Abstract
Purpose
The purpose of this study was to quantify the microscopic dose distribution surrounding gold nanoparticles (GNPs) irradiated at therapeutic energies and to measure the changes in cell survival in vitro caused by this dose enhancement.
Methods
The dose distributions from secondary electrons surrounding a single gold nanosphere and single gold nanocube of equal volume were both simulated using MCNP6. Dose enhancement factors (DEFs) in the 1 μm3 volume surrounding a GNP were calculated and compared between a nanosphere and nanocube and between 6 and 18 MV energies. This microscopic effect was explored further by experimentally measuring the cell survival of C-33a cervical cancer cells irradiated at 18 MV with varying doses of energy and concentrations of GNPs. Survival of cells receiving no irradiation, a 3 Gy dose, and a 6 Gy dose of 18 MV energy were determined for each concentration of GNPs.
Results
It was observed that the dose from electrons surrounding the gold nanocube surpasses that of a gold nanosphere up to a distance of 1.1 μm by 18.5% for the 18 MV energy spectrum and by 23.1% for the 6 MV spectrum. DEFs ranging from ∼2 to 8 were found, with the maximum DEF resulting from the case of the gold nanocube irradiated at 6 MV energy. Experimentally, for irradiation at 18 MV, incubating cells with 6 nM (0.10% gold by mass) GNPs produces an average 6.7% decrease in cell survival, and incubating cells with 9 nM (0.15% gold by mass) GNPs produces an average 14.6% decrease in cell survival, as compared to cells incubated and irradiated without GNPs.
Conclusion
We have successfully demonstrated the potential radiation dose enhancing effects in vitro and microdosimetrically from gold nanoparticles.
Acknowledgments
The authors would like to thank Dr. Kelly Nash at the University of Texas at San Antonio for all of her advice on cell culture and cell survival assays. The authors would also like to thank Alejandro Morales Betancourt for his assistance involving lab equipment for cell culture and cell culture supplies as well as all of his advice on cell culture care. The authors acknowledge the University of Texas at San Antonio Kleberg Advanced Microscopy Center for support during this work.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Additional information
Funding
Notes on contributors
Tara M. Gray
Tara M. Gray recently received her Ph.D. in Physics from the University of Texas at San Antonio after receiving her master’s degree in Medical Physics from the University of Toledo. She currently works at the Cleveland Clinic in Cleveland, Ohio as a Resident in Therapeutic Medical Physics.
Shaquan David
Shaquan David is a doctoral candidate in the Department of Physics and Astronomy at the University of Texas at San Antonio.
Nema Bassiri
Nema Bassiri obtained his Ph.D. from the University of Texas Health Science Center at San Antonio. He currently works as a medical physics resident at the University of California, Davis.
Devanshi Yogeshkumar Patel
Devanshi Yogeshkumar Patel is an undergraduate researcher at the University of Texas at San Antonio.
Neil Kirby
Neil Kirby is an associate professor in the Department of Radiation Oncology at the University of Texas Health Science Center at San Antonio.
Kathryn M. Mayer
Kathryn M. Mayer is an associate professor in the Department of Physics and Astronomy at the University of Texas at San Antonio.