Sterically Shielded Heptamethine Cyanine Dyes for Bioconjugation and High Performance Near‐Infrared Fluorescence Imaging

The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. However, dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performanc...

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Published inAngewandte Chemie Vol. 132; no. 29; pp. 12252 - 12259
Main Authors Li, Dong‐Hao, Schreiber, Cynthia L., Smith, Bradley D.
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 13.07.2020
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ISSN0044-8249
1521-3757
DOI10.1002/ange.202004449

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Abstract The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. However, dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performance and the scope of possible applications. All these limitations are simultaneously overcome with a new molecular design strategy that produces a charge balanced and sterically shielded fluorochrome. The key design feature is a meso‐aryl group that simultaneously projects two shielding arms directly over each face of a linear heptamethine polyene. Cell and mouse imaging experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjugates) to benchmark heptamethine dyes and found that the shielded systems possess an unsurpassed combination of photophysical, physiochemical, and biodistribution properties that greatly enhance bioimaging performance. It's a bird! It's a plane! Just like a superhero, an ultrastable shielded heptamethine cyanine dye uses its two strong arms to ward off self‐aggregation and non‐specific biological interactions. Yet the arms are short enough to allow dye‐labeled bioconjugates to selectively target cell receptors for high‐contrast and photon‐intense microscopy or tumor imaging in living subjects.
AbstractList The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. However, dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performance and the scope of possible applications. All these limitations are simultaneously overcome with a new molecular design strategy that produces a charge balanced and sterically shielded fluorochrome. The key design feature is a meso‐aryl group that simultaneously projects two shielding arms directly over each face of a linear heptamethine polyene. Cell and mouse imaging experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjugates) to benchmark heptamethine dyes and found that the shielded systems possess an unsurpassed combination of photophysical, physiochemical, and biodistribution properties that greatly enhance bioimaging performance.
The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. However, dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performance and the scope of possible applications. All these limitations are simultaneously overcome with a new molecular design strategy that produces a charge balanced and sterically shielded fluorochrome. The key design feature is a meso ‐aryl group that simultaneously projects two shielding arms directly over each face of a linear heptamethine polyene. Cell and mouse imaging experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjugates) to benchmark heptamethine dyes and found that the shielded systems possess an unsurpassed combination of photophysical, physiochemical, and biodistribution properties that greatly enhance bioimaging performance.
The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. However, dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performance and the scope of possible applications. All these limitations are simultaneously overcome with a new molecular design strategy that produces a charge balanced and sterically shielded fluorochrome. The key design feature is a meso‐aryl group that simultaneously projects two shielding arms directly over each face of a linear heptamethine polyene. Cell and mouse imaging experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjugates) to benchmark heptamethine dyes and found that the shielded systems possess an unsurpassed combination of photophysical, physiochemical, and biodistribution properties that greatly enhance bioimaging performance. It's a bird! It's a plane! Just like a superhero, an ultrastable shielded heptamethine cyanine dye uses its two strong arms to ward off self‐aggregation and non‐specific biological interactions. Yet the arms are short enough to allow dye‐labeled bioconjugates to selectively target cell receptors for high‐contrast and photon‐intense microscopy or tumor imaging in living subjects.
Author Smith, Bradley D.
Li, Dong‐Hao
Schreiber, Cynthia L.
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  givenname: Bradley D.
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  surname: Smith
  fullname: Smith, Bradley D.
  email: smith.115@nd.edu
  organization: University of Notre Dame
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Snippet The near‐infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and...
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SubjectTerms Antibodies
Aromatic compounds
Chemistry
Cyanine dyes
cyanines
Dye penetrants
Dyes
dyes/pigments
Fluorescence
fluorescent probes
imaging agents
Infrared imaging
Infrared windows
Medical imaging
Pharmacokinetics
Physiochemistry
Shielding
Title Sterically Shielded Heptamethine Cyanine Dyes for Bioconjugation and High Performance Near‐Infrared Fluorescence Imaging
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fange.202004449
https://www.proquest.com/docview/2420130256
Volume 132
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