PEGylated PAMAM dendrimer-doxorubicin conjugate-hybridized gold nanorod for combined photothermal-chemotherapy

被引:169
|
作者
Li, Xiaojie [1 ]
Takashima, Munenobu [1 ]
Yuba, Eiji [1 ]
Harada, Atsushi [1 ]
Kono, Kenji [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Naka Ku, Sakai, Osaka 5998531, Japan
关键词
Dendrimer; Gold nanorods; Photothermal therapy; Chemotherapy; Doxorubicin; CANCER THERMO-CHEMOTHERAPY; TRIGGERED DRUG-RELEASE; THERAPY; NANOPARTICLES; DELIVERY; AGENTS; LIGHT; HYPERTHERMIA; NANOSHELLS; NANOCAGES;
D O I
10.1016/j.biomaterials.2014.04.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We prepared pH-sensitive drug dendrimer conjugate-hybridized gold nanorod as a promising platform for combined cancer photothermal-chemotherapy under in vitro and in vivo conditions. Poly(ethylene glycol)-attached PAMAM G4 dendrimers (PEG PAMAM) were first covalently linked on the surface of mercaptohexadecanoic acid-functionalized gold nanorod (MHA-AuNR), with subsequent conjugation of anti-cancer drug doxorubicin (DOX) to dendrimer layer using an acid-labile-hydrazone linkage to afford PEG-DOX-PAMAM-AuNR particles. The particles with a high PEG PAMAM dendrimer coverage density (0.28 per nm(2) AuNR) showed uniform sizes and excellent colloidal stability. In vitro drug release studies demonstrated that DOX released from PEG DOX PAMAM AuNR was negligible under normal physiological pH, but it was enhanced significantly at a weak acidic pH value. The efficient intracellular acid-triggered DOX release inside of lysosomes was confirmed using confocal laser scanning microscopy analysis. Furthermore, the combined photothermal-chemo treatment of cancer cells using PEG DOX PAMAM AuNR for synergistic hyperthermia ablation and chemotherapy was demonstrated both in vitro and in vivo to exhibit higher therapeutic efficacy than either single treatment alone, underscoring the great potential of PEG DOX PAMAM AuNR particles for cancer therapy. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6576 / 6584
页数:9
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