Combining Portable Raman Probes with Nanotubes for Theranostic Applications

被引:32
作者
Bhirde, Ashwinkumar A. [1 ]
Liu, Gang [1 ]
Jin, Albert [2 ]
Iglesias-Bartolome, Ramiro [3 ]
Sousa, Alioscka A. [2 ]
Leapman, Richard D. [2 ]
Gutkind, J. Silvio [3 ]
Lee, Seulki [1 ]
Chen, Xiaoyuan [1 ]
机构
[1] NIBIB, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
[2] NIBIB, Lab Cellular Imaging & Macromol Biophys, NIH, Bethesda, MD 20892 USA
[3] NIDCR, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
来源
THERANOSTICS | 2011年 / 1卷
基金
美国国家卫生研究院;
关键词
Irradiation; Raman; photothermal; multi-walled carbon nanotube (MWCNT); single-walled carbon nanotube (SWCNT); 3D cell culture; WALLED CARBON NANOTUBES; IN-VIVO; DRUG-DELIVERY; CANCER; OPPORTUNITIES; SPECTROSCOPY; NANOMATERIALS; CHALLENGES; DISPERSION; BIOLOGY;
D O I
10.7150/thno/v01p0310
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recently portable Raman probes have emerged along with a variety of applications, including carbon nanotube (CNT) characterization. Aqueous dispersed CNTs have shown promise for biomedical applications such as drug/gene delivery vectors, photo-thermal therapy, and photoacoustic imaging. In this study we report the simultaneous detection and irradiation of carbon nanotubes in 2D monolayers of cancer cells and in 3D spheroids using a portable Raman probe. A portable handheld Raman instrument was utilized for dual purposes: as a CNT detector and as an irradiating laser source. Single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs) were dispersed aqueously using a lipid-polymer (LP) coating, which formed highly stable dispersions both in buffer and cell media. The LP coated SWCNT and MWCNT aqueous dispersions were characterized by atomic force microscopy, transmission electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy and Raman spectroscopy. The cellular uptake of the LP-dispersed SWCNTs and MWCNTs was observed using confocal microscopy, and fluorescein isothiocyanate (FITC)-nanotube conjugates were found to be internalized by ovarian cancer cells by using Z-stack fluorescence confocal imaging. Biocompatibility of SWCNTs and MWCNTs was assessed using a cell viability MTT assay, which showed that the nanotube dispersions did not hinder the proliferation of ovarian cancer cells at the dosage tested. Ovarian cancer cells treated with SWCNTs and MWCNTs were simultaneously detected and irradiated live in 2D layers of cancer cells and in 3D environments using the portable Raman probe. An apoptotic terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay carried out after laser irradiation confirmed that cell death occurred only in the presence of nanotube dispersions. We show for the first time that both SWCNTs and MWCNTs can be selectively irradiated and detected in cancer cells using a simple handheld Raman instrument. This approach could potentially be used to treat various diseases, including cancer.
引用
收藏
页码:310 / 321
页数:12
相关论文
共 48 条
  • [1] Synthesis and Characterization of a Carbon Nanotube-Dendron Series for Efficient siRNA Delivery
    Antonia Herrero, M.
    Toma, Francesca M.
    Al-Jamal, Khuloud T.
    Kostarelos, Kostas
    Bianco, Alberto
    Da Ros, Tatiana
    Bano, Fouzia
    Casalis, Loredana
    Scoles, Giacinto
    Prato, Maurizio
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (28) : 9843 - 9848
  • [2] The biology of ovarian cancer: new opportunities for translation
    Bast, Robert C., Jr.
    Hennessy, Bryan
    Mills, Gordon B.
    [J]. NATURE REVIEWS CANCER, 2009, 9 (06) : 415 - 428
  • [3] Distribution and clearance of PEG-single-walled carbon nanotube cancer drug delivery vehicles in mice
    Bhirde, Ashwin A.
    Patel, Sachin
    Sousa, Alioscka A.
    Patel, Vyomesh
    Molinolo, Alfredo A.
    Ji, Youngmi
    Leapman, Richard D.
    Gutkind, J. Silvio
    Rusling, James F.
    [J]. NANOMEDICINE, 2010, 5 (10) : 1535 - 1546
  • [4] Bhirde AA, 2009, NANOMEDICINE-UK, V4, P763, DOI [10.2217/nnm.09.56, 10.2217/NNM.09.56]
  • [5] Targeted Killing of Cancer Cells in Vivo and in Vitro with EGF-Directed Carbon Nanotube-Based Drug Delivery
    Bhirde, Ashwin A.
    Patel, Vyomesh
    Gavard, Julie
    Zhang, Guofeng
    Sousa, Alioscka A.
    Masedunskas, Andrius
    Leapman, Richard D.
    Weigert, Roberto
    Gutkind, J. Silvio
    Rusling, James F.
    [J]. ACS NANO, 2009, 3 (02) : 307 - 316
  • [6] Nanoparticles for cell labeling
    Bhirde, Ashwinkumar
    Xie, Jin
    Swierczewska, Maggie
    Chen, Xiaoyuan
    [J]. NANOSCALE, 2011, 3 (01) : 142 - 153
  • [7] Opportunities and challenges of carbon-based nanomaterials for cancer therapy
    Bianco, Alberto
    Kostarelos, Kostas
    Prato, Maurizio
    [J]. EXPERT OPINION ON DRUG DELIVERY, 2008, 5 (03) : 331 - 342
  • [8] CHROMOPHORE-ENHANCED LASER-TUMOR TISSUE PHOTOTHERMAL INTERACTION USING AN 808-NM DIODE-LASER
    CHEN, WR
    ADAMS, RL
    HEATON, S
    DICKEY, DT
    BARTELS, KE
    NORDQUIST, RE
    [J]. CANCER LETTERS, 1995, 88 (01) : 15 - 19
  • [9] Costa S, 2008, MATER SCI-POLAND, V26, P433
  • [10] Molecular Profiling Uncovers a p53-Associated Role for MicroRNA-31 in Inhibiting the Proliferation of Serous Ovarian Carcinomas and Other Cancers
    Creighton, Chad J.
    Fountain, Michael D.
    Yu, Zhifeng
    Nagaraja, Ankur K.
    Zhu, Huifeng
    Khan, Mahjabeen
    Olokpa, Emuejevoke
    Zariff, Azam
    Gunaratne, Preethi H.
    Matzuk, Martin M.
    Anderson, Matthew L.
    [J]. CANCER RESEARCH, 2010, 70 (05) : 1906 - 1915