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One-pot aqueous synthesis of highly strained CdTe/CdS/ZnS nanocrystals and their interactions with cells
Author(s) -
Mehriban Ulusoy,
JohannaGabriela Walter,
Antonina Lavrentieva,
Imme Kretschmer,
Lydia Sandiford,
Alix Le Marois,
Rebecca Bongartz,
Pooyan Aliuos,
Klaus Suhling,
Frank Stahl,
Mark Green,
Thomas Scheper
Publication year - 2014
Publication title -
rsc advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.746
H-Index - 148
ISSN - 2046-2069
DOI - 10.1039/c4ra13386b
Subject(s) - nanocrystal , cadmium telluride photovoltaics , aqueous solution , materials science , shell (structure) , nanotechnology , deposition (geology) , conjugated system , aptamer , nanoparticle , core (optical fiber) , quantum dot , chemical engineering , chemistry , polymer , composite material , genetics , engineering , biology , paleontology , sediment
In this work, a very simple one-pot synthetic approach was developed to generate aqueous CdTe/CdS/ZnS type-II/type-I red-emitting nanocrystals (NCs). Strain-induced optical properties of CdTe/CdS particles having core((small))/shell((thick)) structure with a maximum quantum yield (QY(max)) similar to 57% were further improved with the overgrowth of a ZnS shell, resulting in a core((small))/shell((thick))/shell((small)) structure (QY(max) similar to 64%). The spectral properties were tuned further to the near-infrared region as the ZnS shell grew in thickness. X-ray powder diffraction (XRD) analysis and high-resolution transmission electron microscope (HRTEM) images showed the crystalline structure of NCs proving the epitaxial growth of ZnS without crystalline defects. Under continuous UV-irradiation for 5 h, the NCs did not exhibit any photo-degradation but instead displayed a photo-annealing process. These extremely photostable NCs were further characterized in terms of their cytotoxicity and their cell labeling performances. The presence of a ZnS shell was found to reduce the toxicity of the CdTe/CdS NCs. Furthermore, aptamer-conjugated NCs were successfully utilized in targeted cell imaging. Promisingly, the aptamer-NCs bioconjugates were internalized by A549 cells within 2 hours of incubation and retained their fluorescence even after 24 hours of internalization.DAA

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