logo

Nanographene oxide labeling with 188Re

RADIOCHEMISTRY, RADIOPHARMACEUTICALS AND NUCLEAR MEDICINE

Nanographene oxide labeling with 188Re

ZHANG Xiaoyong
LI Jing
ZHU Ying
QI Yujin
ZHU Zhiyong
LI Wenxin
HUANG Qing
Nuclear Science and TechniquesVol.22, No.2pp.99-104Published in print 20 Apr 2011
36400

Nanographene oxide (NGO) is currently being explored for various biomedical applications. However, little information is known about its biological behaviors in vitro and in vivo. For further studying its pharmacokinetics and related biological behaviors in living systems, an effective and convenient tracing method is particularly demanded. In this work, NGO was labeled with radionuclide 188Re (188Re-NGO). To obtain high labeling yield and purity, a number of labeling conditions, including concentration of SnCl2 and ascorbic acid, reaction time and temperature, and pH were optimized, and stability of the 188Re-NGO in vitro and in vivo was evaluated. The results showed that NGO could be effectively labeled with high yield. The purified 188Re-NGO showed high stability in vitro and in vivo. A pretest of NGO biodistribution with single photon emission computed tomography showed that the 188Re-NGO was rapidly taken by organs such as lungs, liver, and spleen. The biodistribution of 188Re-NGO differs significantly from the free radionuclide, indicating that the labeling procedure is highly suitable for investigating its biological behavior in living systems.

Graphene oxideRadio-labeling188ReSPECT imagesBiodistribution
References
[1] Becerril H A, Mao J, Liu Z F, et al. ACS Nano, 2008, 2: 463-470.
[2] Gilje S, Han S, Wang M S, et al. Nano Lett, 2007, 7: 3394-3398.
[3] Stankovich S, Dikin D A, Dommett G H B, et al. Nature, 2006, 442: 282-286.
[4] Liu Z, Robinson J T, Sun X M, et al. J Am Chem Soc, 2008, 130: 10876-10877.
[5] Sun X M, Liu Z, Welsher K, et al. Nano Res, 2008, 1: 203-212.
[6] He S J, Song B, Li D, et al. Adv Funct Mater, 2010, 20: 453-459.
[7] Hong H, Gao T, Cai W B. Nano Today, 2009, 4: 252-261.
[8] Li Q N, Xiu Y, Zhang X D, et al. Nucl Med Biol, 2002, 29: 707-710.
[9] Wang H F, Wang J, Deng X Y, et al. J Nanosci Nanotechnol, 2004, 4: 1019-1024.
[10] Deng X Y, Yang S T, Nie H Y, et al. Nanotechnology, 2008, 19: 075101.
[11] Zinn Kurt R., Buchsbaum D J, Chaudhuri T R, et al. J Nucl Med, 2000, 41: 887-895.
[12] Hummers W S, Offeman R E. J Am Chem Soc, 1958, 80: 1339.
[13] Zhang X Y, Yin J L, Peng C, et al. Carbon, 2011, 49: 986-995.
[14] Zhang X Y, Yin J L, Kang C, et al. Toxicol Lett, 2010, 49: 237-243.
[15] Seifert S, Pietzsch H J. Appl Radiat Isot, 2006, 64: 223-227.
[16] Yang S T, Guo W, Lin Y, et al. J Phys Chem C, 2007, 111: 17761-17764.