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Research ArticlePhysics/Instrumentation

In Vivo 3-Dimensional Radiopharmaceutical-Excited Fluorescence Tomography

Zhenhua Hu, Mingxuan Zhao, Yawei Qu, Xiaojun Zhang, Mingru Zhang, Muhan Liu, Hongbo Guo, Zeyu Zhang, Jing Wang, Weidong Yang and Jie Tian
Journal of Nuclear Medicine January 2017, 58 (1) 169-174; DOI: https://doi.org/10.2967/jnumed.116.180596
Zhenhua Hu
1Key Laboratory of Molecular Imaging of Chinese Academy of Sciences, Institute of Automation, Chinese Academy of Sciences, Beijing, China
2The State Key Laboratory of Management and Control for Complex Systems, Institute of Automation, Chinese Academy of Sciences, Beijing, China
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Mingxuan Zhao
3Department of Nuclear Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, China
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Yawei Qu
4Department of Gastroenterology, General Hospital of Chinese Armed Police Forces, Beijing, China; and
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Xiaojun Zhang
5Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing, China
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Mingru Zhang
3Department of Nuclear Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, China
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Muhan Liu
1Key Laboratory of Molecular Imaging of Chinese Academy of Sciences, Institute of Automation, Chinese Academy of Sciences, Beijing, China
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Hongbo Guo
1Key Laboratory of Molecular Imaging of Chinese Academy of Sciences, Institute of Automation, Chinese Academy of Sciences, Beijing, China
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Zeyu Zhang
1Key Laboratory of Molecular Imaging of Chinese Academy of Sciences, Institute of Automation, Chinese Academy of Sciences, Beijing, China
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Jing Wang
3Department of Nuclear Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, China
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Weidong Yang
3Department of Nuclear Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, China
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Jie Tian
1Key Laboratory of Molecular Imaging of Chinese Academy of Sciences, Institute of Automation, Chinese Academy of Sciences, Beijing, China
2The State Key Laboratory of Management and Control for Complex Systems, Institute of Automation, Chinese Academy of Sciences, Beijing, China
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  • FIGURE 1.
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    FIGURE 1.

    CLI of radiopharmaceuticals and REFI of mixture of radiopharmaceuticals and EO nanoparticles. (A) Optical image of EO nanoparticles. (B) CL images of radiopharmaceuticals, including Na99mTcO4, 68GaCl3, 18F-FDG, and Na131I, and REF image of mixture of EO nanoparticles and radiopharmaceuticals (left). Quantification analysis of CL signal and REF signal (right). Open field was used for collecting all light. (C) Quantification analysis of optical signal intensity, which was obtained through subtraction of Cerenkov luminescent intensity from optical signal intensity of mixture of radiopharmaceutical and EO nanoparticles. (D) CLI of 18F-FDG and REFI of mixture of 18F-FDG and EO nanoparticles (left) and quantification analysis (right).

  • FIGURE 2.
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    FIGURE 2.

    CLI and REFI of phantoms. (A) Cerenkov luminescence images of phantoms injected with 68Ga with radioactivity of 0.185 MBq. Depths of sources were 1, 2, 5, 7, and 8 mm. (B) Radioluminescent images of 1 mg of EO excited by 68Ga with radioactivity of 0.185 MBq. (C) Quantification comparison results of REFI and CLI. (D) Comparison of 3D reconstruction DEs of CLT and REFT.

  • FIGURE 3.
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    FIGURE 3.

    REFT and CLT of artificial source–implantation mouse models. (A) REFI (left) and CLI (right) of mice implanted with artificial sources. Position of implanted source was close to ventral surface of abdomen (first row), lesser curvature of stomach (second row), and dorsal surface of abdomen of mouse (third row). (B) Comparison of reconstruction results of REFT and CLT. DE = reconstructed distance error, which is defined as distance from real source position to reconstructed source position; DS = source depth from real source position to surface of mouse body. (C) Relationship between DE of REFT or CLT and depth of implanted sources.

  • FIGURE 4.
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    FIGURE 4.

    Small-animal PET, CLI, REFI, and REFT of mouse bearing HCC tumors. (A–D) Small-animal PET, CLI, REFI, and REFT of same mouse. (E) Axial, coronal, and sagittal view of reconstructed results of REFT. (F) Photograph of 3 tumors during operation on mouse (arrows). (G) Hematoxylin and eosin results of tumors.

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    TABLE 1

    Comparison of Detection Rates of REFT and PET

    Mouse no.Detection rate of REFT (%)Detection rate of PET (%)
    110033.3
    28060
    310050
    47525
    Mean88.7542.08
    SD13.1515.84

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Journal of Nuclear Medicine: 58 (1)
Journal of Nuclear Medicine
Vol. 58, Issue 1
January 1, 2017
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In Vivo 3-Dimensional Radiopharmaceutical-Excited Fluorescence Tomography
Zhenhua Hu, Mingxuan Zhao, Yawei Qu, Xiaojun Zhang, Mingru Zhang, Muhan Liu, Hongbo Guo, Zeyu Zhang, Jing Wang, Weidong Yang, Jie Tian
Journal of Nuclear Medicine Jan 2017, 58 (1) 169-174; DOI: 10.2967/jnumed.116.180596

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In Vivo 3-Dimensional Radiopharmaceutical-Excited Fluorescence Tomography
Zhenhua Hu, Mingxuan Zhao, Yawei Qu, Xiaojun Zhang, Mingru Zhang, Muhan Liu, Hongbo Guo, Zeyu Zhang, Jing Wang, Weidong Yang, Jie Tian
Journal of Nuclear Medicine Jan 2017, 58 (1) 169-174; DOI: 10.2967/jnumed.116.180596
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Keywords

  • radiopharmaceutical excitation fluorescence tomography (REFT)
  • Cerenkov Luminescence Imaging (CLI)
  • radionuclides
  • hepatocellular carcinoma (HCC)
  • PET
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