Abstract

Lanthanide-doped upconversion nanoparticles (UCNPs) have attracted considerable attentions in the area of molecular imaging, targeted therapy and diagnosis. The UCNPs synthesized by conventional methods are usually hydrophobic and require additional surface modification to give them water solubility and biocompatibility. Herein, we designed a simple and convenient strategy for the direct synthesis of water-soluble and biocompatible lanthanum-doped UCNPs through a one-pot reaction without further purification and screening. The doping amount of lanthanide can be adjusted by simply changing the proportion of precursor in the reaction solution. The resulting water-soluble UCNPs possess excellent colloidal stability in physiological media. Under 980 nm excitation, NaGdF4:Yb3+/Er3+ and NaGdF4:Yb3+/Tm3+ nanoparticles exhibited a dominant green emission band (4S3/2→4I15/2) of Er3+ and a dominant blue emission band (1G4→3H6) of Tm3+, respectively. Toxic response was not observed with concentration up to 50 mg/L. The hemolysis to rabbit red blood cells was less than 2% in the concentration up to 20 mg/L. The NaGdF4:Yb3+/Er3+ nanoparticles exhibited a high r1 relaxivity of 4.7 mM−1s−1, demonstrating that the water-soluble and biocompatible UCNPs can be efficient T1 contrast agents. The in vivo results show that UCNPs exhibit excellent T1-weighted imaging and fluorescence imaging abilities simultaneously, and can be used as a versatile promising theranostic nanoplatform.

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