Literature DB >> 19117043

Bright, color-tunable fluorescent dyes in the Vis/NIR region: establishment of new "tailor-made" multicolor fluorophores based on borondipyrromethene.

Keitaro Umezawa1, Akihiro Matsui, Yuki Nakamura, Daniel Citterio, Koji Suzuki.   

Abstract

A new series of high-performance fluorophores named Keio Fluors (KFL), which are based on borondipyrromethene (BODIPY), are reported. The KFL dyes cover a wide spectral range from the yellow (547 nm) to the near-infrared (NIR, 738 nm) region, and their emission wavelength could be easily and subtly controlled based on simple molecular modifications only, without losing their optical properties. This "tailor-made" synthetic strategy for tuning the emission wavelength enabled the creation of fourteen KFL dyes with well-controlled emission colors (yellow, orange, red, far-red, and NIR). Moreover, these KFL dyes also retain their excellent optical properties, such as spectral bands sharper than quantum dots, high extinction coefficients (140,000-316,000 M(-1) cm(-1)), and high quantum yields (0.56-0.98), without any critical solvent polarity dependent decrease of their brightness. These advantageous characteristics make the KFL dyes potentially useful as new candidates of fluorescent standard dyes to substitute or to complement existing long-wavelength fluorescent dyes, such as cyanines, oxazines, rhodamines, or other BODIPY dyes.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19117043     DOI: 10.1002/chem.200801906

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  32 in total

1.  Semiconductor nanostructures: Two dimensions are brighter.

Authors:  Gregory D Scholes
Journal:  Nat Mater       Date:  2011-11-23       Impact factor: 43.841

2.  Development of UV-excitable red and near-infrared fluorescent labels and their application for simultaneous multicolor bioimaging by single-wavelength excitation.

Authors:  Tetsuya Mizuno; Keitaro Umezawa; Yutaka Shindo; Daniel Citterio; Kotaro Oka; Koji Suzuki
Journal:  J Fluoresc       Date:  2013-05-23       Impact factor: 2.217

Review 3.  BODIPY dyes in photodynamic therapy.

Authors:  Anyanee Kamkaew; Siang Hui Lim; Hong Boon Lee; Lik Voon Kiew; Lip Yong Chung; Kevin Burgess
Journal:  Chem Soc Rev       Date:  2012-09-26       Impact factor: 54.564

4.  Synthesis and Spectroscopic Investigation of a Series of Push-Pull Boron Dipyrromethenes (BODIPYs).

Authors:  Sunting Xuan; Ning Zhao; Xiangyi Ke; Zehua Zhou; Frank R Fronczek; Karl M Kadish; Kevin M Smith; M Graça H Vicente
Journal:  J Org Chem       Date:  2017-02-16       Impact factor: 4.354

Review 5.  NIR dyes for bioimaging applications.

Authors:  Jorge O Escobedo; Oleksandr Rusin; Soojin Lim; Robert M Strongin
Journal:  Curr Opin Chem Biol       Date:  2009-11-18       Impact factor: 8.822

6.  Discovery and early development of squaraine rotaxanes.

Authors:  Jeremiah J Gassensmith; Jeffrey M Baumes; Bradley D Smith
Journal:  Chem Commun (Camb)       Date:  2009-08-24       Impact factor: 6.222

7.  Near infrared fluorescence for image-guided surgery.

Authors:  Summer L Gibbs
Journal:  Quant Imaging Med Surg       Date:  2012-09

8.  Near-infrared molecular probes for in vivo imaging.

Authors:  Xuan Zhang; Sharon Bloch; Walter Akers; Samuel Achilefu
Journal:  Curr Protoc Cytom       Date:  2012-04

Review 9.  Beyond the margins: real-time detection of cancer using targeted fluorophores.

Authors:  Ray R Zhang; Alexandra B Schroeder; Joseph J Grudzinski; Eben L Rosenthal; Jason M Warram; Anatoly N Pinchuk; Kevin W Eliceiri; John S Kuo; Jamey P Weichert
Journal:  Nat Rev Clin Oncol       Date:  2017-01-17       Impact factor: 66.675

10.  Study on Liposomal Encapsulation of New Bodipy Sensitizers for Photodynamic Therapy.

Authors:  Thumuganti Gayathri; A Vijayalakshmi; Sreejith Mangalath; Joshy Joseph; N Madhusudhana Rao; Surya Prakash Singh
Journal:  ACS Med Chem Lett       Date:  2018-02-04       Impact factor: 4.345

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.