Protection from radiation-induced pneumonitis using cerium oxide nanoparticles

被引:289
作者
Colon, Jimmie [1 ]
Herrera, Luis [2 ]
Smith, Joshua [1 ]
Patil, Swanand [4 ]
Komanski, Chris [1 ]
Kupelian, Patrick [3 ]
Seal, Sudipta [4 ,5 ]
Jenkins, D. Wayne [3 ]
Baker, Cheryl H. [1 ,6 ]
机构
[1] MD Anderson Canc Ctr, Canc Res Inst, Orlando, FL 32806 USA
[2] MD Anderson Canc Ctr, Dept Thorac Surg, Orlando, FL 32806 USA
[3] MD Anderson Canc Ctr, Dept Radiat Oncol, Orlando, FL 32806 USA
[4] Univ Cent Florida, Dept Mech Mat & Aerosp Engn, AMPAC, Orlando, FL 32816 USA
[5] Univ Cent Florida, Nanosci & Technol Ctr, Orlando, FL 32816 USA
[6] Univ Cent Florida, Burnett Sch Biomed Sci, Orlando, FL 32816 USA
基金
美国国家科学基金会;
关键词
Radioprotection; Nanoparticles; Pneumonitis; Quality of life;
D O I
10.1016/j.nano.2008.10.003
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
In an effort to combat the harmful effects of radiation exposure, we propose that rare-earth cerium oxide (CeO2) nanoparticles (free-radical scavengers) protect normal tissue from radiation-induced damage. Preliminary studies suggest that these nanoparticles may be a therapeutic regenerative nanomedicine that will scavenge reactive oxygen species, which are responsible for radiation-induced cell damage. The effectiveness of CeO2 nanoparticles in radiation protection in murine models during high-dose radiation exposure is investigated, with the ultimate goal of offering a new approach to radiation protection, using nanotechnology. We show that CeO2 nanoparticles are well tolerated by live animals, and they prevent the onset of radiation-induced pneumonitis when delivered to live animals exposed to high doses of radiation. In the end, these studies provide a tremendous potential for radioprotection and can lead to significant benefits for the preservation of human health and the quality of life for humans receiving radiation therapy. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:225 / 231
页数:7
相关论文
共 19 条
[1]
The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[2]
In vitro cytotoxicity of oxide nanoparticles: Comparison to asbestos, silica, and the effect of particle solubility [J].
Brunner, Tobias J. ;
Wick, Peter ;
Manser, Pius ;
Spohn, Philipp ;
Grass, Robert N. ;
Limbach, Ludwig K. ;
Bruinink, Arie ;
Stark, Wendelin J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (14) :4374-4381
[3]
Rare earth nanoparticles prevent retinal degeneration induced by intracellular peroxides [J].
Chen, Junping ;
Patil, Swanand ;
Seal, Sudipta ;
McGinnis, James F. .
NATURE NANOTECHNOLOGY, 2006, 1 (02) :142-150
[4]
How does radiation kill cells? [J].
Cohen-Jonathan, E ;
Bernhard, EJ ;
McKenna, WG .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (01) :77-83
[5]
Auto-catalytic ceria nanoparticles offer neuroprotection to adult rat spinal cord neurons [J].
Das, Mainak ;
Patil, Swanand ;
Bhargava, Neelima ;
Kang, Jung-Fong ;
Riedel, Lisa M. ;
Seal, Sudipta ;
Hickman, James J. .
BIOMATERIALS, 2007, 28 (10) :1918-1925
[6]
[60]Fullerene is a powerful antioxidant in vivo with no acute or subacute toxicity [J].
Gharbi, N ;
Pressac, M ;
Hadchouel, M ;
Szwarc, H ;
Wilson, SR ;
Moussa, F .
NANO LETTERS, 2005, 5 (12) :2578-2585
[7]
The role of cerium redox state in the SOD mimetic activity of nanoceria [J].
Heckert, Eric G. ;
Karakoti, Ajay S. ;
Seal, Sudipta ;
Self, William T. .
BIOMATERIALS, 2008, 29 (18) :2705-2709
[8]
α-Tocopherol and Atherosclerosis [J].
Kaul, N ;
Devaraj, S ;
Jialal, I .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2001, 226 (01) :5-12
[9]
Antioxidant vitamins and prevention of cardiovascular disease: Epidemiological and clinical trial data [J].
Marchioli, R ;
Schweiger, C ;
Levantesi, G ;
Tavazzi, L ;
Valagussa, F .
LIPIDS, 2001, 36 :S53-S63
[10]
Mechanisms of dysfunction of the nitric oxide pathway in vascular diseases [J].
Maxwell, AJ .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2002, 6 (02) :101-124