4.8 Article

Aggregation-Induced Emission Luminogen-Embedded Silica Nanoparticles Containing DNA Aptamers for Targeted Cell Imaging

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 1, Pages 609-616

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b09644

Keywords

aggregation-induced emission; silica nanoparticle; DNA aptamer; photoactivatable fluorescence; cell imaging

Funding

  1. National Natural Science Foundation of China [2142200199, 21390410, 21375074]
  2. National Key Scientific Instrument and Equipment Development Project of China [2012YQ030111]
  3. Tsinghua University Initiative Scientific Research Program [20131089220]
  4. Recruitment Program of Global Youth Experts of China

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Conventional fluorophores usually undergo aggregation-caused quenching (ACQ), which limits the loading amount of these fluorophores in nanoparticles for bright fluorescence imaging. On the contrary, fluorophores with aggregation-induced emission (AIE) characteristics are strongly fluorescent in their aggregate states and have been an ideal platform for developing highly fluorescent nanomaterials, such as fluorescent silica nanoparticles (FSNPs). In this work, AIE luminogens based on salicylaldehyde hydrazones were embedded in silica nanoparticles through a facile noncovalent approach, which afforded AIE-FSNPs emitting much brighter fluorescence than that of some commercial fluorescein-doped silica and polystyrene nanoparticles. These AIE-FSNPs displaying multiple fluorescence colors were fabricated by a general method, and they underwent much less fluorescence variation due to environmental pH changes compared with fluorescein-hybridized FSNPs. In addition, a DNA aptamer specific to nucleolin was functionalized on the surface of AIE-FSNPs for targeted cell imaging. Fluorescent microscopy and flow cytometry studies both revealed highly selective fluorescence staining of MCF-7 (a cancer cell line with nucleolin overexpression) over MCF-10A (normal) cells by the aptamer-functionalized AIE-FSNPs. The fluorescence imaging in different color channels was achieved using AIE-FSNPs containing each of the AIE luminogens, as well as photoactivatable fluorescent imaging of target cells by the caged AIE fluorophore.

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