Spherically-clustered porous Au-Ag alloy nanoparticle prepared by partial inhibition of galvanic replacement and its application for efficient multimodal therapy.

Spherically-clustered porous Au-Ag alloy nanoparticle prepared by partial inhibition of galvanic replacement and its application for efficient multimodal therapy.

ACS nano (2015-01-07)

Hongje Jang, Dal-Hee Min

RÉSUMÉ

The polyvinylpyrrolidone (PVP)-coated spherically clustered porous gold-silver alloy nanoparticle (PVP-SPAN) was prepared by low temperature mediated, partially inhibited galvanic replacement reaction followed by silver etching process. The prepared porous nanostructures exhibited excellent photothermal conversion efficiency under irradiation of near-infrared light (NIR) and allowed a high payload of both doxorubicin (Dox) and thiolated dye-labeled oligonucleotide, DNAzyme (FDz). Especially, PVP-SPAN provided 10 times higher loading capacity for oligonucleotide than conventional hollow nanoshells due to increased pore diameter and surface-to-volume ratio. We demonstrated highly efficient chemo-thermo-gene multitherapy based on codelivery of Dox and FDz with NIR-mediated photothermal therapeutic effect using a model system of hepatitis C virus infected human liver cells (Huh7 human hepatocarcinoma cell line containing hepatitis C virus NS3 gene replicon) compared to conventional hollow nanoshells.

MATÉRIAUX

Référence du produit

Marque

Description du produit

216763

Sigma-Aldrich

Peroxyde d'hydrogène solution, contains inhibitor, 30 wt. % in H₂O, ACS reagent

H1009

Sigma-Aldrich

Peroxyde d'hydrogène solution, 30 % (w/w) in H₂O, contains stabilizer

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Bleu de thiazol (thiazolyl blue tetrazolium bromide), 98%

516813

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Peroxyde d'hydrogène solution, 50 wt. % in H₂O, stabilized

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Bleu de thiazol (thiazolyl blue tetrazolium bromide), powder, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥97.5% (HPLC)

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Doxorubicine hydrochloride, 98.0-102.0% (HPLC)

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Peroxyde d'hydrogène solution, 30% (w/w), puriss. p.a., reag. ISO, reag. Ph. Eur.

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