王黎

个人信息Personal Information

副教授

硕士生导师

性别:女

毕业院校:兰州大学

学位:博士

所在单位:化工海洋与生命学院

联系方式:wang_li@dlut.edu.cn

电子邮箱:wang_li@dlut.edu.cn

扫描关注

论文成果

当前位置: 中文主页 >> 科学研究 >> 论文成果

PEGylated doxorubicin cloaked nano-graphene oxide for dual-responsive photochemical therapy

点击次数:

论文类型:期刊论文

发表时间:2019-02-25

发表刊物:INTERNATIONAL JOURNAL OF PHARMACEUTICS

收录刊物:SCIE、PubMed、Scopus

卷号:557

页面范围:66-73

ISSN号:0378-5173

关键字:Nano-graphene oxide; Photochemical therapy; pH sensitive; Nano-drug delivery system; Doxorubicin

摘要:Graphene oxide (GO) owns huge surface area and high drug loading capacity for aromatic molecules, such as doxorubicin (DOX). However, its biocompatibility is poor and it might agglomerate in physiological conditions. Chemical modification of GO with hydrophilic polymer, especially PEGylation, was a common method to improve its biocompatibility. But the chemical modification of GO was complicated, and its drug loading capacity might be reduced because of the occupation of its functional groups. In this study, DOX-PEG polymers with different PEG molecular weights were synthesized to modify nano graphene oxide (NGO) to simultaneously realize the solubilization of NGO and the high loading capacity of DOX. The result showed that the drug release of NGO@DOX-PEG was pH sensitive. NIR irradiation could augment the drug release, cellular uptake, cytotoxicity and nuclear translocation of nanodrugs. Among the three kinds of nanodrugs, NGO@DOX-PEG5K was superior to others. It suggested that after conjugating with PEG, the bond between DOX-PEG and NGO was weakened, which resulted in a better drug release and treatment effect. In summary, the NIR and pH dual-responsive NGO@DOX-PEG nanodrugs were developed by noncovalent modification, and it demonstrated excellent biocompatibility and photochemical therapeutic effect, presenting a promising candidate for antitumor therapy, especially NGO@DOX-PEG5K.