Author/Authors :
Xia, Yuxiao Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Zhang, Li Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Zhao, Yanhong Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Liu, Xiangdong Department of Hepatobiliary Surgery - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Cai, Liang Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Liu, Lin Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Chen, Yue Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China , Zhang, Wei Department of Nuclear Medicine - Affiliated Hospital of Southwest Medical University - Luzhou - Sichuan, China
Abstract :
This work evaluated the potential of 68Ga-labelledNOTA-ICG (1,4,7-triazacyclononane-1,4,7-triacetic acid indocyanine
green) for liver reserve imaging. Methods. To determine the optimal conditions for generating 68Ga-NOTA-ICG, various reaction
parameters were implemented. Quality control analysis was performed using different chromatography techniques. The in vitro
and in vivo stability was also measured at specific time points. The radioactivity ratio between n-octanol and water was determined
to evaluate the water solubility of 68Ga-NOTA-ICG. The plasma-protein binding rate of the labelled compound was determined by
the methanol method. The biodistribution and imaging findings were evaluated in normal animals at different time points after
injection. A preliminary imaging evaluation was performed using an animal model of hepatic ischaemia-reperfusion injury, which
was confirmed by pathology. Results. 68Ga-NOTA-ICG was prepared with very high radiochemical purity (>98%) by reacting at
90°C for 10 min at pH = 3.5∼4.0, with excellent stability in vivo and in vitro (>95% 3 h postpreparation). The in vitro plasmaprotein binding rate of 68Ga-NOTA-ICG was 13.01 ± 0.7%, and it showed strong water solubility (log P = −2.01 ± 0.04). We
found that in addition to excretion through the biliary tract and intestines, 68Ga-NOTA-ICG can be excreted through the urinary
tract. The image quality of 68Ga-NOTA-ICG was very high; imaging agent retained in the area of liver injury could clearly be
observed. Conclusion. This is the first report on a 68Ga-labelled NOTA-ICG fragment for liver reserve function studies. This
complex has promise as a candidate agent for liver reserve imaging.
Keywords :
tricarboxycyanine , FDA , ICG , HPLC