In Vivo Tracking of the Degradation of Mesoporous Silica through 89Zr Radio-Labeled Core–Shell Nanoparticles

While mesoporous silica nanoparticles (MSNs) are extensively studied as high-potential drug delivery platforms, the successful clinical translation of these nanocarriers strongly depends on their biodistribution, biodegradation, and elimination patterns in vivo. Here, a novel method is reported to f...

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Detalhes bibliográficos
Autores: Bindini, Elisa, Ramirez, Maria de Los Angeles, Rios, Xabier, Cossío, Unai, Simó, Cristina, Gomez Vallejo, Vanessa, Soler Illia, Galo Juan de Avila Arturo, Llop, Jordi, Moya, Sergio E.
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/165534
Acesso em linha:http://hdl.handle.net/11336/165534
Access Level:acceso abierto
Palavra-chave:BIODISTRIBUTION
DEGRADATION
IN VIVO IMAGING
MESOPOROUS SILICA NANOPARTICLES
RADIOLABELING
https://purl.org/becyt/ford/2.10
https://purl.org/becyt/ford/2
Descrição
Resumo:While mesoporous silica nanoparticles (MSNs) are extensively studied as high-potential drug delivery platforms, the successful clinical translation of these nanocarriers strongly depends on their biodistribution, biodegradation, and elimination patterns in vivo. Here, a novel method is reported to follow the in vivo degradation of MSNs by tracking a radioactive label embedded in the silica structure. Core–shell silica nanoparticles (NPs) with a dense core and a mesoporous shell are labeled with low quantities of the positron emitter 89Zr, either in the dense core or in the mesoporous shell. In vivo positron emission tomography imaging and ex vivo organ measurements reveal a remarkable difference in the 89Zr biodistribution between the shell-labeled and the core-labeled NPs. Release of the radiotracer from shell-labeled NPs is used as a probe of the extent of silica dissolution, and a prompt release of the radioisotope is observed, with partial excretion already in the first 2 h post injection, and a slower accumulation in bones over time. On the other hand, when 89Zr is embedded in the nanoparticle core, the biodistribution remains largely unchanged during the first 6 h. These findings indicate that MSNs have fast, hour-scale, degradation kinetics in vivo.