4.8 Article

Autofluorescence-Free Immunoassay Using X-ray Scintillating Nanotags

Journal

ANALYTICAL CHEMISTRY
Volume 90, Issue 11, Pages 6992-6997

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.8b01315

Keywords

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Funding

  1. National Natural Science Foundation of China [21635002, U1505221, 21505021, 21622502]
  2. Natural Science Foundation of Fujian Province of China [2015H6011, 2016J05035, 2017J06004]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT15R11]
  4. outstanding youth scientific research personnel training plan of colleges and universities in Fujian Province
  5. Health-Education joint research project of Fujian Province [WKJ2016-2-23]

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Autofluorescence background in complex biological samples is a major challenge in achieving high sensitivity of fluorescence immunoassays (FIA). Here we report an X-ray luminescence-based immunoassay for high-sensitivity detection of biomarkers using X-ray scintillating nanotags. Due to the weak scattering and absorption of most biological chromophores by X-ray excitation, a low-dose X-ray source can be used to produce intense scintillating luminescence from the nanotags for autofluorescence-free biosensing. To demonstrate this concept, we designed and synthesized NaGdF4:Tb@NaYF4 core/shell nanopartides as kind of high-efficiency X-ray scintillating nanotags, which are able to convert high-energy X-ray photons to visible light without autofluorescence in biological samples. Notably, strong X-ray absorption and minimized surface quenching arising from the heavy Gd3+/Tb3+ atoms and core/shell architecture of the nanopartides were found to be critically important for high efficiency X-ray excited luminescence for high-sensitivity biosensing. Our method allows for sensing alpha-fetoprotein (AFP) biomarkers with a detection limit down to 0.25 ng/mL. Moreover, the as-described X-ray luminescence immunoassay exhibited an excellent biological specificity, high stability, and sample recovery, implying an opportunity for applications in complex biological samples. Consequently, our method can be readily extended for multiplexing sensing and medical diagnosis.

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