Dose enhancement effects to the nucleus and mitochondria from gold nanoparticles in the cytosol
Creators
- 1. Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, 30 Fruit St, Boston, MA 02114 (United States)
- 2. Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW 2234 (Australia)
- 3. School of Physics, University of Sydney, NSW 2006 (Australia)
Description
Gold nanoparticles (GNPs) have shown potential as dose enhancers for radiation therapy. Since damage to the genome affects the viability of a cell, it is generally assumed that GNPs have to localise within the cell nucleus. In practice, however, GNPs tend to localise in the cytoplasm yet still appear to have a dose enhancing effect on the cell. Whether this effect can be attributed to stress-induced biological mechanisms or to physical damage to extra-nuclear cellular targets is still unclear. There is however growing evidence to suggest that the cellular response to radiation can also be influenced by indirect processes induced when the nucleus is not directly targeted by radiation. The mitochondrion in particular may be an effective extra-nuclear radiation target given its many important functional roles in the cell. To more accurately predict the physical effect of radiation within different cell organelles, we measured the full chemical composition of a whole human lymphocytic JURKAT cell as well as two separate organelles; the cell nucleus and the mitochondrion. The experimental measurements found that all three biological materials had similar ionisation energies ∼70 eV, substantially lower than that of liquid water ∼78 eV. Monte Carlo simulations for 10–50 keV incident photons showed higher energy deposition and ionisation numbers in the cell and organelle materials compared to liquid water. Adding a 1% mass fraction of gold to each material increased the energy deposition by a factor of ∼1.8 when averaged over all incident photon energies. Simulations of a realistic compartmentalised cell show that the presence of gold in the cytosol increases the energy deposition in the mitochondrial volume more than within the nuclear volume. We find this is due to sub-micron delocalisation of energy by photoelectrons, making the mitochondria a potentially viable indirect radiation target for GNPs that localise to the cytosol. (paper)
Availability note (English)
Available from http://dx.doi.org/10.1088/0031-9155/61/16/5993Additional details
Identifiers
Publishing Information
- Journal Title
- Physics in Medicine and Biology
- Journal Volume
- 61
- Journal Issue
- 16
- Journal Page Range
- p. 5993-6010
- ISSN
- 0031-9155
- CODEN
- PHMBA7
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49090803
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE; S61: RADIATION PROTECTION AND DOSIMETRY;
- Descriptors DEI
- CELL NUCLEI; COMPUTERIZED SIMULATION; CYTOPLASM; DAMAGE; ENERGY ABSORPTION; ENERGY LOSSES; MITOCHONDRIA; MONTE CARLO METHOD; NANOPARTICLES; RADIATION DOSES; RADIOTHERAPY
- Descriptors DEC
- ABSORPTION; CALCULATION METHODS; CELL CONSTITUENTS; DOSES; LOSSES; MEDICINE; NUCLEAR MEDICINE; PARTICLES; RADIOLOGY; SIMULATION; SORPTION; THERAPY