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Herein, we demonstrate the potential of ultrabright fluorescent silica-coated organic nanocrystals for two-photon in vivo imaging. These unique nanoparticles (NPs) containing a crystalline core of small push–pull dipolar dye are specifically designed to exhibit two-photon absorption for fluorescence imaging. The NPs can be easily functionalized using click chemistry in pure water, with preservation of the organic core. A novel small-volume DLS technique was used to evaluate the effect of PEGylation on the colloidal stability of the NPs in complex media containing salts and proteins, mimicking the composition of blood serum. The potential of these bright red-emitting NPs for two-photon fluorescence imaging is demonstrated both in vitro and in vivo. [ABSTRACT FROM AUTHOR]

A novel and efficient method for ligand exchange on core-shell nanocrystals is described. Carbon disulfide reacts with amine-containing ligand during the process and the resulting dithiocarbamates are strongly bound to the surface of quantum dots giving a secure coating of the nanoparticle.

A polymerizable amphiphile polymer containing PEG was synthesized and used to encapsulate quantum dots in micelles. The quantum dot micelles were then polymerized using a "clean" electron beam process that did not require any post-irradiation purification. Fluorescence spectroscopy revealed that the polymerized micelles provided an organic coating that preserved the quantum dot fluorescence better than nonpolymerized micelles, even under harsh conditions., (© 2011 American Chemical Society)

Water soluble fluorescent nanocrystals were obtained by encapsulation of hydrophobic quantum dots (QDs) with amphiphilic phospholipids derived from the ring opening metathesis of norbornene-based monomers. The robustness of the newly coated quantum dots was assessed by comparative studies under various ionic conditions which indicated an overall enhancement of their fluorescence stability.