Carbon Quantum Dots: In vitro and in vivo Studies on Biocompatibility and Biointeractions for Optical Imaging

Int J Nanomedicine. 2020 Aug 28:15:6519-6529. doi: 10.2147/IJN.S257645. eCollection 2020.

Abstract

Background: Understanding the biocompatibility and biointeractions of nano-carbon quantum dots (nano-CQDs) in vitro and in vivo is important for assessing their potential risk to human health. In the previous research, the physical properties of CQDs synthesized by the laser ablation in liquid (LAL) method were analyzed in detail; however, possible bioapplications were not considered.

Materials and methods: CQDs were prepared by LAL and characterized by atomic force microscopy, fluorescence lifetime, absorption spectrum, Fourier-transform infrared spectroscopy, and dynamic light scattering. Their biocompatibility was evaluated in vitro using assays for cytotoxicity, apoptosis, and biodistribution and in vivo using immunotoxicity and the relative expression of genes. Cells were measured in vitro using fluorescence-lifetime imaging microscopy to analyze the biointeractions between CQDs and intracellular proteins.

Results: There were no significant differences in biocompatibility between the CQDs and the negative control. The intracellular interactions had no impact on the optical imaging of CQDs upon intake by cells. Optical imaging of zebrafish showed the green fluorescence was well dispersed.

Conclusion: We have demonstrated that the CQDs have an excellent biocompatibility and can be used as efficient optical nanoprobes for cell tracking and biomedical labeling except for L929 and PC-3M cells.

Keywords: biodistribution; biointeraction; immunotoxicity; nanoprobe; optical imaging.

MeSH terms

  • Animals
  • Antigens, CD / blood
  • Apoptosis / drug effects
  • Carbon / chemistry
  • Dynamic Light Scattering
  • Gene Expression Regulation / drug effects
  • Hep G2 Cells
  • Humans
  • Liver / drug effects
  • Liver / physiology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Electron, Scanning
  • Microscopy, Electron, Transmission
  • Microscopy, Fluorescence
  • Optical Imaging
  • Quantum Dots / chemistry*
  • Quantum Dots / toxicity*
  • RAW 264.7 Cells
  • Reactive Oxygen Species / metabolism
  • Spectroscopy, Fourier Transform Infrared
  • Tissue Distribution
  • Toxicity Tests
  • Zebrafish

Substances

  • Antigens, CD
  • Reactive Oxygen Species
  • Carbon

Grants and funding

This work was funded by the National Nature Science Foundation of China (grants 81771891 and 81470724), the Natural Science Foundation of Guangdong Province (grant Q195026028), the Science and Technology Project of Guangdong Province (grant 2017B090911012), and the University Innovation and Entrepreneurship Education Major Project of Guangzhou City (item 201709P05).