Novel methodology for labelling mesoporous silica nanoparticles using the ^sup 18^F isotope and their in vivo biodistribution by positron emission tomography

Nanoparticles have been proposed for several biomedical applications due to their potential as drug carriers, diagnostic and therapeutic agents. However, only a few of them have been approved for their use in humans. In order to gauge the potential applicability of a specific type of nanoparticle, i...

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Veröffentlicht in:Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2015-03, Vol.17 (3), p.1
Hauptverfasser: Rojas, Santiago, Gispert, Juan Domingo, Menchón, Cristina, Baldoví, Herme G, Buaki-sogo, Mireia, Rocha, Milagros, Abad, Sergio, Victor, Victor Manuel, García, Hermenegildo, Herance, José Raúl
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container_title Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology
container_volume 17
creator Rojas, Santiago
Gispert, Juan Domingo
Menchón, Cristina
Baldoví, Herme G
Buaki-sogo, Mireia
Rocha, Milagros
Abad, Sergio
Victor, Victor Manuel
García, Hermenegildo
Herance, José Raúl
description Nanoparticles have been proposed for several biomedical applications due to their potential as drug carriers, diagnostic and therapeutic agents. However, only a few of them have been approved for their use in humans. In order to gauge the potential applicability of a specific type of nanoparticle, in vivo biodistribution studies to characterize their pharmacokinetic properties are essential. In this regard, mesoporous silica nanoparticles (30-130 nm) have been functionalized with amino groups in order to react with N-succinimidyl 4-[^sup 18^F]fluorobenzoate and thus anchor the ^sup 18^F positron emission isotope by using a novel and easy labelling strategy. In vivo biodistribution was characterized in mice after intravenous administration of radiolabelled nanoparticles by positron emission tomography. Our results indicated that radiolabelled mesoporous silica nanoparticles were excreted into bile and urine and accumulated mainly in the organs of the reticuloendothelial system and lungs.
doi_str_mv 10.1007/s11051-015-2938-0
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Intravenous administration
Nanoparticles
Pharmacokinetics
Silica
title Novel methodology for labelling mesoporous silica nanoparticles using the ^sup 18^F isotope and their in vivo biodistribution by positron emission tomography
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