Abstract
We report on caged Pt nanoclusters that are able to exert tumor-inside activation for anticancer chemotherapeutics and to minimize systemic toxicity. By shrinking the Pt size to 1 nm, it possesses corrodibility for dissolution in weakly acidic organelles to release toxic Pt ions. The therapeutic effect in exerting tumor-inside activation is confirmed in vivo by post-modifying a pH-cleavable PEG corona and mixing it with a tumor-homing peptide for tumour suppression.
Keywords:
cancer therapy; corrodibility; dendrimers; platinum nanoclusters; tumor-inside activation.
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antineoplastic Agents / administration & dosage
-
Antineoplastic Agents / toxicity
-
Carboplatin / administration & dosage
-
Carboplatin / toxicity
-
Cell Line, Tumor
-
Cell Survival / drug effects
-
Cisplatin / administration & dosage
-
Cisplatin / toxicity
-
Dendrimers / chemistry
-
Drug Carriers / chemistry
-
Humans
-
Magnetic Resonance Imaging
-
Mice
-
Mice, Nude
-
Nanostructures / chemistry*
-
Neoplasms / diagnostic imaging
-
Neoplasms / drug therapy
-
Neoplasms / pathology
-
Platinum / chemistry*
-
Radiography
-
Transplantation, Heterologous
Substances
-
Antineoplastic Agents
-
Dendrimers
-
Drug Carriers
-
Platinum
-
Carboplatin
-
Cisplatin