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利用激发态金纳米棒表面等离激元介导的癌细胞光热溶解的原位实时研究。

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

机构信息

Institute of Physics, Academia Sinica, Taipei, Taiwan, ROC.

出版信息

Biomaterials. 2010 May;31(14):4104-12. doi: 10.1016/j.biomaterials.2010.01.140. Epub 2010 Feb 23.


DOI:10.1016/j.biomaterials.2010.01.140
PMID:20181393
Abstract

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 800 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 approximately 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 approximately 60-100, a non-instant, but progressive cell deterioration, is observed.

摘要

采用双光子激发的金纳米棒(AuNRs)原位实时观察活 EMT-6 乳腺癌细胞的光热解。细胞的形态和质膜通透性是这些现象的关键指标。采用种子介导法合成了纵横比为 3.92、纵向吸收峰在 800nm 的 AuNRs。纳米棒表面进一步用聚苯乙烯磺酸盐(PSS)修饰以提高生物相容性。所制备的纳米棒显示出优异的双光子光致发光成像。实时原位结果表明,细胞内的空穴是由 AuNRs 局部光热效应引发的热爆炸产生的。空化动力学与能量有关,负责质膜的穿孔或突然破裂。细胞治疗的能量阈值与每个细胞摄取的纳米棒数量显著相关。对于每个细胞约 10-30 个纳米棒的摄取量 N,发现大于 93mJ/cm(2)的有效能量通量 E 会导致细胞在很短的时间内以破碎的形式有效破坏。对于能量水平 E = 18mJ/cm(2),N 约为 60-100,观察到非即时但渐进的细胞恶化。

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