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ABSTRACT: Water-dispersible amphiphilic surface-engineered quantum dots (QDs) were found to be strongly accumulated within discrete zones of the exopolymer network of Shewanella oneidensis MR-1 biofilms, but not to the cell surfaces. These microdomains showed a patterned distribution in the exopolymer matrix, and led to a restricted diffusion of the amphiphilic nanoparticles.
Applied and environmental microbiology 12/2012; · 3.69 Impact Factor
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ABSTRACT: Quantum dots (QDs) nanoprobes are emerging as alternatives to small-molecule fluorescent probes in biomedical technology. This paper reports an efficient and rapid method of producing highly dispersed and stable CdSe-core QDs with a hydrophobic gradient. Amphiphilic core/shell CdSe/ZnS QDs were prepared by ligand exchange at the surface of lipophilic CdSe/ZnS QDs using the dihydrolipoic acid (DHLA) dithiol ligand linked to leucine or phenylalanine amino acids. Contact angle relaxations on a hydrophobic surface and surface tension measurements indicated that aqueous dispersions of CdSe/ZnS@DHLA-Leu or CdSe/ZnS@DHLA-Phe QDs exhibit increased hydrophobicity compared to CdSe-core QDs capped by the hydrophilic 3-mercaptopropionic acid (MPA) ligand. We found that the surface functional groups and the ligand density at the periphery of these QDs significantly dictated their interactions with a complex biological matrix called biofilm. Using fluorescence confocal microscopy and an autocorrelation function (semi-variogram), we demonstrated that MPA-capped QDs were homogeneously associated to the biopolymers, while amphiphilic CdSe/ZnS@DHLA-Leu or CdSe/ZnS@DHLA-Phe QDs were specifically confined allowing identification of hydrophobic microdomains of the biofilms. Results obtained clearly point out that the final destination of QDs in biofilms can properly be controlled by an appropriate design of surface ligands.
Biomaterials 08/2011; 32(23):5459-70. · 7.40 Impact Factor
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Berichte der deutschen chemischen Gesellschaft 01/2011; 2011(6):794 - 801. · 2.94 Impact Factor
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ABSTRACT: New quantum dots (QDs) were fabricated with a core/shell/shell structure consisting of CdTe core/CdS shell/ZnO shell. Despite the high lattice mismatch between CdS and ZnO, a ZnO shell was successfully introduced by basic hydrolysis of Zn(OAc)2 at the surface of core/shell CdTe/CdS QDs stabilized by 3-mercaptopropionic acid (MPA). The core/shell/shell CdTe/CdS/ZnO@MPA QDs exhibited a significant redshift of emission peaks (up to 50 nm for green-emitting CdTe/CdS QDs) when the shell grew. By changing the size of the core or the thickness of the ZnO shell, the emission colors of the obtained nanocrystals can be tuned between the green and red regions of the spectrum following an identical procedure. The influence of ZnO shell growth on photoluminescence (PL) quantum yields was found to be more pronounced for CdTe/CdS samples with green or yellow emission for which quantum yields increased up to three times. The epitaxial growth of the ZnO shell was confirmed by X-ray photoelectron spectroscopy and luminescence decay experiments. Because of the passivation of surface defects, a PL lifetime of 33.6 ns was measured for core/shell/shell CdTe/CdS/ZnO QDs prepared with a Zn/Cd ratio of 0.8, while it was only 17.7 ns for core/shell CdTe/CdS QDs.
The Journal of Physical Chemistry C 11/2009; 113:19458-19467. · 4.80 Impact Factor
