4.7 Article

Development of 18F-Labeled Picolinamide Probes for PET Imaging of Malignant Melanoma

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 56, Issue 3, Pages 895-901

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm301740k

Keywords

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Funding

  1. Melanoma Research Alliance, National Cancer Institute (NCI) In Vivo Cellular Molecular Imaging Center (ICMIC) [P50 CA114747]
  2. Chinese Ministry of Science and Technology [2009DFB30040]

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Melanoma is an aggressive skin cancer with worldwide increasing incidence. Development of positron emission tomography (PET) probes for early detection of melanoma is critical for improving the survival rate of melanoma patients. In this research, F-18-picolinamide-based PET probes were prepared by direct radiofluorination of the bromopicolinamide precursors using no-carrier-added F-18-fluoride. The resulting probes, F-18-1, F-18-2 and F-18-3, were then evaluated in vivo by small animal PET imaging and biodistribution studies in C57BL/6 mice bearing B16F10 murine melanoma tumors. Noninvasive small animal PET studies demonstrated excellent tumor imaging contrasts for all probes, while F-18-2 showed higher tumor to muscle ratios than F-18-1 and F-18-3. Furthermore, F-18-2 demonstrated good in vivo stability as evidenced by the low bone uptake in biodistribution studies. Collectively, these findings suggest F-18-2 as a highly promising PET probe for translation into clinical detection of melanoma.

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