TY - JOUR
T1 - Phototoxicity Generated by Silicon Quantum Dot Nanoparticles on Zebrafish Embryos
AU - Srivastava, Prateek K.
AU - Han, Shanshan
AU - Tu, Chang Ching
AU - Jing, Lili
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/6/3
Y1 - 2019/6/3
N2 - We demonstrate phototoxicity generated by silicon quantum dot nanoparticles (SiQDNPs) using zebrafish as an animal model. Having long exciton lifetime, the SiQDNPs can function as photosensitizers which absorb incident optical light and transfer the energy to oxygen molecules in close proximity, generating cytotoxic singlet oxygens. First, the zebrafish embryos were soaked in the SiQDNP suspension in E3 medium, while being illuminated under blue light or kept in the dark for 6 h. Through neutral red staining immediately afterward, the illuminated embryos showed more prominent injuries at their head, yolk sac and tail parts than those in the dark. Furthermore, prolonged observation after the treatment revealed that the illuminated embryos had mortality rates significantly higher than those without illumination, clearly showing the phototoxicity effect generated by the SiQDNPs. However, adverse effect due to the immersion of whole embryos in the SiQDNP suspension was also observed. To alleviate this issue, minute amounts of the SiQDNPs were microinjected to the embryos, followed by blue light illumination. By acridine orange staining subsequently, cell apoptosis localized near the microinjection site was revealed, whereas no apoptosis was found for those also microinjected with the SiQDNPs but without illumination. The phototoxicity effect demonstrated on zebrafish embryos in this work manifests the potential of using the SiQDNPs as a photosensitizer for photodynamic therapy.
AB - We demonstrate phototoxicity generated by silicon quantum dot nanoparticles (SiQDNPs) using zebrafish as an animal model. Having long exciton lifetime, the SiQDNPs can function as photosensitizers which absorb incident optical light and transfer the energy to oxygen molecules in close proximity, generating cytotoxic singlet oxygens. First, the zebrafish embryos were soaked in the SiQDNP suspension in E3 medium, while being illuminated under blue light or kept in the dark for 6 h. Through neutral red staining immediately afterward, the illuminated embryos showed more prominent injuries at their head, yolk sac and tail parts than those in the dark. Furthermore, prolonged observation after the treatment revealed that the illuminated embryos had mortality rates significantly higher than those without illumination, clearly showing the phototoxicity effect generated by the SiQDNPs. However, adverse effect due to the immersion of whole embryos in the SiQDNP suspension was also observed. To alleviate this issue, minute amounts of the SiQDNPs were microinjected to the embryos, followed by blue light illumination. By acridine orange staining subsequently, cell apoptosis localized near the microinjection site was revealed, whereas no apoptosis was found for those also microinjected with the SiQDNPs but without illumination. The phototoxicity effect demonstrated on zebrafish embryos in this work manifests the potential of using the SiQDNPs as a photosensitizer for photodynamic therapy.
KW - photodynamic therapy
KW - phototoxicity
KW - silicon quantum dot
KW - singlet oxygen
KW - zebrafish embryo
UR - http://www.scopus.com/inward/record.url?scp=85070543582&partnerID=8YFLogxK
U2 - 10.1021/acsabm.9b00264
DO - 10.1021/acsabm.9b00264
M3 - 期刊論文
C2 - 35030821
AN - SCOPUS:85070543582
SN - 2576-6422
VL - 2
SP - 2872
EP - 2878
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 7
ER -