Dendronized mesoporous silica nanoparticles provide an internal endosomal escape mechanism for successful cytosolic drug release
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文摘

Dendronized mesoporous silica nanoparticles for intracellular drug delivery.

Low cytotoxicity with no impact on the metabolism of endothelial cells.

Specific cancer cell targeting due to receptor-mediated cell uptake.

Redox-driven cleavage of disulfide bridges allows stimuli-responsive cargo release.

Endosomal escape based on the high buffering capacity of PAMAM dendrons.

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