Abstract
Rationally designed PIC nanoparticles as next-generation delivery system: we have developed a core-shell-corona PIC nanoparticle (⊕) NP/Pt@PPC-DA as a next-generation delivery system. (⊕) NP/Pt@PPC-DA exhibits prolonged circulation and enhanced drug accumulation in tumors. Subsequently, tumor pH leads to the release of (⊕) NP/Pt, which facilitates cellular uptake followed by rapid intracellular cisplatin release. Using this delivery strategy cisplatin-resistant tumor growth in a murine xenograft model has been successfully suppressed.
Keywords:
PIC nanoparticles; cisplatin resistance; drug delivery; tumor pH-responsive.
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adenocarcinoma / drug therapy
-
Adenocarcinoma / metabolism
-
Adenocarcinoma / pathology
-
Animals
-
Antineoplastic Agents / administration & dosage*
-
Antineoplastic Agents / blood
-
Antineoplastic Agents / chemistry
-
Cell Line, Tumor
-
Cisplatin / administration & dosage*
-
Cisplatin / blood
-
Cisplatin / chemistry
-
Drug Resistance, Neoplasm*
-
Humans
-
Hydrogen-Ion Concentration
-
Lung Neoplasms / drug therapy
-
Lung Neoplasms / metabolism
-
Lung Neoplasms / pathology
-
Mice
-
Mice, Nude
-
Nanoconjugates* / administration & dosage
-
Nanoconjugates* / chemistry
-
Platinum / chemistry
-
Platinum / metabolism
-
Prodrugs / administration & dosage
-
Prodrugs / chemistry
-
Prodrugs / metabolism
-
Xenograft Model Antitumor Assays
Substances
-
Antineoplastic Agents
-
Nanoconjugates
-
Prodrugs
-
Platinum
-
Cisplatin