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Cited by 359

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pH-Sensitive ZnO Quantum Dots–Doxorubicin Nanoparticles for Lung Cancer Targeted Drug Delivery

Cai, Xiaoli, Luo, Yanan, Zhang, Weiying, Du, Dan, Lin, Yuehe·2016·ACS Applied Materials & Interfaces

Abstract

In this paper, we reported a ZnO quantum dots-based pH-responsive drug delivery platform for intracellular controlled release of drugs. Acid-decomposable, luminescent aminated ZnO quantum dots (QDs) were synthesized as nanocarriers with ultrasmall size (∼3 nm). The dicarboxyl-terminated poly(ethylene glycol) (PEG) had been introduced to NH2-ZnO QDs, which rendered it stable under physiological fluid. Moreover, a targeting ligand, hyaluronic acid (HA), was conjugated to ZnO QDs for specifically binding to the overexpressed glycoprotein CD44 by cancer cells. Doxorubicin (DOX) molecules were successfully loaded to PEG functionalized ZnO QDs via formation of metal-DOX complex and covalent interactions. The pH-sensitive ZnO QDs dissolved to Zn(2+) in acidic endosome/lysosome after uptake by cancer cells, which triggered dissociation of the metal-drug complex and a controlled DOX release. As result, a synergistic therapy was achieved due to incorporation of the antitumor effect of Zn(2+) and DOX.

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Authors
Cai, X., Luo, Y., Zhang, W., Du, D., & Lin, Y.
Venue
ACS Applied Materials & Interfaces
Published
2016-08-19
Volume
8
Issue
34
Pages
22442-22450
ISSN
  • 1944-8244 (ISSN-L)
  • 1944-8252
OpenAlex
W2490849378
Cited by
359
References
0
FWCI
12.03
Type
journal article
Language
en
Open access
closed

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