TY - JOUR
T1 - Quantitative imaging of gold nanoparticle distribution in a tumor-bearing mouse using benchtop x-ray fluorescence computed tomography
AU - Manohar, Nivedh
AU - Reynoso, Francisco J.
AU - Diagaradjane, Parmeswaran
AU - Krishnan, Sunil
AU - Cho, Sang Hyun
N1 - Funding Information:
This investigation was supported by the NIH/NCI under award numbers R01CA155446, P30-CA016672-31, and 5U24-CA126577-0. The content is solely the responsibility of the authors and does not necessarily represent the official views of the US National Institutes of Health. The authors acknowledge the following people at The University of Texas MD Anderson Cancer Center: Mr. Charles Kingsley from the Small Animal Imaging Facility for help with cone beam CT imaging and Mr. Arthur Gelmis from the Department of Scientific Publications for his editorial help. The authors also acknowledge Dr. Yongjun Gao at University of Houston ICP Analytical Laboratory & Agilent Facility Center for help with ICP-MS analysis.
PY - 2016/2/25
Y1 - 2016/2/25
N2 - X-ray fluorescence computed tomography (XFCT) is a technique that can identify, quantify, and locate elements within objects by detecting x-ray fluorescence (characteristic x-rays) stimulated by an excitation source, typically derived from a synchrotron. However, the use of a synchrotron limits practicality and accessibility of XFCT for routine biomedical imaging applications. Therefore, we have developed the ability to perform XFCT on a benchtop setting with ordinary polychromatic x-ray sources. Here, we report our postmortem study that demonstrates the use of benchtop XFCT to accurately image the distribution of gold nanoparticles (GNPs) injected into a tumor-bearing mouse. The distribution of GNPs as determined by benchtop XFCT was validated using inductively coupled plasma mass spectrometry. This investigation shows drastically enhanced sensitivity and specificity of GNP detection and quantification with benchtop XFCT, up to two orders of magnitude better than conventional x-ray CT. The results also reaffirm the unique capabilities of benchtop XFCT for simultaneous determination of the spatial distribution and concentration of nonradioactive metallic probes, such as GNPs, within the context of small animal imaging. Overall, this investigation identifies a clear path toward in vivo molecular imaging using benchtop XFCT techniques in conjunction with GNPs and other metallic probes.
AB - X-ray fluorescence computed tomography (XFCT) is a technique that can identify, quantify, and locate elements within objects by detecting x-ray fluorescence (characteristic x-rays) stimulated by an excitation source, typically derived from a synchrotron. However, the use of a synchrotron limits practicality and accessibility of XFCT for routine biomedical imaging applications. Therefore, we have developed the ability to perform XFCT on a benchtop setting with ordinary polychromatic x-ray sources. Here, we report our postmortem study that demonstrates the use of benchtop XFCT to accurately image the distribution of gold nanoparticles (GNPs) injected into a tumor-bearing mouse. The distribution of GNPs as determined by benchtop XFCT was validated using inductively coupled plasma mass spectrometry. This investigation shows drastically enhanced sensitivity and specificity of GNP detection and quantification with benchtop XFCT, up to two orders of magnitude better than conventional x-ray CT. The results also reaffirm the unique capabilities of benchtop XFCT for simultaneous determination of the spatial distribution and concentration of nonradioactive metallic probes, such as GNPs, within the context of small animal imaging. Overall, this investigation identifies a clear path toward in vivo molecular imaging using benchtop XFCT techniques in conjunction with GNPs and other metallic probes.
UR - http://www.scopus.com/inward/record.url?scp=84959418910&partnerID=8YFLogxK
U2 - 10.1038/srep22079
DO - 10.1038/srep22079
M3 - Article
C2 - 26912068
AN - SCOPUS:84959418910
SN - 2045-2322
VL - 6
JO - Scientific reports
JF - Scientific reports
M1 - 22079
ER -