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羧基化石墨烯量子点的体内生物分布和毒理学研究。

In vivo biodistribution and toxicology of carboxylated graphene quantum dots.

机构信息

Department of Polymer Science and Engineering, Korea National University of Transportation, Chungbuk 380-702, Republic of Korea.

出版信息

ACS Nano. 2013 Aug 27;7(8):6858-67. doi: 10.1021/nn402043c. Epub 2013 Jul 9.

Abstract

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.

摘要

具有迷人的光学和电子特性的发磷光的石墨烯量子点(GQDs)在生物医学工程中有许多有前途的应用。在这项工作中,我们首先研究了羧基化发磷光的 GQDs 的体内分布和潜在毒性。KB、MDA-MB231、A549 癌细胞和 MDCK 正常细胞系被选为体外细胞培养模型,以检查羧基化发磷光 GQDs 的可能不良影响。羧基化 GQDs 具有增加的水溶性。所有癌细胞都有效地摄取了羧基化 GQDs。在所测试的暴露水平下,在这两个系统中均未观察到急性毒性或形态变化。长期的体内研究表明,GQDs 在静脉注射后主要在肝脏、脾脏、肺、肾脏和肿瘤部位积累。为了揭示 GQDs 对治疗小鼠的任何潜在毒性作用,进行了血清生化分析和组织学评估。血清生化和全血细胞计数研究的毒性结果表明,GQDs 对治疗动物没有明显的毒性。最后,在 5mg/kg 或 10mg/kg 剂量下给药 21 天后,我们观察到 GQDs 处理的小鼠没有明显的器官损伤或病变。通过充分的体外和体内毒性研究,发磷光的 GQDs 可用于生物应用。

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