Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

The location of phenolic antioxidants and radicals at interfaces determines their activity.

The location of phenolic antioxidants and radicals at interfaces determines their activity. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • The location of phenolic antioxidants and radicals at interfaces determines their activity. Abstract Text:

    anja heinsAnja Heins,donald b mcphailDonald B McPhail,tobias sokolowskiTobias Sokolowski,heiko Heiko ,karin schwarzKarin Schwarz,anja heinsAnja Heins,donald b mcphailDonald B McPhail,tobias sokolowskiTobias Sokolowski,heiko Heiko ,karin schwarzKarin Schwarz,

    To characterize parameters influencing the antioxidant activity at interfaces a novel ESR approach was developed, which facilitates the investigation of the reaction stoichiometry of antioxidants towards stable radicals. To relate the activity of antioxidants towards the location of radicals at interfaces NMR experiments were conducted. Micellar solutions of SDS, Brij and CTAB were used to model interfaces of different chemical nature. The hydrophilic Fremy's radical was found to be solubilized exclusively in the aqueous phase of SDS micellar solution but partitioned partly into the hydrophilic headgroup area of Brij micelles. In contrast the hydrophobic galvinoxyl was exclusively located in the micellar phase with the increasing depth of intercalation in the order SDS < Brij < CTAB. Gallates revealed a higher stoichiometric factor towards galvinoxyl in CTAB systems, which is accounted to a concentration effect of antioxidant and radical being both solubilized in the palisade layer. In contrast, in SDS solutions hardly any reaction between galvinoxyl and gallates was found. SDS acted as a physical barrier between radical (palisade layer) and antioxidant (stern layer). The influence of the hydrophobic properties of the antioxidant was clearly seen in Brij micelles. Elongation of the alkyl chain in gallate molecule resulted in increasing stoichiometric factors in the presence of galvinoxyl being located in the deeper region of the bulky headgroup area. The reverse trend was found in the presence of Fremy's radical being located in the hydrated area of the micelles.

    The location of phenolic antioxidants and radicals at interfaces determines their activity. Publishing Authors By Initials

    a heinsA Heins,db mcphailDB McPhail,t sokolowskiT Sokolowski,h H ,k schwarzK Schwarz,a heinsA Heins,db mcphailDB McPhail,t sokolowskiT Sokolowski,h H ,k schwarzK Schwarz,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    The location of phenolic antioxidants and radicals at interfaces determines their activity. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Lipids

    VOLUME: 42

    Page Numbers: 573-82

    Journal Abbreviation: Lipids

    ISSN: 0024-4201

    DAY: 1

    MONTH: 05

    YEAR: 2007

    The location of phenolic antioxidants and radicals at interfaces determines their activity. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 60450

    The location of phenolic antioxidants and radicals at interfaces determines their activity. Keywords Mesh Terms:

    KEYWORDS:

    MESH TERMS:

    Chemical & Substance for Abstract: The location of phenolic antioxidants and radicals at interfaces determines their activity. Information

    Substance Name:

    Registry Number:

    Grant and Affiliation Information for The location of phenolic antioxidants and radicals at interfaces determines their activity.

    AFFILIATION: Institute of Human Nutrition and Food Science, University of Kiel, Heinrich-Hecht-Platz 10, 24118 Kiel, Germany. info@foodtech.uni-kiel.de

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Lipids

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    The location of phenolic antioxidants and radicals at interfaces determines their activity Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News