Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells
Mesoporous silica particles (MSP) are major candidates for drug delivery systems due to their versatile, safe, and controllable nature. Understanding their intracellular route and biodegradation process is a challenge, especially when considering their use in neuronal repair. Here, we characterize t...
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doaj-68cb5f4572864bd5a693cf22209746632020-11-25T03:08:25ZengMDPI AGPharmaceutics1999-49232020-05-011248748710.3390/pharmaceutics12060487Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in CellsNerea Iturrioz-Rodríguez0Miguel Ángel Correa-Duarte1Rafael Valiente2Mónica L. Fanarraga3Grupo de Nanomedicina, Instituto Valdecilla-IDIVAL, Herrera Oria s/n, 39011 Santander, SpainBiomedical Research Centre (CINBIO), Universidade de Vigo, 36310 Vigo, SpainGrupo de Nanomedicina, Instituto Valdecilla-IDIVAL, Herrera Oria s/n, 39011 Santander, SpainGrupo de Nanomedicina, Instituto Valdecilla-IDIVAL, Herrera Oria s/n, 39011 Santander, SpainMesoporous silica particles (MSP) are major candidates for drug delivery systems due to their versatile, safe, and controllable nature. Understanding their intracellular route and biodegradation process is a challenge, especially when considering their use in neuronal repair. Here, we characterize the spatiotemporal intracellular destination and degradation pathways of MSP upon endocytosis by HeLa cells and NSC-34 motor neurons using confocal and electron microscopy imaging together with inductively-coupled plasma optical emission spectroscopy analysis. We demonstrate how MSP are captured by receptor-mediated endocytosis and are temporarily stored in endo-lysosomes before being finally exocytosed. We also illustrate how particles are often re-endocytosed after undergoing surface erosion extracellularly. On the other hand, silica particles engineered to target the cytosol with a carbon nanotube coating, are safely dissolved intracellularly in a time scale of hours. These studies provide fundamental clues for programming the sub-cellular fate of MSP and reveal critical aspects to improve delivery strategies and to favor MSP safe elimination. We also demonstrate how the cytosol is significantly more corrosive than lysosomes for MSP and show how their biodegradation is fully biocompatible, thus, validating their use as nanocarriers for nervous system cells, including motor neurons.https://www.mdpi.com/1999-4923/12/6/487silica nanocarriercytoplasmic escapebiodegradationengineering nanoparticlesHeLamotor neurons |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nerea Iturrioz-Rodríguez Miguel Ángel Correa-Duarte Rafael Valiente Mónica L. Fanarraga |
spellingShingle |
Nerea Iturrioz-Rodríguez Miguel Ángel Correa-Duarte Rafael Valiente Mónica L. Fanarraga Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells Pharmaceutics silica nanocarrier cytoplasmic escape biodegradation engineering nanoparticles HeLa motor neurons |
author_facet |
Nerea Iturrioz-Rodríguez Miguel Ángel Correa-Duarte Rafael Valiente Mónica L. Fanarraga |
author_sort |
Nerea Iturrioz-Rodríguez |
title |
Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells |
title_short |
Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells |
title_full |
Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells |
title_fullStr |
Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells |
title_full_unstemmed |
Engineering Sub-Cellular Targeting Strategies to Enhance Safe Cytosolic Silica Particle Dissolution in Cells |
title_sort |
engineering sub-cellular targeting strategies to enhance safe cytosolic silica particle dissolution in cells |
publisher |
MDPI AG |
series |
Pharmaceutics |
issn |
1999-4923 |
publishDate |
2020-05-01 |
description |
Mesoporous silica particles (MSP) are major candidates for drug delivery systems due to their versatile, safe, and controllable nature. Understanding their intracellular route and biodegradation process is a challenge, especially when considering their use in neuronal repair. Here, we characterize the spatiotemporal intracellular destination and degradation pathways of MSP upon endocytosis by HeLa cells and NSC-34 motor neurons using confocal and electron microscopy imaging together with inductively-coupled plasma optical emission spectroscopy analysis. We demonstrate how MSP are captured by receptor-mediated endocytosis and are temporarily stored in endo-lysosomes before being finally exocytosed. We also illustrate how particles are often re-endocytosed after undergoing surface erosion extracellularly. On the other hand, silica particles engineered to target the cytosol with a carbon nanotube coating, are safely dissolved intracellularly in a time scale of hours. These studies provide fundamental clues for programming the sub-cellular fate of MSP and reveal critical aspects to improve delivery strategies and to favor MSP safe elimination. We also demonstrate how the cytosol is significantly more corrosive than lysosomes for MSP and show how their biodegradation is fully biocompatible, thus, validating their use as nanocarriers for nervous system cells, including motor neurons. |
topic |
silica nanocarrier cytoplasmic escape biodegradation engineering nanoparticles HeLa motor neurons |
url |
https://www.mdpi.com/1999-4923/12/6/487 |
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