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          <dc:title>Near-Infrared Organic
Structures with Extended Lifetimes
to Unlock the Potential of In Vivo Fluorescence Lifetime
Imaging</dc:title>
          <dc:creator>Elisa Chazeau (14844516)</dc:creator>
          <dc:creator>Hassan Al Sabea (24959044)</dc:creator>
          <dc:creator>Simone Janssen (16982142)</dc:creator>
          <dc:creator>Łukasz Mateusiak (21435797)</dc:creator>
          <dc:creator>Thomas Van den Dries (23142979)</dc:creator>
          <dc:creator>Thomas Lapauw (5210786)</dc:creator>
          <dc:creator>Sevada Sahakian (23142988)</dc:creator>
          <dc:creator>Marcus C.M. Stroet (24959047)</dc:creator>
          <dc:creator>Tim Dreessen (2650801)</dc:creator>
          <dc:creator>Maarten Kuijk (23142994)</dc:creator>
          <dc:creator>Catherine Paul (1585456)</dc:creator>
          <dc:creator>Hans Ingelberts (23142997)</dc:creator>
          <dc:creator>Sophie Hernot (849186)</dc:creator>
          <dc:creator>Anthony Romieu (27583)</dc:creator>
          <dc:creator>Christine Goze (1585465)</dc:creator>
          <dc:creator>Franck Denat (839548)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>short singlet excited</dc:subject>
          <dc:subject>infrared organic structures</dc:subject>
          <dc:subject>fluorescent contrast agents</dc:subject>
          <dc:subject>fluorescent antibody conjugates</dc:subject>
          <dc:subject>conjugation methods impact</dc:subject>
          <dc:subject>lifetime contrast allows</dc:subject>
          <dc:subject>spectrally overlapping fluorophores</dc:subject>
          <dc:subject>fluorescence lifetime imaging</dc:subject>
          <dc:subject>vivo &lt;/ italic</dc:subject>
          <dc:subject>fluorescence imaging</dc:subject>
          <dc:subject>longer lifetime</dc:subject>
          <dc:subject>lifetime differences</dc:subject>
          <dc:subject>lifetime characteristics</dc:subject>
          <dc:subject>fluorescence intensity</dc:subject>
          <dc:subject>vivo &lt;/</dc:subject>
          <dc:subject>tumor imaging</dc:subject>
          <dc:subject>multiplexing imaging</dc:subject>
          <dc:subject>thereby expanding</dc:subject>
          <dc:subject>studies evaluating</dc:subject>
          <dc:subject>state lifetimes</dc:subject>
          <dc:subject>soluble nir</dc:subject>
          <dc:subject>physiological conditions</dc:subject>
          <dc:subject>microenvironmental variations</dc:subject>
          <dc:subject>irdye 800cw</dc:subject>
          <dc:subject>highly successful</dc:subject>
          <dc:subject>extended lifetimes</dc:subject>
          <dc:subject>enhanced sensitivity</dc:subject>
          <dc:subject>emissive aza</dc:subject>
          <dc:subject>bodipy dye</dc:subject>
          <dc:description>&lt;i&gt;In vivo&lt;/i&gt; fluorescence lifetime imaging
(FLI) is
an advanced optical imaging modality with the capability to reveal
additional biological information compared to fluorescence intensity
(FI) imaging. In addition to enabling tissue discrimination based
on microenvironmental variations, lifetime contrast allows the differentiation
of spectrally overlapping fluorophores, thereby expanding the high
potential of multiplexing imaging. Until now, most of the studies
evaluating the benefits of &lt;i&gt;in vivo&lt;/i&gt; FLI in terms of
enhanced sensitivity and specificity for tumor imaging with fluorescent
contrast agents have been conducted using heptamethine cyanine dyes.
While these fluorophores are highly successful for conventional &lt;i&gt;in vivo&lt;/i&gt; fluorescence imaging, they are characterized by
short singlet excited-state lifetimes (generally below 1 ns), making
it challenging to achieve satisfying tissue contrast and to implement
multiplexing imaging strategies based on their lifetime differences.
Here, we report a bioconjugatable, water-soluble NIR-emissive aza-BODIPY
dye with a 100% longer lifetime than IRDye 800CW in physiological
conditions. We demonstrate its suitability for &lt;i&gt;in vivo&lt;/i&gt; FLI when conjugated to cetuximab and reveal how conjugation methods
impact the lifetime characteristics of fluorescent antibody conjugates.</dc:description>
          <dc:date>2026-09-15T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acsomega.6c04430.s002</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Near-Infrared_Organic_Structures_with_Extended_Lifetimes_to_Unlock_the_Potential_of_In_Vivo_Fluorescence_Lifetime_Imaging/33826663</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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