Gold nanoclusters are emerging as new materials for biomedical applications because of promises offered by their ultrasmall size and excellent biocompatibility. Here, the synthesis and optical and biological characterizations of a highly luminescent folate-functionalized Au22 cluster (Au22-FA) are reported. The Au22-FA clusters are synthesized by functionalizing the surface of Au22(SG)18 clusters, where SG is glutathione, with benzyl chloroformate and folate. The functionalized clusters are highly water-soluble and exhibit remarkably bright luminescence with a quantum yield of 42%, significantly higher than any other water-soluble gold clusters protected with thiolate ligands. The folate groups conjugated to the gold cluster give rise to additional luminescence enhancement by energy transfer sensitization. The brightness of Au22-FA is found to be 4.77 mM−1 cm−1, nearly 8-fold brighter than that of Au22(SG)18. Further biological characterizations have revealed that the Au22-FA clusters are well-suited for bioimaging. The Au22-FA clusters exhibit excellent photostability and low toxicity; nearly 80% cell viability at 1000 ppm of the cluster. Additionally, the Au22-FA clusters show target specificity to folate-receptor positive cells. Finally, the time-course in vivo luminescence images of intravenous-injected mice show that the Au22-FA clusters are renal-clearable, leaving only 8% of them remained in the body after 24 h post-injection.
Folate-functionalized Au22 nanoclusters show the highest luminescence quantum yield of 42% among other water-soluble gold nanoclusters protected with thiolate ligands. The brightness is enhanced by 8-fold via the rigidification of the surface shell and energy transfer sensitization from the photoexcited folate. The highly luminescent gold clusters with excellent biocompatibility and active targeting ability are well-suited to targeted bioimaging.
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