| Literature DB >> 27627995 |
Stefanie Griesbeck1, Zuolun Zhang1,2, Marcus Gutmann3, Tessa Lühmann3, Robert M Edkins1,4, Guillaume Clermont5, Adina N Lazar5, Martin Haehnel1, Katharina Edkins1,6, Antonius Eichhorn1, Mireille Blanchard-Desce7, Lorenz Meinel8, Todd B Marder9.
Abstract
Three water-soluble tetracationic quadrupolar chromophores comprising two three-coordinate boron π-acceptor groups bridged by thiophene-containing moieties were synthesised for biological imaging applications. Compound 3 containing the bulkier 5-(3,5-Me2 C6 H2 )-2,2'-(C4 H2 S)2 -5'-(3,5-Me2 C6 H2 ) bridge is stable over a long period of time, exhibits a high fluorescence quantum yield and strong one- and two-photon absorption (TPA), and has a TPA cross section of 268 GM at 800 nm in water. Confocal laser scanning fluorescence microscopy studies in live cells indicated localisation of the chromophore at the mitochondria; moreover, cytotoxicity measurements proved biocompatibility. Thus, chromophore 3 has excellent potential for one- and two-photon-excited fluorescence imaging of mitochondrial function in cells.Entities:
Keywords: boron; fluorescence; fluorescent probes; imaging agents; nonlinear optics
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Year: 2016 PMID: 27627995 DOI: 10.1002/chem.201602639
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236