Expand this Topic clickable element to expand a topic
Skip to content
Optica Publishing Group
  • Chinese Optics Letters
  • Vol. 14,
  • Issue 6,
  • pp. 061603-
  • (2016)

Preparation of two-photon fluorescent probe and biological imaging application in cells

Not Accessible

Your library or personal account may give you access

Abstract

We report on a novel dibenzothiophene-based two-photon fluorescent probe for selective nuclear bioimaging, which contains bilaterally symmetrical pyridine rings connected by a central conjugated-bridge dibenzothiophene. This probe possesses a large two-photon absorption cross-section of 471 GM, yields a 25-fold enhancement of the fluorescence titration, and a stronger photostability for nuclei labeling than existing probes. The real-time observation period is a minimum of 1800 s under a femtosecond laser excitation, which is significantly longer than that of 4,6-diamidino-2-phenylindole. The above results confirm that this novel molecule is a suitable two-photon fluorescent probe for application to nuclear bioimaging in cells.

© 2016 Chinese Laser Press

PDF Article
More Like This
Two-photon-induced fluorescence of biological markers based on optical fibers

A. Lago, A. T. Obeidat, A. E. Kaplan, J. B. Khurgin, P. L. Shkolnikov, and M. D. Stern
Opt. Lett. 20(20) 2054-2056 (1995)

Folate receptor targeting silica nanoparticle probe for two-photon fluorescence bioimaging

Xuhua Wang, Sheng Yao, Hyo-Yang Ahn, Yuanwei Zhang, Mykhailo V. Bondar, Joseph A. Torres, and Kevin D. Belfield
Biomed. Opt. Express 1(2) 453-462 (2010)

Combined Raman and continuous-wave-excited two-photon fluorescence cell imaging

Natallia Uzunbajakava and Cees Otto
Opt. Lett. 28(21) 2073-2075 (2003)

Cited By

You do not have subscription access to this journal. Cited by links are available to subscribers only. You may subscribe either as an Optica member, or as an authorized user of your institution.

Contact your librarian or system administrator
or
Login to access Optica Member Subscription

Select as filters


Select Topics Cancel
© Copyright 2024 | Optica Publishing Group. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies.