Activation imaging of gold nanoparticles for versatile drug visualization: An <i>in vivo</i> demonstration

N N. Koshikawa (Graduate School of Advanced Science and Engineering, Waseda University 1 , Tokyo,) Y Y. Kikuchi K K. S. Tanaka (Waseda University 1 , Shinjuku, Tokyo 169-8555,) K K. Tokoi (Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,) A A. Mitsukai (Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,) H H. Aoto (Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,) Y Y. Kadonaga (Institute for Radiation Sciences, Osaka University 3 , Osaka,) A A. Toyoshima (Institute for Radiation Sciences, Osaka University 3 , Osaka,) H H. Kato (Institute for Radiation Sciences, Osaka University 3 , Osaka,) K K. Ooe (Institute for Radiation Sciences, Osaka University 3 , Osaka,) K K. Takamiya (Institute for Integrated Radiation and Nuclear Science, Kyoto University 4 , Kyoto,) J J. Kataoka (Waseda University 1 , Shinjuku, Tokyo 169-8555,)

Abstract

Gold nanoparticles (AuNPs) have recently attracted considerable attention as promising drug carriers. In vivo imaging of AuNPs is required to investigate their pharmacokinetics. However, a direct and highly sensitive method has not yet been established. Therefore, we proposed the activation imaging of AuNPs that radioactivates AuNPs and non-invasively visualizes them using the emitted gamma rays. When the stable isotope of gold, 197Au, is irradiated with low-energy neutrons, it changes to radioactive 198Au, which predominantly emits 412-keV gamma rays. In this study, we synthesized [198Au]AuNPs through neutron irradiation and intratumorally injected them into tumor-bearing mice. In vivo imaging was performed using wideband x rays and gamma rays imager, and the distribution of [198Au]AuNPs in the body of mice was observed. Furthermore, we labeled the alpha-emitting therapeutic drug 211At with [198Au]AuNPs. Although 211At itself can be visualized using its 79-keV x rays, the long-term tracking of 211At-labeled AuNPs has been challenging due to its relatively short half-life of 7.2 h. The activation of AuNPs enables the long-term tracking of 211At-labeled AuNPs owing to the 2.7-day half-life of 198Au. 211At-labeled [198Au]AuNPs were injected intravenously into mice and visualized using a wideband x rays and gamma rays imager. Simultaneous imaging of 211At and 198Au was performed on the day of injection and 2 days after injection. Although 211At could no longer be imaged 2 days after injection, the distribution of the drug was visualized using gamma rays from 198Au.

Article Details

Volume / Issue Vol. 126, Issue 10
Published March 10, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (12)

N

N. Koshikawa

Graduate School of Advanced Science and Engineering, Waseda University 1 , Tokyo,

Y

Y. Kikuchi

K

K. S. Tanaka

Waseda University 1 , Shinjuku, Tokyo 169-8555,

K

K. Tokoi

Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,

A

A. Mitsukai

Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,

H

H. Aoto

Department of Chemistry, Graduate School of Science, Osaka University 2 , Osaka,

Y

Y. Kadonaga

Institute for Radiation Sciences, Osaka University 3 , Osaka,

A

A. Toyoshima

Institute for Radiation Sciences, Osaka University 3 , Osaka,

H

H. Kato

Institute for Radiation Sciences, Osaka University 3 , Osaka,

K

K. Ooe

Institute for Radiation Sciences, Osaka University 3 , Osaka,

K

K. Takamiya

Institute for Integrated Radiation and Nuclear Science, Kyoto University 4 , Kyoto,

J

J. Kataoka

Waseda University 1 , Shinjuku, Tokyo 169-8555,