X-ray excited luminescence spectroscopy and imaging with NaGdF 4 :Eu and Tb.
Meenakshi RanasingheMd ArifuzzamanApeksha C RajamanthrilageW R WilloughbyAshley DickeyColin McMillenJoseph W KolisMark BoldingJeffrey N AnkerPublished in: RSC advances (2021)
X-ray excited optical luminescence from nanophosphors can be used to selectively generate light in tissue for imaging and stimulating light-responsive materials and cells. Herein, we synthesized X-ray scintillating NaGdF 4 :Eu and Tb nanophosphors via co-precipitate and hydrothermal methods, encapsulated with silica, functionalized with biotin, and characterized by X-ray excited optical luminescence spectroscopy and imaging. The nanophosphors synthesized by co-precipitate method were ∼90 and ∼106 nm in diameter, respectively, with hydrothermally synthesized particles showing the highest luminescence intensity. More importantly, we investigated the effect of thermal annealing/calcination on the X-ray excited luminescence spectra and intensity. At above 1000 °C, the luminescence intensity increased, but particles fused together. Coating with a 15 nm thick silica shell prevented particle fusion and enabled silane-based chemical functionalization, although luminescence decreased largely due to the increased mass of non-luminescent material. We observed an increase in luminesce intensity with temperature until at 400 °C. At above 600 °C, NaGdF 4 :Eu@SiO 2 converts to NaGd 9 Si 6 O 26 :Eu, an X-ray scintillator brighter than annealed NPs at 400 °C and dimmer than NPs synthesized using the hydrothermal method. The particles generate light through tissue and can be selectively excited using a focused X-ray source for imaging and light generation applications. The particles also act as MRI contrast agents for multi-modal localization.
Keyphrases
- high resolution
- energy transfer
- quantum dots
- light emitting
- dual energy
- mass spectrometry
- high intensity
- high speed
- tandem mass spectrometry
- sensitive detection
- oxide nanoparticles
- contrast enhanced
- atomic force microscopy
- signaling pathway
- drug delivery
- single molecule
- pi k akt
- optical coherence tomography
- liquid chromatography
- solid state