Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy

被引:314
作者
Lu, Wentong [1 ]
Singh, Anant Kumar [1 ]
Khan, Sadia Afrin [1 ]
Senapati, Dulal [1 ]
Yu, Hongtao [1 ]
Ray, Paresh Chandra [1 ]
机构
[1] Jackson State Univ, Dept Chem, Jackson, MS 39217 USA
关键词
ENERGY TRANSFER; NANOPARTICLES; SCATTERING; DNA; RELEASE; IDENTIFICATION; NANOCRYSTALS; BACTERIA; ANTIGEN; PROBES;
D O I
10.1021/ja104924b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prostate cancer is the second leading cause of cancer-related death among the American male population, and the cost of treating prostate cancer patients is about $10 billion/year in the United States. Current treatments are mostly ineffective against advanced-stage prostate cancer and are often associated with severe side effects. Driven by these factors, we report a multifunctional, nanotechnology-driven, gold nano-popcorn-based surface-enhanced Raman scattering (SERS) assay for targeted sensing, nanotherapy treatment, and in situ monitoring of photothermal nanotherapy response during the therapy process. Our experimental data show that, in the presence of LNCaP human prostate cancer cells, multifunctional popcorn-shaped gold nanoparticles form several hot spots and provide a significant enhancement of the Raman signal intensity by several orders of magnitude (2.5 x 10(9)). As a result, it can recognize human prostate cancer cells at the 50-cells level. Our results indicate that the localized heating that occurs during near-infrared irradiation can cause irreparable cellular damage to the prostate cancer cells. Our in situ time-dependent results demonstrate for the first time that, by monitoring SERS intensity changes, one can monitor photothermal nanotherapy response during the therapy process. Possible mechanisms and operating principles of our SERS assay are discussed. Ultimately, this nanotechnology-driven assay could have enormous potential applications in rapid, on-site targeted sensing, nanotherapy treatment, and monitoring of the nanotherapy process, which are critical to providing effective treatment of cancer.
引用
收藏
页码:18103 / 18114
页数:12
相关论文
共 59 条
[1]   Photoregulated Release of Caged Anticancer Drugs from Gold Nanoparticles [J].
Agasti, Sarit S. ;
Chompoosor, Apiwat ;
You, Chang-Cheng ;
Ghosh, Partha ;
Kim, Chae Kyu ;
Rotello, Vincent M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (16) :5728-+
[2]   Surface-enhanced Raman spectroscopy of DNA [J].
Barhoumi, Aoune ;
Zhang, Dongmao ;
Tam, Felicia ;
Halas, Naomi J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (16) :5523-5529
[3]   Detection of sequence-specific protein-DNA interactions via surface enhanced resonance Raman scattering [J].
Bonham, Andrew J. ;
Braun, Gary ;
Pavel, Ioana ;
Moskovits, Martin ;
Reich, Norbert O. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (47) :14572-+
[4]   Predicting the future burden of cancer [J].
Bray, F ;
Moller, B .
NATURE REVIEWS CANCER, 2006, 6 (01) :63-74
[5]   Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin [J].
Brown, Sarah D. ;
Nativo, Paola ;
Smith, Jo-Ann ;
Stirling, David ;
Edwards, Paul R. ;
Venugopal, Balaji ;
Flint, David J. ;
Plumb, Jane A. ;
Graham, Duncan ;
Wheate, Nial J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (13) :4678-4684
[6]   Noble Metal Nanocrystals: Plasmon Electron Transfer Photochemistry and Single-Molecule Raman Spectroscopy [J].
Brus, Louis .
ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (12) :1742-1749
[7]   Probing the structure of single-molecule surface-enhanced Raman scattering hot spots [J].
Camden, Jon P. ;
Dieringer, Jon A. ;
Wang, Yingmin ;
Masiello, David J. ;
Marks, Lawrence D. ;
Schatz, George C. ;
Van Duyne, Richard P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (38) :12616-+
[8]   Controlled Plasmonic Nanostructures for Surface-Enhanced Spectroscopy and Sensing [J].
Camden, Jon P. ;
Dieringer, Jon A. ;
Zhao, Jing ;
Van Duyne, Richard P. .
ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (12) :1653-1661
[9]   Synergistically Integrated Nanoparticles as Multimodal Probes for Nanobiotechnology [J].
Cheon, Jinwoo ;
Lee, Jae-Hyun .
ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (12) :1630-1640
[10]  
Chikezie O., 2010, J CANC, V1, P150