DOE OSTI2016
Nanomaterials are constantly used in several applications of science and engineering. Nanoparticles are currently utilized in computer circuits, clothes, luminescent devices, catalysis, medicine, among many others uses. In the clinical field nanomaterials have become an innovative alternative for early diagnosis and treatment of a significant number of medical conditions. Nanoparticles can be utilized in applications ranging from contrast agents for imaging purposes to carriers for drug delivery in cancerous tumors. The use of nanoparticles made of high atomic number elements as noble metals, is becoming an attractive approach for enhancing the radiation dose delivered to a tissue during radiation therapy. The enhancement effect that makes the cells more sensitive to radiation is known as radiosensitization. Materials such as gold (Au) and titanium dioxide (TiO{sub 2}) at the nanoscale have become promising radiosensitizers. When TiO{sub 2} is irradiated with high energy photons, electron-holes are created within the material. This species interacts with surrounding medium generating reactive oxygen species (ROS). ROS create a toxic environment for cancerous cells, ultimately causing their death. On the other hand gold has a different interaction with ionizing radiation. Upon radiation, gold releases a spray of secondary products such as photoelectrons, auger electrons, and characteristic X-rays. The energy created by the escaping electrons leads to DNA strands breaks in the cells causing their death. Therefore, if these nanoparticles are initially accumulated in the tissue to be treated, the dose delivered during radiation therapy is amplified. This represents a synergistic approach to enhance radiation therapy while substantially reducing side effects. Radiosensitization by nanoparticles often depends on their particle size, morphology and synthesis route. The most commonly used methods to synthesize metallic nanoparticles such as gold involves chemical reduction of a metal precursor. In this case, reducing agents are used in order to transform the metallic ions to metal atoms that will subsequently coalesce and grow to form the nanoparticles . Nevertheless there are alternative methods that do not require a chemical reducing agent. Radiation synthesis is one of those processes. The interaction of ionizing radiation with an aqueous solution containing a metal precursor, leads to a phenomena known as radiolysis of water. Radiolysis of water produces chemical species such as solvated electrons (e{sup -}{sub aq}), and hydrogen atoms (H{sup +}). These species are strong reducing agents that bring the metal ions existing in solution into stable metal atoms that will form nanoparticles. Radiation synthesis is a novel method that offers significant advantages over conventional approaches such as wet chemistry routes. In this approach, no further chemical reducing agents are needed, thus it does not generate byproducts that may affect the nanoparticles properties. This is particularly important in medical applications. Furthermore, this technique is designed to work at room temperature and under atmospheric pressures. Nonetheless the most outstanding feature of radiation synthesis is the possibility to control the particle size and size distribution. This route allows for narrow particle size distributions with size ranging from 2 to 30 nm. Furthermore, the availability of different ionizing radiation producing devices such as synchrotrons, X-ray irradiators, and gamma irradiators enables the possibility of manufacturing nanomaterials under various conditions. In this work, Au nanoparticles were deposited onto TiO{sub 2} using the radiation synthesis method. In addition, the radiosensitization characteristics of TiO{sub 2} and TiO{sub 2}/Au nanoparticles were evaluated through the decomposition of the organic dye Methylene Blue (MB). In order to analyze the degradation of the dye the TiO{sub 2} and TiO{sub 2}/Au nanoparticles were placed in an aqueous solution along with MB and subjected to X-ray irradiation. The samples were irradiated for 30 and 60 minutes. The degradation of the MB after irradiation in the presence and absence of the nanomaterials was measured by UV-Vis spectroscopy following the decrease in the absorbance of the dye at 664 nm. (authors)