The synthesis using the thermal decomposition of metal trifluoroacetates is being widely used to prepare oleatecapped lanthanide-doped upconverting NaYF 4 :Er 3þ /Yb 3þ nanoparticles (Ln-UCNPs). These nanoparticles have no inherent aqueous dispersibility and inconvenient postsynthesis treatments are required to render them water dispersible. Here, we have developed a novel and facile approach to obtain water-dispersible, ligand-free, brightly upconverting Ln-UCNPs. We show that the upconversion luminescence is affected by the local environment of the lanthanide ions at the surface of the Ln-UCNPs. We observe a dramatic difference of the integrated upconverted red:green emission ratio for Ln-UCNPs dispersed in toluene compared to Ln-UCNPs dispersed in water. We can enhance or deactivate the upconversion luminescence by pH and H/D isotope vibronic control over the competitive radiative and nonradiative relaxation pathways for the red and green excited states. Direct biofunctionalization of the ligand-free, water-dispersible Ln-UCNPs will enable myriad new opportunities in targeting and drug delivery applications.

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A new approach to deep tissue imaging is presented based on 8 nm CdTe semiconductor quantum dots (QDs). The characteristic 800 nm emission was found to be efficiently excited via two-photon absorption of 900 nm photons. The fact that both excitation and emission wavelengths lie within the "biological window" allows for high resolution fluorescence imaging at depths close to 2 mm. These penetration depths have been used to obtain the first deep tissue multiphoton excited fluorescence image based on CdTe-QDs. Due to the large thermal sensitivity of CdTe-QDs, one may envisage, in the near future, their use in high resolution deep-tissue thermal imaging.

We report on the functionalization of ligand-free NaGdF(4):Er(3+), Yb(3+) upconverting nanoparticles with heparin and basic fibroblast growth factor (bFGF). These upconverting nanoparticles are used to obtain high-contrast images of HeLa cells. These images reveal that the heparin-bFGF functionalized nanoparticles show specific binding to the cell membrane.

With the rise of nanotechnologies, the risk of contamination of aquatic ecosystems with nanoparticles is increasing. Glycodendrimer-coated gold nanoparticles have been developed for biomedical applications; however, their effect on microalgae has never been studied. In this report, their interactions with algae were investigated using two strains of Chlamydomonas reinhardtii, a wild type having cell wall and a cell wall-deficient mutant. Cultures were exposed 48 h to 6 and 12 ng ml⁻¹ of gold nanoparticles coated with mannose generation 0 polyamidoamine dendrimer. Culture aggregation was found only for wild type cells, probably because of interactions between mannose and cell wall glycoproteins. Nanoparticles penetrated cytoplasm in both strains; however, inhibition of algal growth and photosynthetic activity was found only in the wild type. We conclude that nanoparticles' deteriorating effect in algae is caused by interactions with the cell wall, causing an aggregation of cell culture, and not by nanoparticle penetration inside the cytoplasm.