期刊
JOURNAL OF MATERIALS CHEMISTRY B
卷 5, 期 12, 页码 2322-2329出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7tb00345e
关键词
-
资金
- Department of Education of Liaoning Province [L201683668]
Although considerable efforts have been made for the development of lanthanide complex-based luminescent probes, a major drawback of the current probes is the requirement for UV excitation. In this work, a visible-light-excited Eu3+ complex-based luminescent probe, [Eu(HDPH)(3)(DPBT)] (HDPH: 1,1,1,2,2,3,3heptafluoro- 6-(2,4-dimethoxyphenyl)-4,6-hexanedione; DPBT: 2-(N,N-diethylanilin-4-yl)-4,6-bis(3,5dimethylpyrazol- 1-yl)-1,3,5-triazine), has been designed and synthesized for the highly sensitive and selective time-gated luminescence imaging detection of peroxynitrite (ONOO-) in living cells. The probe exhibits a strong visible excitation peak at 400 nm, with the excitation window extending to beyond 460 nm. Upon reaction with ONOO-, the luminescence of the probe at 610 nm is greatly quenched because the excited state of the Eu3+ complex is deactivated by the interaction between the 2,4-dimethoxyphenyl moiety and ONOO-. The dose-dependent luminescence decrease of the probe shows good linearity with a detection limit of 1.8 mu M for ONOO-, and the probe can specifically distinguish ONOO- from other reactive oxygen/nitrogen species (ROS/RNS). The [Eu(HDPH) 3(DPBT)]-loaded HepG2 cells were prepared, and then the exogenous ONOO- in HepG2 cells was successfully imaged in timegated luminescence mode. The photostability results of the [Eu(HDPH) 3(DPBT)]-loaded HepG2 cells demonstrate the practical applicability of the visible-light-excited probes for long-term cell imaging.
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