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Rapidly disassembling nanomicelles with disulfide-linked PEG shells for glutathione-mediated intracellular drug delivery.

Abstract
The synthesis and biological efficacy of novel nanomicelles that rapidly disassemble and release their encapsulated payload intracellularly under tumor-relevant glutathione (GSH) levels are reported. The unique design includes a PEG-sheddable shell and poly(ε-benzyloxycarbonyl-l-lysine) core with a redox-sensitive disulfide linkage.
AuthorsHui-Yun Wen, Hai-Qing Dong, Wen-juan Xie, Yong-Yong Li, Kang Wang, Giovanni M Pauletti, Dong-Lu Shi
JournalChemical communications (Cambridge, England) (Chem Commun (Camb)) Vol. 47 Issue 12 Pg. 3550-2 (Mar 28 2011) ISSN: 1364-548X [Electronic] England
PMID21327187 (Publication Type: Journal Article)
Chemical References
  • Coated Materials, Biocompatible
  • Disulfides
  • Drug Carriers
  • Micelles
  • Polylysine
  • poly(N(epsilon)-benzyloxycarbonyl-L-lysine)
  • Polyethylene Glycols
  • Doxorubicin
  • Glutathione
Topics
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Coated Materials, Biocompatible (chemistry)
  • Disulfides (chemistry)
  • Doxorubicin (metabolism, pharmacology)
  • Drug Carriers (chemistry)
  • Glutathione (chemistry)
  • Humans
  • Intracellular Space (metabolism)
  • Kinetics
  • Micelles
  • Nanostructures (chemistry)
  • Polyethylene Glycols (chemistry)
  • Polylysine (analogs & derivatives, chemistry)

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