Molecular Imaging Program at Stanford, Department of Radiology and Bio-X Program, Stanford University, Stanford, California, United States of America.
PLoS One. 2010 Mar 1;5(3):e9470. doi: 10.1371/journal.pone.0009470.
Optical imaging (OI) techniques such as bioluminescence and fluorescence imaging have been widely used to track diseases in a non-invasive manner within living subjects. These techniques generally require bioluminescent and fluorescent probes. Here we demonstrate the feasibility of using radioactive probes for in vivo molecular OI.
METHODOLOGY/PRINCIPAL FINDINGS: By taking the advantages of low energy window of light (1.2-3.1 eV, 400-1000 nm) resulting from radiation, radionuclides that emit charged particles such as beta(+) and beta(-) can be successfully imaged with an OI instrument. In vivo optical images can be obtained for several radioactive probes including 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]FDG), Na(18)F, Na(131)I, (90)YCl(3) and a (90)Y labeled peptide that specifically target tumors.
CONCLUSIONS/SIGNIFICANCE: These studies demonstrate generalizability of radioactive OI technique. It provides a new molecular imaging strategy and will likely have significant impact on both small animal and clinical imaging.
光学成像(OI)技术,如生物发光和荧光成像,已被广泛用于在活体中以非侵入性的方式跟踪疾病。这些技术通常需要生物发光和荧光探针。在这里,我们展示了使用放射性探针进行体内分子 OI 的可行性。
方法/主要发现:通过利用辐射产生的低能量窗口光(1.2-3.1 eV,400-1000nm)的优势,可以使用 OI 仪器成功地对发射带电粒子(如β+和β-)的放射性核素进行成像。可以获得几种放射性探针的体内光学图像,包括 2-脱氧-2-[(18)F]氟-D-葡萄糖([(18)F]FDG)、Na(18)F、Na(131)I、(90)YCl(3)和一种专门针对肿瘤的(90)Y 标记肽。
结论/意义:这些研究证明了放射性 OI 技术的通用性。它提供了一种新的分子成像策略,可能对小动物和临床成像都有重大影响。