Synthesis and bioactivity of the folate receptor targeted gamma-cyclodextrin-folate inclusion-coated CdSe/ZnS quantum dots / 药学学报
Yao Xue Xue Bao
; (12): 566-572, 2013.
Article
in Zh
| WPRIM
| ID: wpr-235626
Responsible library:
WPRO
ABSTRACT
The gamma-cyclodextrin-folate (gamma-CD/FA) inclusion-coated CdSe/ZnS quantum dots (QDs) with folate-receptor (FR) targeted were synthesized by simple and convenient sonochemical method. The products were studied using Fourier transform infrared (FTIR), proton nuclear magnetic resonance (1H NMR), utraviolet-visible spectrometry (UV-vis), fluorescence spectrum and transmission electron micrographs (TEM). The results showed that the gamma-CD/FA-coated CdSe/ZnS QDs not only have good monodispersity and smaller size, but also have good optical performance, such as higher quantum yield (QY) and a long fluorescence lifetime. The cytotoxicity experiments showed that the gamma-CD/FA-coated CdSe/ZnS QDs have lower cytotoxicity and could more effectively enter cancer cells with FR over-expression. The QDs with 4-5 nm in diameter were relatively easy to enter the cell and to be removed through kidneys, so it is more suitable for biomedical applications for bioprobes and bioimaging.
Full text:
1
Index:
WPRIM
Main subject:
Spectrophotometry, Ultraviolet
/
Sulfides
/
HeLa Cells
/
Magnetic Resonance Spectroscopy
/
Cell Survival
/
Chemistry
/
Zinc Compounds
/
Spectroscopy, Fourier Transform Infrared
/
Selenium Compounds
/
Cadmium Compounds
Limits:
Humans
Language:
Zh
Journal:
Yao Xue Xue Bao
Year:
2013
Type:
Article