Fabrication of Graphitic Carbon Nitride Quantum Dots and Their Application for Simultaneous Fluorescence Imaging and pH-Responsive Drug Release

被引:37
作者
Dong, Jian [1 ]
Zhao, Yanli [1 ]
Wang, Kaiqi [1 ]
Chen, Hongyu [1 ]
Liu, Li [1 ]
Sun, Baoliang [2 ,3 ]
Yang, Mingfeng [2 ,3 ]
Sun, Liping [1 ]
Wang, Yi [4 ,5 ]
Yu, Xuegang [6 ]
Dong, Lifeng [1 ]
机构
[1] Taishan Med Univ, Sch Chem & Pharmaceut Engn, Tai An 271016, Shandong, Peoples R China
[2] Univ Shandong, Key Lab Cerebral Microcirculat, Tai An 271016, Shandong, Peoples R China
[3] Taishan Med Univ, Affiliated Hosp, Dept Neurol, Tai An 271016, Shandong, Peoples R China
[4] Taishan Med Univ, Inst Optometry, Affiliated Hosp, Tai An 271016, Shandong, Peoples R China
[5] Taishan Med Univ, Dept Ophthalmol, Affiliated Hosp, Tai An 271016, Shandong, Peoples R China
[6] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
drug delivery; fluorescence imaging; graphitic carbon nitride; pH-responsive; quantum dots; PHASE C3N4 NANOSHEETS; NANO-GRAPHENE OXIDE; SELECTIVE DETECTION; LOADING EFFICIENCY; IN-VITRO; DELIVERY; SYSTEM; CHEMO; NANOCARRIERS; DOXORUBICIN;
D O I
10.1002/slct.201802492
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A simple approach is developed to produce fluorescent graphitic carbon nitride quantum dots (g-CNQDs) by refluxing bulk graphitic carbon nitride (g-C3N4) in HNO3 followed by a direct hydrothermal treatment. Owing to their small size, intrinsic optical properties, low toxicity, and useful non-covalent interactions with the antitumor drug doxorubicin (DOX), g-CNQDs are investigated as fluorescent nanocarriers for DOX without any pre-modification. The inherent fluorescence of g-CNQDs and DOX provides the drug delivery system (g-CNQDs-DOX) with dual-color imaging for revealing the intracellular localization of g-CNQDs and DOX release. The release profiles of DOX from g-CNQDs-DOX reveal a strong dependence on the environmental pH value, which is beneficial for mollifying side effects following chemotherapy. Cellular uptake of g-CNQDs-DOX indicates that not only DOX but also some g-CNQDs penetrate cell nuclei after 16 h of incubation, which leads g-CNQDs-DOX to be more toxic than DOX. The results demonstrate the feasibility of using g-CNQDs as a traceable and pH-responsive drug delivery system due to their unique structural properties.
引用
收藏
页码:12696 / 12703
页数:8
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