Accumulation of inorganic nanostructures in the excretory system organs increases their likelihood of toxicity and interference with common medical diagnoses. Thus, one of the major concerns regarding their clinical translation is related to their persistence in organisms. Here the authors demonstrate that nano-architectures composed by hollow silica nanocapsules embedding arrays of ultrasmall gold nanoparticles undergo biodegradation in cellular environment affording small, potentially clearable building blocks. Furthermore, the authors present their exploitation in glutathione-triggered release of covalently loaded cisplatin prodrug. This endogenously triggered release leads to high cytotoxicity to human pancreatic carcinoma cells, setting the way for promising applications to synergistic dual chemo/radio-therapy and radio-imaging.

Biodegradable passion fruit-like nano-architectures as carriers for cisplatin prodrug

Cassano, Domenico;Santi, Melissa;Luin, Stefano;Signore, Giovanni;Voliani, Valerio
2016

Abstract

Accumulation of inorganic nanostructures in the excretory system organs increases their likelihood of toxicity and interference with common medical diagnoses. Thus, one of the major concerns regarding their clinical translation is related to their persistence in organisms. Here the authors demonstrate that nano-architectures composed by hollow silica nanocapsules embedding arrays of ultrasmall gold nanoparticles undergo biodegradation in cellular environment affording small, potentially clearable building blocks. Furthermore, the authors present their exploitation in glutathione-triggered release of covalently loaded cisplatin prodrug. This endogenously triggered release leads to high cytotoxicity to human pancreatic carcinoma cells, setting the way for promising applications to synergistic dual chemo/radio-therapy and radio-imaging.
2016
Settore FIS/03 - Fisica della Materia
Settore CHIM/03 - Chimica Generale e Inorganica
Settore BIO/09 - Fisiologia
biodegradation; cisplatin; gold nanoparticle; hollow silica; human pancreatic carcinoma;
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11384/64307
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