Nanoscale energy deposition by x-ray absorbing nanostructures

被引:198
作者
Carter, Joshua D. [1 ]
Cheng, Neal N. [1 ]
Qu, Yongquan [1 ]
Suarez, George D. [1 ]
Guo, Ting [1 ]
机构
[1] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
关键词
DNA STRAND BREAKS; GOLD NANOPARTICLES; PHOTON-ACTIVATION; AUGER ELECTRONS; SINGLE-STRAND; RADIATION; WATER; SIZE; IODODEOXYURIDINE; RADICALS;
D O I
10.1021/jp075253u
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here we wish to demonstrate a unique property of nanomaterials: energy deposition with nanometer precision from low-energy electrons released from these nanostructures interacting with hard X-ray radiation in aqueous solution. Three effects combine to cause this phenomenon: (1) localized absorption of X-rays by nanostructures, (2) effective release of low-energy electrons from small nanostructures, and (3) efficient deposition of energy in water in the form of radicals and electrons. This combination creates localized X-ray absorption and localized energy deposition of nanometer precision. We confirmed the theoretically predicted nanoscale energy deposition distribution by measuring hydroxyl radical-induced DNA strand breaks, and observed enhanced damage to a 5600-bp DNA molecule from approximately 10 chemically conjugated small gold nanoparticles under X-ray radiation. These results provide a general guidance to applications of this new concept in many fields including radiation chemistry, radiology, radiation oncology, biochemistry, biology, and nanotechnology.
引用
收藏
页码:11622 / 11625
页数:4
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