Literature DB >> 34116417

A novel 1,8-naphthalimide-based Cu2+ ion fluorescent probe and its bioimaging application.

Jianhua Wei1, Hao Sun1, Yan Jiang1, Baoxi Miao1, Xiang'en Han2, Yun Zhao1, Zhonghai Ni3.   

Abstract

A new 1,8-naphthalimide-based Schiff base compound, named as (Z)-2-butyl-6-(((2-hydroxyphenyl)imino)methyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione (BHBD), has been simply synthesized with high yields. BHBD can be employed as a "turn-on" fluorescent probe for Cu2+ ion with high sensitivity, high selectivity and relatively low detection limit (0.48 × 10-6 M). The fluorescence emission of BHBD is very weak in H2O/THF (v/v: 7/3) mixture, which is significantly enhanced after addition of Cu2+ ion. The proposed mechanism is verified by 1H NMR, Job's plot and TOF-MS experiments. Anti-interference experiment, cytotoxicity assay and pH influence results indicated that BHBD meets the requirements of bioimaging. Therefore, BHBD has been successfully applied in detecting Cu2+ ion in HeLa cells.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bioimaging; Fluorescent probe; Naphthalimide

Year:  2021        PMID: 34116417     DOI: 10.1016/j.saa.2021.120037

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  1 in total

1.  The Schiff Base Probe With J-aggregation Induced Emission for Selective Detection of Cu2.

Authors:  Meihui Chen; Fengying Cao; Shizhou Huang; Yangping Li; Min Zhong; Mingguang Zhu
Journal:  J Fluoresc       Date:  2022-04-22       Impact factor: 2.525

  1 in total

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