4.8 Article

Molecular imaging of biological systems with a clickable dye in the broad 800-to 1,700-nm near-infrared window

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1617990114

Keywords

NIR-II molecular imaging; bioconjugate; clickable dye; density gradient ultracentrifugation separation; NIR-II multicolor molecular imaging

Funding

  1. Calbrain Program
  2. National Institutes of Health [R01 HL127113-01A1]
  3. South University of Science and Technology of China
  4. Recruitment Program of Global Youth Experts of China, Shenzhen Key Lab Funding Grant [ZDSYS201505291525382]
  5. Shenzhen Peacock Program Grant [KQTD20140630160825828]
  6. International Postdoctoral Exchange Fellowship Program - Office of China Postdoctoral Council [20150031]
  7. Jilin/Stanford University

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Fluorescence imaging multiplicity of biological systems is an area of intense focus, currently limited to fluorescence channels in the visible and first near-infrared (NIR-I; similar to 700-900 nm) spectral regions. The development of conjugatable fluorophores with longer wavelength emission is highly desired to afford more targeting channels, reduce background autofluorescence, and achieve deeper tissue imaging depths. We have developed NIR-II (1,000-1,700 nm) molecular imaging agents with a bright NIR-II fluorophore through high-efficiency click chemistry to specific molecular antibodies. Relying on buoyant density differences during density gradient ultracentrifugation separations, highly pure NIR-II fluorophore-antibody conjugates emitting similar to 1,100 nm were obtained for use as molecular-specific NIR-II probes. This facilitated 3D staining of similar to 170-mu m histological brain tissues sections on a home-built confocal microscope, demonstrating multicolor molecular imaging across both the NIR-I and NIR-II windows (800-1,700 nm).

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