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Title: Saccharide sensing molecules having enhanced fluorescent properties

Abstract

The present invention provides formulae for fluorescent compounds that have a number of properties which make them uniquely suited for use in sensors of analytes such as saccharides. The advantageous fluorescent properties include favorable excitation wavelengths, emission wavelengths, fluorescence lifetimes, and photostability. Additional advantageous properties include enhanced aqueous solubility, as well as temperature and pH sensitivity. The compound comprises an aryl or a substituted phenyl botonic acid that acts as a substrate recognition component, a fluorescence switch component, and a fluorophore. Fluorescent compounds are described that are excited at wavelengths greater than 400 nm and emit at wavelengths greater than 450 nm, which is advantageous for optical transmission through skin. The fluorophore is typically selected from transition metal-ligand complexes and thiazine, oxazine, oxazone, or oxazine-one as well as anthracene compounds. The fluorescent compound can be immobilized in a glucose permeable biocompatible polymer matrix that is implantable below the skin.

Inventors:
; ; ; ;
Issue Date:
Research Org.:
Univ. of California, Oakland, CA (United States); MiniMed Inc., Sylmar, CA (United States); Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1174666
Patent Number(s):
6673625
Application Number:
09/823,522
Assignee:
The Regents of the University of California (Oakland, CA); MiniMed Inc. (Sylmar, CA)
Patent Classifications (CPCs):
A - HUMAN NECESSITIES A61 - MEDICAL OR VETERINARY SCIENCE A61B - DIAGNOSIS
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07F - ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
DOE Contract Number:  
W-7405-ENG-48
Resource Type:
Patent
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES

Citation Formats

Satcher Jr., Joe H., Lane, Stephen M., Darrow, Christopher B., Cary, Douglas R., and Tran, Joe Anh. Saccharide sensing molecules having enhanced fluorescent properties. United States: N. p., 2004. Web.
Satcher Jr., Joe H., Lane, Stephen M., Darrow, Christopher B., Cary, Douglas R., & Tran, Joe Anh. Saccharide sensing molecules having enhanced fluorescent properties. United States.
Satcher Jr., Joe H., Lane, Stephen M., Darrow, Christopher B., Cary, Douglas R., and Tran, Joe Anh. Tue . "Saccharide sensing molecules having enhanced fluorescent properties". United States. https://www.osti.gov/servlets/purl/1174666.
@article{osti_1174666,
title = {Saccharide sensing molecules having enhanced fluorescent properties},
author = {Satcher Jr., Joe H. and Lane, Stephen M. and Darrow, Christopher B. and Cary, Douglas R. and Tran, Joe Anh},
abstractNote = {The present invention provides formulae for fluorescent compounds that have a number of properties which make them uniquely suited for use in sensors of analytes such as saccharides. The advantageous fluorescent properties include favorable excitation wavelengths, emission wavelengths, fluorescence lifetimes, and photostability. Additional advantageous properties include enhanced aqueous solubility, as well as temperature and pH sensitivity. The compound comprises an aryl or a substituted phenyl botonic acid that acts as a substrate recognition component, a fluorescence switch component, and a fluorophore. Fluorescent compounds are described that are excited at wavelengths greater than 400 nm and emit at wavelengths greater than 450 nm, which is advantageous for optical transmission through skin. The fluorophore is typically selected from transition metal-ligand complexes and thiazine, oxazine, oxazone, or oxazine-one as well as anthracene compounds. The fluorescent compound can be immobilized in a glucose permeable biocompatible polymer matrix that is implantable below the skin.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Tue Jan 06 00:00:00 EST 2004},
month = {Tue Jan 06 00:00:00 EST 2004}
}

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