Humains</term>
<term>Lignée cellulaire tumorale</term>
<term>Nanoparticules</term>
<term>Neuropiline 1</term>
<term>Photosensibilisants</term>
<term>Photothérapie dynamique</term>
<term>Rat nude</term>
<term>Rats</term>
<term>Tumeurs du cerveau</term>
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<front>
<div type="abstract" xml:lang="en">Photodynamic therapy (PDT) for brain tumors appears to be complementary to conventional treatments. A number of studies show the major role of the vascular effect in the tumor eradication by PDT. For interstitial PDT (iPDT) of brain tumors guided by real-time imaging, multifunctional nanoparticles consisting of a surface-localized tumor vasculature targeting neuropilin-1 (NRP-1) peptide and encapsulated photosensitizer and magnetic resonance imaging (MRI) contrast agents, have been designed. Nanoplatforms confer photosensitivity to cells and demonstrate a molecular affinity to NRP-1. Intravenous injection into rats bearing intracranial glioma exhibited a dynamic contrast-enhanced MRI for angiogenic endothelial cells lining the neovessels mainly located in the peripheral tumor. By using MRI completed by NRP-1 protein expression of the tumor and brain adjacent to tumor tissues, we checked the selectivity of the nanoparticles. This study represents the first in vivo proof of concept of closed-head iPDT guided by real-time MRI using targeted ultrasmall nanoplatforms. From the clinical editor: The authors constructed tumor vascular peptide targeting multifunctional silica-based nanoparticles, with encapsulated gadolinium oxide as MRI contrast agent and chlorin as a photosensitizer, as a proof of concept novel treatment for glioblastoma in an animal model.</div>
</front>
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<Year>2015</Year>
<Month>04</Month>
<Day>03</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>12</Month>
<Day>21</Day>
</DateCompleted>
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<Volume>11</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2015</Year>
<Month>Apr</Month>
</PubDate>
</JournalIssue>
<Title>Nanomedicine : nanotechnology, biology, and medicine</Title>
<ISOAbbreviation>Nanomedicine</ISOAbbreviation>
</Journal>
<ArticleTitle>Multifunctional ultrasmall nanoplatforms for vascular-targeted interstitial photodynamic therapy of brain tumors guided by real-time MRI.</ArticleTitle>
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<AbstractText>Photodynamic therapy (PDT) for brain tumors appears to be complementary to conventional treatments. A number of studies show the major role of the vascular effect in the tumor eradication by PDT. For interstitial PDT (iPDT) of brain tumors guided by real-time imaging, multifunctional nanoparticles consisting of a surface-localized tumor vasculature targeting neuropilin-1 (NRP-1) peptide and encapsulated photosensitizer and magnetic resonance imaging (MRI) contrast agents, have been designed. Nanoplatforms confer photosensitivity to cells and demonstrate a molecular affinity to NRP-1. Intravenous injection into rats bearing intracranial glioma exhibited a dynamic contrast-enhanced MRI for angiogenic endothelial cells lining the neovessels mainly located in the peripheral tumor. By using MRI completed by NRP-1 protein expression of the tumor and brain adjacent to tumor tissues, we checked the selectivity of the nanoparticles. This study represents the first in vivo proof of concept of closed-head iPDT guided by real-time MRI using targeted ultrasmall nanoplatforms. From the clinical editor: The authors constructed tumor vascular peptide targeting multifunctional silica-based nanoparticles, with encapsulated gadolinium oxide as MRI contrast agent and chlorin as a photosensitizer, as a proof of concept novel treatment for glioblastoma in an animal model.</AbstractText>
<CopyrightInformation>Copyright © 2015 Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Bechet</LastName>
<ForeName>Denise</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>CRAN UMR 7039, CNRS, Vandœuvre-lès-Nancy, France; CRAN UMR 7039, Université de Lorraine, Vandœuvre-lès-Nancy, France.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<ForeName>Pierre</ForeName>
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<Affiliation>LRGP UMR 7274, CNRS, Nancy, France; LRGP UMR 7274, Université de Lorraine, Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Céline</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>LRGP UMR 7274, CNRS, Nancy, France; LRGP UMR 7274, Université de Lorraine, Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mordon</LastName>
<ForeName>Serge</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>INSERM U1189, Lille University Hospital, Lille.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Tillement</LastName>
<ForeName>Olivier</ForeName>
<Initials>O</Initials>
<AffiliationInfo>
<Affiliation>ILM UMR 5306 CNRS, Claude Bernard-University, Lyon, France.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Régis</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<ForeName>Pascal</ForeName>
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<Affiliation>ILM UMR 5306 CNRS, Claude Bernard-University, Lyon, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Guillemin</LastName>
<ForeName>François</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>CRAN UMR 7039, CNRS, Vandœuvre-lès-Nancy, France; CRAN UMR 7039, Université de Lorraine, Vandœuvre-lès-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Barberi-Heyob</LastName>
<ForeName>Muriel</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>CRAN UMR 7039, CNRS, Vandœuvre-lès-Nancy, France; CRAN UMR 7039, Université de Lorraine, Vandœuvre-lès-Nancy, France. Electronic address: muriel.barberi@univ-lorraine.fr.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<Month>01</Month>
<Day>31</Day>
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<MedlineTA>Nanomedicine</MedlineTA>
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<ISSNLinking>1549-9634</ISSNLinking>
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<MeshHeading>
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<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D010778">Photochemotherapy</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000379">methods</QualifierName>
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<MeshHeading>
<DescriptorName MajorTopicYN="Y" UI="D017319">Photosensitizing Agents</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000737">chemistry</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000494">pharmacology</QualifierName>
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<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D051381">Rats</DescriptorName>
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<DescriptorName MajorTopicYN="N" UI="D011923">Rats, Nude</DescriptorName>
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</MeshHeadingList>
<KeywordList Owner="NOTNLM">
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<Keyword MajorTopicYN="N">Multifunctional nanoplatforms</Keyword>
<Keyword MajorTopicYN="N">Real-time MRI</Keyword>
<Keyword MajorTopicYN="N">Targeting</Keyword>
<Keyword MajorTopicYN="N">iPDT</Keyword>
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<Month>5</Month>
<Day>22</Day>
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<Year>2014</Year>
<Month>11</Month>
<Day>21</Day>
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