Issue 32, 2018

A novel near-infrared and naked-eyes turn on fluorescent probe for detection of biothiols with a large Stokes shift and its application in living cells

Abstract

A novel turn-on fluorescent probe (DDND) for highly selective detection of biothiols over other amino acids was synthesized and investigated in this work, which used the 2,4-dinitrobenzenesulfonyl (DNBS) group as a fluorescent quencher. The novel fluorophore (HDM) features a large π-conjugation system and a typical intramolecular charge transfer (ICT) process and has a long emission wavelength at 623 nm as well as a large Stokes shift (λemλex = 131 nm). Besides that, this red-emitting probe exhibited good linearity ranges with a low detection limit of 0.23 μM for Cys, 0.34 μM for Hcy and 0.41 μM for GSH respectively. Upon titration of thiols, the color of the solution changed from yellow to dark red, which means it can be detected by naked eyes. Finally, probe DDND was successfully applied to bioimage intracellular Cys in HeLa cells with low cytotoxicity.

Graphical abstract: A novel near-infrared and naked-eyes turn on fluorescent probe for detection of biothiols with a large Stokes shift and its application in living cells

Supplementary files

Article information

Article type
Paper
Submitted
14 Jun 2018
Accepted
12 Jul 2018
First published
23 Jul 2018

Anal. Methods, 2018,10, 3991-3999

A novel near-infrared and naked-eyes turn on fluorescent probe for detection of biothiols with a large Stokes shift and its application in living cells

W. Zhang, G. Weijing, T. Cheng, B. Wang, Y. Jiang and J. Shen, Anal. Methods, 2018, 10, 3991 DOI: 10.1039/C8AY01337C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements