Understanding Resonant Light-Triggered DNA Release from Plasmonic Nanoparticles

被引:92
|
作者
Goodman, Amanda M. [1 ]
Hogan, Nathaniel J. [2 ]
Gottheim, Samuel [1 ]
Li, Carrie [1 ]
Clare, Susan E. [5 ]
Halas, Naomi J. [1 ,2 ,3 ,4 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Dept Elect & Comp Engn, Houston, TX 77005 USA
[3] Rice Univ, Dept Phys & Astron, Houston, TX 77005 USA
[4] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Surg, Chicago, IL 60611 USA
基金
美国国家科学基金会;
关键词
nanoshells; DNA; laser; photothermal heating; oligonucleotide; NEAR-INFRARED LIGHT; REMOTE-CONTROLLED RELEASE; TARGETED DRUG-DELIVERY; GOLD NANOPARTICLES; RESPONSIVE NANOPARTICLES; PHOTOTHERMAL RELEASE; CANCER-TREATMENT; LIVING CELLS; NANOSHELLS; NANORODS;
D O I
10.1021/acsnano.6b06510
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoparticle-based platforms for gene therapy and drug delivery are gaining popularity for cancer treatment. To improve therapeutic selectivity, one important strategy is to remotely trigger the release of a therapeutic cargo from a specially designed gene- or drug-laden near-infrared (NIR) absorbing gold nanoparticle complex with NIR light. While there have been multiple demonstrations of NIR nanoparticle-based release platforms, our understanding of how light-triggered release works in such complexes is still limited. Here, we investigate the specific mechanisms of DNA release from plasmonic nanoparticle complexes using continuous wave (CW) and femtosecond pulsed lasers. We find that the characteristics of nanoparticle-based DNA release vary profoundly from the same nanoparticle complex, depending on the type of laser excitation. CW laser illumination drives the photothermal release of dehybridized single-stranded DNA, while pulsed-laser excitation results in double stranded DNA release by cleavage of the Au-S bond, with negligible local heating. This dramatic difference in DNA release from the same DNA-nanoparticle complex has very important implications in the development of NIR-triggered gene or drug delivery nanocomplexes.
引用
收藏
页码:171 / 179
页数:9
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