The optimization of cancer photodynamic therapy by utilization of a pi-extended porphyrin-type photosensitizer in combination with MITO-Porter

被引:40
作者
Satrialdi [1 ,2 ]
Munechika, Reina [1 ]
Biju, Vasudevanpillai [3 ,4 ]
Takano, Yuta [3 ,4 ]
Harashima, Hideyoshi [1 ]
Yamada, Yuma [1 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12,Nishi 6, Sapporo, Hokkaido 0600812, Japan
[2] Inst Teknol Bandung, Sch Pharm, Ganesha 10, Bandung 40132, Indonesia
[3] Hokkaido Univ, Res Inst Elect Sci, Kita Ku, Kita 20 Nishi 10, Sapporo, Hokkaido 0010020, Japan
[4] Hokkaido Univ, Grad Sch Environm Sci, Kita Ku, Kita 10 Nishi 5, Sapporo, Hokkaido 0600810, Japan
关键词
MITOCHONDRIAL DELIVERY; CELLS; MACROMOLECULE; ACTIVATION; MECHANISMS; APOPTOSIS;
D O I
10.1039/c9cc08563g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The uncontrolled production of reactive oxygen species during photodynamic therapy (PDT) induces oxidative stress. The full potential of PDT is accomplished by delivery of a pi-extended porphyrin-type photosensitizer into mitochondria of tumor cells using a MITO-Porter, a mitochondrial targeting nanodevice. This strategy can be implemented for innovative cancer therapy.
引用
收藏
页码:1145 / 1148
页数:4
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