Investigation of Sub-100 nm Gold Nanoparticles for Laser-Induced Thermotherapy of Cancer

被引:38
|
作者
Leung, Jennifer P. [1 ]
Wu, Sherry [1 ]
Chou, Keng C. [1 ]
Signorell, Ruth [1 ,2 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[2] ETH, Phys Chem Lab, CH-8093 Zurich, Switzerland
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
gold nanorods; gold core-corona nanoparticles; hollow gold nanoshells; light scattering microscopy; prostate cancer; gene therapy; TO-HEAT CONVERSION; PROSTATE-CANCER; PHOTOTHERMAL THERAPY; OPTICAL-PROPERTIES; ANTISENSE OLIGONUCLEOTIDES; DIFFERENT SIZES; CELL-LINES; NANORODS; GROWTH; EXPRESSION;
D O I
10.3390/nano3010086
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Specialized gold nanostructures are of interest for the development of alternative treatment methods in medicine. Photothermal therapy combined with gene therapy that supports hyperthermia is proposed as a novel multimodal treatment method for prostate cancer. In this work, photothermal therapy using small (<100 nm) gold nanoparticles and near-infrared (NIR) laser irradiation combined with gene therapy targeting heat shock protein (HSP) 27 was investigated. A series of nanoparticles: nanoshells, nanorods, core-corona nanoparticles and hollow nanoshells, were synthesized and examined to compare their properties and suitability as photothermal agents. In vitro cellular uptake studies of the nanoparticles into prostate cancer cell lines were performed using light scattering microscopy to provide three-dimensional (3D) imaging. Small gold nanoshells (40 nm) displayed the greatest cellular uptake of the nanoparticles studied and were used in photothermal studies. Photothermal treatment of the cancer cell lines with laser irradiation at 800 nm at 4 W on a spot size of 4 mm (FWHM) for 6 or 10 min resulted in an increase in temperature of similar to 12 degrees C and decrease in cell viability of up to 70%. However, in vitro studies combining photothermal therapy with gene therapy targeting HSP27 did not result in additional sensitization of the prostate cancer cells to hyperthermia.
引用
收藏
页码:86 / 106
页数:21
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