Merck
CN
  • Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer.

Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer.

International journal of pharmaceutics (2012-09-11)
L Minati, V Antonini, S Torrengo, M Dalla Serra, M Boustta, X Leclercq, C Migliaresi, M Vert, G Speranza
摘要

Gold nanoparticles functionalized with doxorubicin and stabilized with multilayers of degradable polyelectrolyte were allowed to age in aqueous medium in vitro in order to show the possibility of drug release in cellular environment. The chemico-physical characteristics of the nanoparticles are reported. The observed release of doxorubicin (DOX) was pH-dependent, and it increased in acidic environment. Cell uptake of nanoparticles and drug release were monitored by laser scanning confocal microscopy. Data showed that drug-bearing nanoparticles delivered DOX into the nuclei of A549 cells, leading to pronounced cytotoxic effects to this lung tumor cells. Our results suggest that gold nanoparticles conjugated with doxorubicin could be used as a pH-triggered drug releasing carrier for tumor drug delivery.

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Sigma-Aldrich
聚烯丙基胺盐酸盐, average Mw 50,000
Sigma-Aldrich
聚烯丙基胺盐酸盐, average Mw ~17,500 (GPC vs. PEG std.)
Sigma-Aldrich
聚丙烯胺 溶液, 20 wt. % in H2O
Sigma-Aldrich
聚丙烯胺 溶液, average Mw ~65,000, 10 wt. % in H2O