Synthesis and bioactivity of the folate receptor targeted gamma-cyclodextrin-folate inclusion-coated CdSe/ZnS quantum dots / 药学学报
Acta Pharmaceutica Sinica
; (12): 566-572, 2013.
Article
em Zh
| WPRIM
| ID: wpr-235626
Biblioteca responsável:
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.
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Espectrofotometria Ultravioleta
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Sulfetos
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Células HeLa
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Espectroscopia de Ressonância Magnética
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Sobrevivência Celular
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Química
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Compostos de Zinco
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Espectroscopia de Infravermelho com Transformada de Fourier
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Compostos de Selênio
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Compostos de Cádmio
Limite:
Humans
Idioma:
Zh
Revista:
Acta Pharmaceutica Sinica
Ano de publicação:
2013
Tipo de documento:
Article