In Vivo Biodistribution and Toxicology of Carboxylated Graphene Quantum Dots

被引:447
作者
Nurunnabi, Md [1 ]
Khatun, Zehedina [2 ]
Huh, Kang Moo [4 ]
Park, Sung Young [3 ]
Lee, Dong Yun [5 ]
Cho, Kwang Jae [6 ]
Lee, Yong-kyu [1 ,3 ]
机构
[1] Korea Natl Univ Transportat, Dept Polymer Sci & Engn, Chungbuk 380702, South Korea
[2] Korea Natl Univ Transportat, Dept Green Bioengn, Chungbuk 380702, South Korea
[3] Korea Natl Univ Transportat, Dept Chem & Biol Engn, Chungbuk 380702, South Korea
[4] Chungnam Natl Univ, Dept Polymer Sci & Engn, Taejon 305764, South Korea
[5] Hanyang Univ, Dept Bioengn, Seoul 133791, South Korea
[6] Catholic Univ Korea, Dept Otolaryngol Head & Neck Surg, Coll Med Uijeongbu, St Marys Hosp, Kyonggi Do 480717, South Korea
基金
新加坡国家研究基金会;
关键词
graphene quantum dots; biodistribution; toxicity; imaging; serum biochemistry; ORAL DELIVERY; OXIDE; FUNCTIONALIZATION; PHOTOLUMINESCENCE; EFFICIENT; IMPROVES; SENSORS; PROBE;
D O I
10.1021/nn402043c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoluminescent graphene quantum dots (GQDs) have fascinating optical and electronic properties with numerous promising applications in biomedical engineering. In this work, we first studied the in vivo biodistribution and the potential toxicity of carboxylated photoluminescent GQDs. KB, MDA-MB231, A549 cancer cells, and MDCK (normal cell line were chosen as in vitro cell culture models to examine the possible adverse effects of the carboxylated photoluminescent GQDs. The carboxylated GQDs are desirable for increased aqueous solubility. All cancer cells efficiently took up the carboxylated GQDs. No acute toxicity or morphological changes were noted in either system at the tested exposure levels. A long-term in vivo study revealed that the GQDs mainly accumulated in liver, spleen, lung, kidney, and tumor sites after Intravenous injection. To reveal any potential toxic effect of the GQDs on treated mice, serum biochemical analysis and histological evaluation were performed. The toxicity results from serum biochemistry and complete blood count study revealed that the GQDs do not cause appreciable toxicity to the treated animals. Finally, we observed no obvious organ damage or lesions for the GQDS treated mice after 21 days of administration at 5 mg/kg or 10 mg/kg dosages. With adequate studies of toxicity, both in vitro and in vivo, photoluminescent GQDs may be considered for biological application.
引用
收藏
页码:6858 / 6867
页数:10
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