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In Vivo Pharmacokinetics, Long-Term Biodistribution, and Toxicology of PEGylated Graphene in Mice

机译:小鼠体内PEG化石墨烯的体内药代动力学,长期生物分布和毒理学

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摘要

Graphene has emerged as interesting nanomaterials with promising applications in a range of fields including biomedicine. In this work, for the first time we study the long-term in vivo biodistribution of ~(125)I-labeled nanographene sheets (NGS) functionalized with polyethylene glycol (PEG) and systematically examine the potential toxicity of graphene over time. Our results show that PEGylated NGS mainly accumulate in the reticuloendothelial system (RES) including liver and spleen after intravenous administration and can be gradually cleared, likely by both renal and fecal excretion. PEGylated NGS do not cause appreciable toxicity at our tested dose (20 mg/kg) to the treated mice in a period of 3 months as evidenced by blood biochemistry, hematological analysis, and histological examinations. Our work greatly encourages further studies of graphene for biomedical applications.
机译:石墨烯已经成为有趣的纳米材料,并在包括生物医学在内的许多领域中具有广阔的应用前景。在这项工作中,我们第一次研究了用聚乙二醇(PEG)功能化的〜(125)I标记的纳米石墨烯片(NGS)的长期体内生物分布,并系统地研究了石墨烯随时间的潜在毒性。我们的研究结果表明,静脉给药后,聚乙二醇化的NGS主要积累在网状内皮系统(RES)中,包括肝脏和脾脏,并且可能逐渐被清除,可能通过肾脏和粪便排出。血液生化,血液学分析和组织学检查证明,聚乙二醇化NGS在我们测试的剂量(20 mg / kg)下在3个月内不会对小鼠产生明显的毒性。我们的工作极大地鼓励了石墨烯在生物医学领域的进一步研究。

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