Objective To evaluate the bio-safety of graphene quantum dots （GQDs）, we studied its effects on the embryonic development of zebrafish. Methods In vivo, biodistribution and the developmental toxicity of GQDs were in...Objective To evaluate the bio-safety of graphene quantum dots （GQDs）, we studied its effects on the embryonic development of zebrafish. Methods In vivo, biodistribution and the developmental toxicity of GQDs were investigated in embryonic zebrafish at exposure concentrations ranging from 12.5-200μg/mL for 4-96 h post-fertilization （hpf）. The mortality, hatch rate, malformation, heart rate, GQDs uptake, spontaneous movement, and larval behavior were examined. Results The fluorescence of GQDs was mainly localized in the intestines and heart. As the exposure concentration increased, the hatch and heart rate decreased, accompanied by an increase in mortality. Exposure to a high level of GQDs （200μg/mL） resulted in various embryonic malformations including pericardial edema, vitelline cyst, bent spine, and bent tail. The spontaneous movement significantly decreased after exposure to GQDs at concentrations of 50, 100, and 200μg/mL. The larval behavior testing （visible light test） showed that the total swimming distance and speed decreased dose-dependently. Embryos exposed to 12.5 μg/mL showed hyperactivity while exposure to higher concentrations （25, 50, 100, and 200μg/mL） caused remarkable hypoactivity in the light-dark test. Conclusion Low concentrations of GODs were relatively non-toxic. However, GQDs disrupt the progression of embryonic development at concentrations exceeding 50 μg/mL.展开更多
基金supported by grants from the Key Program of the National Natural Science Foundation of China(U1432248)the National Natural Science Foundation of China(11305226,11175222)
文摘Objective To evaluate the bio-safety of graphene quantum dots （GQDs）, we studied its effects on the embryonic development of zebrafish. Methods In vivo, biodistribution and the developmental toxicity of GQDs were investigated in embryonic zebrafish at exposure concentrations ranging from 12.5-200μg/mL for 4-96 h post-fertilization （hpf）. The mortality, hatch rate, malformation, heart rate, GQDs uptake, spontaneous movement, and larval behavior were examined. Results The fluorescence of GQDs was mainly localized in the intestines and heart. As the exposure concentration increased, the hatch and heart rate decreased, accompanied by an increase in mortality. Exposure to a high level of GQDs （200μg/mL） resulted in various embryonic malformations including pericardial edema, vitelline cyst, bent spine, and bent tail. The spontaneous movement significantly decreased after exposure to GQDs at concentrations of 50, 100, and 200μg/mL. The larval behavior testing （visible light test） showed that the total swimming distance and speed decreased dose-dependently. Embryos exposed to 12.5 μg/mL showed hyperactivity while exposure to higher concentrations （25, 50, 100, and 200μg/mL） caused remarkable hypoactivity in the light-dark test. Conclusion Low concentrations of GODs were relatively non-toxic. However, GQDs disrupt the progression of embryonic development at concentrations exceeding 50 μg/mL.
