In situ real-time investigation of cancer cell photothermolysis mediated by excited gold nanorod surface plasmons

被引:90
作者
Chen, Cheng-Lung [1 ,2 ]
Kuo, Ling-Ru [3 ]
Chang, Ching-Lin [3 ]
Hwu, Yeu-Kuang [1 ]
Huang, Cheng-Kuang [1 ]
Lee, Shin-Yu [1 ]
Chen, Kowa [1 ]
Lin, Su-Jien [2 ]
Huang, Jing-Duan [4 ]
Chen, Yang-Yuan [1 ]
机构
[1] Acad Sinica, Inst Phys, Taipei, Taiwan
[2] Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu, Taiwan
[3] Tamkang Univ, Dept Phys, Tamsui, Taiwan
[4] Natl Taiwan Ocean Univ, Inst Marine Biol, Taipei, Taiwan
关键词
Gold; Plasma; Membrane; Laser; Fluorescence; NANOPARTICLES; GROWTH; DEATH; CYTOTOXICITY; LYSOSOMES; THERAPY; ASSAY;
D O I
10.1016/j.biomaterials.2010.01.140
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The photothermolysis of living EMT-6 breast tumor cells triggered by gold nanorods (AuNRs) with two-photon irradiation was conducted in situ and under real-time observation. The morphology and plasma membrane permeability of the cells were key indicators to the phenomena. AuNRs with an aspect ratio of 3.92, and a longitudinal absorption peak at 300 nm were synthesized with a seed-mediated method. The nanorods surfaces were further modified with polystyrenesulfonate (PSS) for biocompatibility. The prepared nanorods displayed excellent two-photon photoluminescence imaging. In situ real-time results revealed cavities internal to the cells were created from thermal explosions triggered by AuNRs localized photothermal effect. The cavitation dynamic is energy dependent and responsible for the perforation or sudden rupture of the plasma membrane. The energy threshold for cell therapy depended significantly on the number of nanorods taken up per cell. For an ingested AuNR cluster quantity N similar to 10-30 per cell, it is found that energy fluences E larger-than 93 mJ/cm(2) led to effective cell destruction in the crumbled form within a very short period. As for a lower energy level E = 18 mJ/cm(2) with N similar to 60-100, a non-instant, but progressive cell deterioration, is observed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4104 / 4112
页数:9
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