Aggregation-induced delayed fluorescence for time-resolved luminescence sensing of carboxylesterase in living cells
An aggregation-induced delayed fluorescence emitter is demonstrated for time-resolved luminescence turn-on sensing of carboxylesterase in living cells. [Display omitted] •The strategy of AIDF-based TRLS was first proposed and realized.•A multiply twisted luminophore revealed typical AIDF behavior.•T...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-06, Vol.437, p.135396, Article 135396 |
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Sprache: | eng |
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Zusammenfassung: | An aggregation-induced delayed fluorescence emitter is demonstrated for time-resolved luminescence turn-on sensing of carboxylesterase in living cells.
[Display omitted]
•The strategy of AIDF-based TRLS was first proposed and realized.•A multiply twisted luminophore revealed typical AIDF behavior.•The turn-on TRLS of carboxylesterase was achieved in buffer and HeLa cells.
Thermally activated delayed fluorescence (TADF) materials with long-lived fluorescent emission, have been considered to be promising candidates for time-resolved luminescence imaging (TRLI) and sensing (TRLS). Though the development of the TADF luminophores for TRLI has received considerable attention, the oxygen-caused delayed fluorescence quenching has greatly stagnated the progress of TADF-based TRLS. In this work, we firstly proposed the strategy of in situ generated aggregation-induced delayed fluorescence (AIDF) for TRLS. A new luminophore FAc-Py with multiply twisted geometry and AIDF behavior was designed to offer the long-lived emission for meeting the time-resolved requirement. The carboxylester-capped FAc-Py, namely FAc-Py-Ester, which is non-emissive but shows good liposolubility, was then rationally synthesized for the delayed fluorescence turn-on sensing of carboxylesterase. Carboxylesterase easily promoted the in situ release of hydrophobic FAc-Py from FAc-Py-Ester, accompanying with the activation of air-insensitive AIDF emission and finally paving a way for the functional TRLS of carboxylesterase in living cells. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2022.135396 |