Abstract

Event Abstract Back to Event Blood compatibility evaluations of fluorescent carbon dots Sha Li1 1 Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, China In 2004, scientists in Clemson University of America created firstly a type of new carbon nanomaterial-fluorescent carbon dots. Compared with other fluorescent nanomaterials, fluorescent carbon dots have a variety of advantages such as a wide range of raw materials, simple preparation process, low biological toxicity, good biocompatibility and excitation wavelength-dependent photoluminescence, etc[1]. Therefore, fluorescent carbon dots have attracted more and more attention in many biomedical applications including biological probe, bio-imaging, cell labeling, biosensor, disease diagnosis, and drug delivery, etc[2]-[3]. In these biomedical applications, carbon dots will inevitably contact with blood tissue, so it is essential to evaluate in vitro and vivo blood compatibility of fluorescent carbon dots, which will promote the clinical application of fluorescent carbon dots. We prepared fluorescent carbon dots by hydrothermal carbonization of α-cyclodextrin. The fluorescent carbon dots had uniform particle size and strong blue fluorescence, such as Figure. 1. In this work, we investigated the effects of the fluorescent carbon dots on the structure and function of key blood components in vitro and the blood clotting in vivo. The results show that the effect of the fluorescence carbon dots on blood components with concentration dependent. It only had a weak effect on blood components with the fluorescence carbon dots ≤0.1 mg/mL. However, higher concentrations of the fluorescence carbon dots impaired the normal structures and functions of the key blood components in vitro. No blood coagulation and organs damage were found, when the dose of the fluorescence carbon dots ≤50 mg/kg. These findings provide important information for circumventing the potential risks and promoting the clinical applications of the fluorescent carbon dots.

Highlights

  • Blood Compatibility Evaluations of Fluorescent Carbon Dots

  • 2.1 Quantitative analysis for the cellular uptake of the carbon dots Hela cells were seeded in a 24-well plate (1×105 cells/well), and cultured with DMEM medium overnight

  • The cells were incubated with 0.1, 0.5 or 1 mg/mL of the carbon dots dissolved in DMEM medium

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Summary

Introduction

Blood Compatibility Evaluations of Fluorescent Carbon Dots * Corresponding authors: Zonghua Liu E-mail: tliuzonghua@jnu.edu.cn Tel and Fax: 86-20-85226397 1.1 Quantitative analysis for the cellular uptake of the carbon dots 1.2 Morphology of the carbon dots-treated RBCs in the presence of BSA

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