2017Methods and Applications in FluorescenceOpen access

Development of a novel europium complex-based luminescent probe for time-gated luminescence imaging of hypochlorous acid in living samples

Xiangli Liu, Lianying Guo, Bo Song, Zhixin Tang, Jingli Yuan

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Abstract

Abstract Luminescent lanthanide complexes are key reagents used in the time-gated luminescence bioassay technique, but functional lanthanide complexes that can act as luminescent probes for specifically responding to analytes are very limited. In this work, we designed and synthesized a novel Eu 3+ complex-based luminescence probe for hypochlorous acid (HOCl), NPPTTA-Eu 3+ , by using terpyridine polyacid-Eu 3+ , dinitrophenyl, and hydrazine as luminophore, quencher and HOCl-recognizer moieties, respectively. In the absence of HOCl, the probe is non-luminescent due to the strong luminescence quenching of the dinitrophenyl group in the complex. However, upon reaction with HOCl, the dinitrophenyl moiety is rapidly cleaved from the probe, which affords a strongly luminescent Eu 3+ complex CPTTA-Eu 3+ , accompanied by a ∼900-fold luminescence enhancement with a long luminescence lifetime of 1.41 ms. This unique luminescence response of NPPTTA-Eu 3+ to HOCl allowed NPPTTA-Eu 3+ to be conveniently used as a probe for highly selective and sensitive detection of HOCl under the time-gated luminescence mode. In addition, by loading NPPTTA-Eu 3+ into RAW 264.7 macrophage cells and Daphnia magna , the generation of endogenous HOCl in RAW 264.7 cells and the uptake of exogenous HOCl by Daphnia magna were successfully imaged on a true-color time-gated luminescence microscope. The results demonstrated the practical applicability of NPPTTA-Eu 3+ as an efficient probe for time-gated luminescence imaging of HOCl in living cells and organisms.

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Abstract Luminescent lanthanide complexes are key reagents used in the time-gated luminescence bioassay technique, but functional lanthanide complexes that can act as luminescent probes for specifically responding to analytes are very limited. In this work, we designed and synthesized a novel Eu 3+ complex-based luminescence probe for hypochlorous acid (HOCl), NPPTTA-Eu 3+ , by using terpyridine polyacid-Eu 3+ , dinitrophenyl, and hydrazine as luminophore, quencher and HOCl-recognizer moieties, respectively. In the absence of HOCl, the probe is non-luminescent due to the strong luminescence quenching of the dinitrophenyl group in the complex. However, upon reaction with HOCl, the dinitrophenyl moiety is rapidly cleaved from the probe, which affords a strongly luminescent Eu 3+ complex CPTTA-Eu 3+ , accompanied by a ∼900-fold luminescence enhancement with a long luminescence lifetime of 1.41 ms. This unique luminescence response of NPPTTA-Eu 3+ to HOCl allowed NPPTTA-Eu 3+ to be conveniently used as a probe for highly selective and sensitive detection of HOCl under the time-gated luminescence mode. In addition, by loading NPPTTA-Eu 3+ into RAW 264.7 macrophage cells and Daphnia magna , the generation of endogenous HOCl in RAW 264.7 cells and the uptake of exogenous HOCl by Daphnia magna were successfully imaged on a true-color time-gated luminescence microscope. The results demonstrated the practical applicability of NPPTTA-Eu 3+ as an efficient probe for time-gated luminescence imaging of HOCl in living cells and organisms.

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Available abstract

Abstract Luminescent lanthanide complexes are key reagents used in the time-gated luminescence bioassay technique, but functional lanthanide complexes that can act as luminescent probes for specifically responding to analytes are very limited. In this work, we designed and synthesized a novel Eu 3+ complex-based luminescence probe for hypochlorous acid (HOCl), NPPTTA-Eu 3+ , by using terpyridine polyacid-Eu 3+ , dinitrophenyl, and hydrazine as luminophore, quencher and HOCl-recognizer moieties, respectively. In the absence of HOCl, the probe is non-luminescent due to the strong luminescence quenching of the dinitrophenyl group in the complex. However, upon reaction with HOCl, the dinitrophenyl moiety is rapidly cleaved from the probe, which affords a strongly luminescent Eu 3+ complex CPTTA-Eu 3+ , accompanied by a ∼900-fold luminescence enhancement with a long luminescence lifetime of 1.41 ms. This unique luminescence response of NPPTTA-Eu 3+ to HOCl allowed NPPTTA-Eu 3+ to be conveniently used as a probe for highly selective and sensitive detection of HOCl under the time-gated luminescence mode. In addition, by loading NPPTTA-Eu 3+ into RAW 264.7 macrophage cells and Daphnia magna , the generation of endogenous HOCl in RAW 264.7 cells and the uptake of exogenous HOCl by Daphnia magna were successfully imaged on a true-color time-gated luminescence microscope. The results demonstrated the practical applicability of NPPTTA-Eu 3+ as an efficient probe for time-gated luminescence imaging of HOCl in living cells and organisms.

Key concepts: Luminescence, Hypochlorous acid, Chemistry, Luminescent Measurements, Photochemistry, Quenching (fluorescence), Fluorescence, Materials science

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