Author/Authors :
Ma, Xiaohong Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Wang, Shuang Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Hu, Longbin Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Feng, Shichao Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Wu, Zhiyuan Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Liu, Siyun Healthcare (China) - Beijing, China , Duan, Shaofeng Healthcare (China) - Beijing, China , Chen, Zhongwei Healthcare (China) - Beijing, China , Zhou, Chunwu Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China , Zhao, Xinming Cancer Hospital - Chinese Academy of Medical Sciences & Peking union Medical College - Beijing, China
Abstract :
Iron nanoparticles have an increasingly more and more important role in MR molecular imaging due to their novel magnetic and
surface chemical properties. They provide new possibilities for noninvasive diagnosis and treatment monitoring, especially for
tissues that are rich in macrophages. e smaller size and prolongation of the plasma half-life change the in vivo fate of ultrasmall
superparamagnetic iron oxide (USPIO) nanoparticles captured by liver in reticuloendothelial system (RES) or mononuclear
phagocytic system (MPS). However, there is still a lack of MR imaging studies on the liver assessing USPIO nanoparticles <5 nm in
size to reflect its absorption and clearance properties. In this study, we used MRI to study the in vitro phantom and in vivo rat liver
imaging characteristics of USPIO nanoparticles (<5 nm). e results showed that USPIO nanoparticles (<5 nm) could potentially
reduce longitudinal and transverse relaxation times and showed similar T1 relaxation rates compared with commercial gadolinium chelates. In addition, USPIO nanoparticles (<5 nm) in vivo demonstrated both positive (T1) and negative (T2) liver contrast
enhancement in healthy rats’ liver. Furthermore, USPIO nanoparticles showed relatively good in vitro biocompatibility and fast
clearance (within 45.17 minutes after intravenous injection) in the normal liver. Taken together, these data might inspire a new
personalized and precise diagnostic tool and stimulate new applications for specific targeted molecular probes.