Triphenylphosphonium-Functionalized Gold Nanorod/Zinc Oxide Core-Shell Nanocomposites for Mitochondrial-Targeted Phototherapy

被引:3
|
作者
Joe, Ara [1 ]
Han, Hyo-Won [1 ]
Lim, Yu-Ra [1 ]
Manivasagan, Panchanathan [1 ]
Jang, Eue-Soon [1 ]
机构
[1] Kumoh Natl Inst Technol, Dept Appl Chem, Gumi 730701, Gyeongbuk, South Korea
关键词
gold nanorods; zinc oxide; triphenylphosphonium; cancer; phototherapy; ENHANCED PHOTODYNAMIC THERAPY; NANOPARTICLES; MECHANISM; ZNO; GROWTH; EFFICIENCY; CLUSTERS; CHITOSAN; LAYER; TUMOR;
D O I
10.3390/pharmaceutics16020284
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Phototherapies, such as photothermal therapy (PTT) and photodynamic therapy (PDT), combined with novel all-in-one light-responsive nanocomposites have recently emerged as new therapeutic modalities for the treatment of cancer. Herein, we developed novel all-in-one triphenylphosphonium-functionalized gold nanorod/zinc oxide core-shell nanocomposites (CTPP-GNR@ZnO) for mitochondrial-targeted PTT/PDT owing to their good biocompatibility, tunable and high optical absorption, photothermal conversion efficiency, highest reactive oxygen species (ROS) generation, and high mitochondrial-targeting capability. Under laser irradiation of 780 nm, the CTPP-GNR@ZnO core-shell nanocomposites effectively produced heat in addition to generating ROS to induce cell death, implying a synergistic effect of mild PTT and PDT in combating cancer. Notably, the in vitro PTT/PDT effect of CTPP-GNR@ZnO core-shell nanocomposites exhibited effective cell ablation (95%) and induced significant intracellular ROS after the 780 nm laser irradiation for 50 min, indicating that CTPP in CTPP-GNR@ZnO core-shell nanocomposites can specifically target the mitochondria of CT-26 cells, as well as generate heat and ROS to completely kill cancer cells. Overall, this light-responsive nanocomposite-based phototherapy provides a new approach for cancer synergistic therapy.
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页数:21
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