Facile Synthesis of Biocompatible Amine Oxide Grafted Fullerene and Its Antioxidant Performances without Metal Loading

Yuxuan Xiaa, Jiaxin Maa, Jiayao Zhenga, Ziyi Lua, Qiong Zhanga, Baowei Lia, Siyu Chena, Dongmei Lia, Qiang Zhangb, Liu Honga, *, Bingtian Zhaoa, **, and Cheng Yanga

aKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122 China

bSchool of Chemistry and Life Sciences, Suzhou University of Science and Technology, Suzhou, 215009 China

email: *hongliu@jiangnan.edu.cn
email: **btzhao@jiangnan.edu.cn

Received 5 August, 2022

Abstract— Fullerene (C60) has been regarded as an effective radical scavenger for many years, but the highly hydrophobic nature strongly limits its application in biological fields. Herein, a simple and green strategy for synthesizing water-soluble fullerene derivative was reported, in which intrinsic C60 was grafted by amine oxide functional group (AO-C60). In addition to its excellent aqueous dispersion, AO-C60 exhibited extremely low toxicity to mice macrophage cell RAW264.7. Further experiments have confirmed the prominent antioxidative ability of AO-C60 towards typical free radicals including 1,1-diphenyl-2-picrylhydrazy (DPPH) radical, hydroxyl radical (OH) and nitric oxide (NO) without the help of metal loading, while the IC50 could be as low as 0.09 mg/mL. Our work will shed light on the development of anti-oxidative nanoagents with both effectiveness and bio-safety.

Keywords: fullerene, amino oxide, radical scavenging, biocompatibility

DOI: 10.1134/S1070363222110238