4.8 Article

Stable, Bright, and Long-Fluorescence-Lifetime Dyes for Deep-Near-Infrared Bioimaging

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 31, Pages 14351-14362

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c05826

Keywords

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Funding

  1. National Natural Science Foundation of China [21822805, 21908065, 12034008, 91850202, 21873030, 11674101, 81922070, 22078098]
  2. China Postdoctoral Science Foundation [2019M651427, 2020T130197]
  3. Shanghai Rising-Star Program [21QA1402600]
  4. Research Fund of Happiness Flower ECNU [2020JK2103]
  5. Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism (Shanghai Municipal Education Commission)

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Near-infrared (NIR) fluorophores are important for biomedical applications, especially in the deep-NIR spectral region. This study successfully synthesized four silicon-substituted bis-benzannulated rhodamine dyes with high absorption, long fluorescence lifetime, and excellent stability. These dyes have great potential for bioimaging in the deep-NIR spectral region.
Near-infrared (NIR) fluorophores absorbing maximally in the region beyond 800 nm, i.e., deep-NIR spectral region, are actively sought for biomedical applications. Ideal dyes are bright, nontoxic, photostable, biocompatible, and easily derivatized to introduce functionalities (e.g., for bioconjugation or aqueous solubility). The rational design of such fluorophores remains a major challenge. Silicon-substituted rhodamines have been successful for bioimaging applications in the red spectral region. The longer-wavelength silicon-substituted congeners for the deep-NIR spectral region are unknown to date. We successfully prepared four silicon-substituted bis-benzannulated rhodamine dyes (ESi5a-ESi5d), with an efficient five-step cascade on a gram-scale. Because of the extensive overlapping of their HOMO-LUMO orbitals, ESi5a-ESi5d are highly absorbing (lambda(abs) approximate to 865 nm and epsilon > 10(5) cm(-1) M-1). By restraining both the rotational freedom via annulation and the vibrational freedom via silicon-imparted strain, the fluorochromic scaffold of ESi5 is highly rigid, resulting in an unusually long fluorescence lifetime (tau > 700 ps in CH2Cl2) and a high fluorescence quantum yield (phi = 0.14 in CH2Cl2). Their half-lives toward photobleaching are 2 orders of magnitude longer than the current standard (ICG in serum). They are stable in the presence of biorelevant concentration of nucleophiles or reactive oxygen species. They are minimally toxic and readily metabolized. Upon tail vein injection of ESi5a (as an example), the vasculature of a nude mouse was imaged with a high signal-to-background ratio. ESi5 dyes have broad potentials for bioimaging in the deep-NIR spectral region.

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