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οƒ˜ Phytic acid is used widely as a food
  additive in Japan.
οƒ˜ It is a yellow color liquid that
  decomposes on heating.
οƒ˜   Empirical formula: C6H18O24P6
οƒ˜   Molecular weight:660.08
οƒ˜   physical appearance: Yellow colored
    liquid
οƒ˜   Solubility: Miscible with water, 95% ethyl
    alcohol, glycerol.
οƒ˜   Toxicity: Oral rat LD50: >90 ml/kg.
οƒ˜   Stability: Stable under ordinary
    conditions.
οƒ˜   At low pH it precipitates iron
    quantitatively
οƒ˜   At higher pH it forms insoluble complexes
    with all other polyvalent cations.
οƒ˜   Some of the important physiological
    function-of phytic acid include storage
    of phosphorus, high-energy phosphate
    groups, am; cations, and protection of
    seeds against oxidative damage during
    storage.
οƒ˜   The antioxidant functions of phytic acid have been
    described by Graf and Eaton
οƒ˜   Phytic acid has a relatively high binding affinity for iron and
    is a potent inhibitor of iron-mediated hydroxyl radical
    formation.
οƒ˜   In the absence of phytate, Fe + is completely insoluble at
    neutral or higher pH due to the formation of large
    polynuclear iron hydroxide complexes.
οƒ˜   High concentrations of phytic acid solubilize iron in the form
    of Fe(III) 1-phytate, whereas low concentration precipitate
    iron as Fe(III)3- and Fe(III)4-phytate complexes.
οƒ˜   Chelating of iron by phytic acid prevents the formation of
    polynuclear aggregates even at iron concentrations as low
    as 6 nM.
οƒ˜   The six coordination sites of trivalent iron are occupied by
    water and hydroxide ions in aqueous solutions.
οƒ˜   Most chelating agent displace five of these ligands and
    form a pentadentate chelate with H2O occupying the
    sixth coordination site.
οƒ˜   Phytic acid, however, is unique in occupying six
    coordination sites and displacing all of the coordination
    water in the Fe(III)complex.
οƒ˜   Iron-catalyzed formation of hydroxyl radical requires the
    availability of at least one reactive iron coordination site
    as well as iron solubility.
οƒ˜   Phytic acid preserves the solubility and makes the metal
    totally enactive.
οƒ˜   In molar phytate-to-iron ratios of 0.25 and above, the
    supcroxidc-driven generation c: hydroxyl radical is
    completely blocked.
οƒ˜   Phytic acid appears to be one of the most effective agents
    for the inhibition of iron-mediated lipid oxidation in foot
    products.
οƒ˜   In meat products, it presumably removes myoglobin-derived
    iron froivi negatively charged phospholipids and prevents
    their autoxidation and off-flavor formation.
οƒ˜   Phytic acid substantially inhibits oxygen uptake,
    malondialdehyde formation, and warmed-over flavor
    development in cooked minced chicken breasts stored in
    sealed oxygen-impermeable containers at 4Β°C.
οƒ˜   In a soybean oil-in-water emulsion system, the oxidation was
    significantly decreased by the addition of 1M phytic acid.
οƒ˜   Phytic acid also significantly reduces the iron-catalyzed
    oxidation and partially inhibits the copper-mediated
    oxidation of ascorbic acid in model systems
οƒ˜   Phospholipids or phosphatides occur in all living organisms
    and make up l-2% of many crude oils and animal fats.
οƒ˜   The term lecithin was initially used for crude fractions of
    phospholipids obtained from vegetable oils or fats.
οƒ˜   At present it is used to refer to phosphatidylcholine (l,2-
    diacylglycero-3-phosphorylcholinc).
οƒ˜   It is also used to describe soybean lecithin, which is
    composed of soybean-phosphatides and soybean oil.
οƒ˜   Chemically, phosphatidylcholine consists of a glyceride in
    which two of the hydroxyl groups are esterified with fatty
    acids and the third is verified with a phosphoric acid that
    in turn is bound to a molecule of choline. In
    phosphatidylethanolamine, the choline is replaced by
    ethanolamine.
οƒ˜   The commercial source of lecithin is mainly soybeans.
οƒ˜   Some of the parameters that characterize commercial
    lecithin are acetone-insoluble matter, acid value,
    moisture content, hexane-insoluble matter, color,
    consistency, and clarity.
οƒ˜   Commercial lecithin insists of about 66% phospholipids, the
    other major components being the glycerides.
οƒ˜   Lecithin is classified as plastic or fluid according to its viscosity.
οƒ˜   Each of these is further classified into natural, bleached, or
    unbleached grades based on color.
οƒ˜   Only the unbleached grades are permitted as food additives.
οƒ˜   Commercial lecithin can also be produced as a powder by
    alcohol or acetone extractions.
οƒ˜   It is soluble in oils and is hydrated in water with the formation
    of an emulsion.
οƒ˜   The phospholipids function synergistically with primary
    antioxidants, especially the tocopherols, in stabilizing various
    fats and oils.
οƒ˜   Lecithin also functions as a carrier for antioxidants such as PG
    in commercial mixtures.
οƒ˜   Commercial mixtures containing lecithin, a-tocopherol, and
    ascorblypalmitate or ascorbic acid are available.
οƒ˜   In such mixtures, ascorbic acid regenerates tocopherol
    mediated by lecithin.
οƒ˜   However, the mechanism is not understood.
οƒ˜   The various applications of the synergistic mixtures have been
    described here under the food applications of toeopherols.
ο‚ž   Thank you

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Chelating agents

  • 1.
  • 2. οƒ˜ Phytic acid is used widely as a food additive in Japan. οƒ˜ It is a yellow color liquid that decomposes on heating.
  • 3. οƒ˜ Empirical formula: C6H18O24P6 οƒ˜ Molecular weight:660.08 οƒ˜ physical appearance: Yellow colored liquid οƒ˜ Solubility: Miscible with water, 95% ethyl alcohol, glycerol. οƒ˜ Toxicity: Oral rat LD50: >90 ml/kg. οƒ˜ Stability: Stable under ordinary conditions.
  • 4. οƒ˜ At low pH it precipitates iron quantitatively οƒ˜ At higher pH it forms insoluble complexes with all other polyvalent cations. οƒ˜ Some of the important physiological function-of phytic acid include storage of phosphorus, high-energy phosphate groups, am; cations, and protection of seeds against oxidative damage during storage.
  • 5. οƒ˜ The antioxidant functions of phytic acid have been described by Graf and Eaton οƒ˜ Phytic acid has a relatively high binding affinity for iron and is a potent inhibitor of iron-mediated hydroxyl radical formation. οƒ˜ In the absence of phytate, Fe + is completely insoluble at neutral or higher pH due to the formation of large polynuclear iron hydroxide complexes. οƒ˜ High concentrations of phytic acid solubilize iron in the form of Fe(III) 1-phytate, whereas low concentration precipitate iron as Fe(III)3- and Fe(III)4-phytate complexes. οƒ˜ Chelating of iron by phytic acid prevents the formation of polynuclear aggregates even at iron concentrations as low as 6 nM. οƒ˜ The six coordination sites of trivalent iron are occupied by water and hydroxide ions in aqueous solutions.
  • 6. οƒ˜ Most chelating agent displace five of these ligands and form a pentadentate chelate with H2O occupying the sixth coordination site. οƒ˜ Phytic acid, however, is unique in occupying six coordination sites and displacing all of the coordination water in the Fe(III)complex. οƒ˜ Iron-catalyzed formation of hydroxyl radical requires the availability of at least one reactive iron coordination site as well as iron solubility. οƒ˜ Phytic acid preserves the solubility and makes the metal totally enactive. οƒ˜ In molar phytate-to-iron ratios of 0.25 and above, the supcroxidc-driven generation c: hydroxyl radical is completely blocked.
  • 7. οƒ˜ Phytic acid appears to be one of the most effective agents for the inhibition of iron-mediated lipid oxidation in foot products. οƒ˜ In meat products, it presumably removes myoglobin-derived iron froivi negatively charged phospholipids and prevents their autoxidation and off-flavor formation. οƒ˜ Phytic acid substantially inhibits oxygen uptake, malondialdehyde formation, and warmed-over flavor development in cooked minced chicken breasts stored in sealed oxygen-impermeable containers at 4Β°C. οƒ˜ In a soybean oil-in-water emulsion system, the oxidation was significantly decreased by the addition of 1M phytic acid. οƒ˜ Phytic acid also significantly reduces the iron-catalyzed oxidation and partially inhibits the copper-mediated oxidation of ascorbic acid in model systems
  • 8. οƒ˜ Phospholipids or phosphatides occur in all living organisms and make up l-2% of many crude oils and animal fats. οƒ˜ The term lecithin was initially used for crude fractions of phospholipids obtained from vegetable oils or fats. οƒ˜ At present it is used to refer to phosphatidylcholine (l,2- diacylglycero-3-phosphorylcholinc). οƒ˜ It is also used to describe soybean lecithin, which is composed of soybean-phosphatides and soybean oil. οƒ˜ Chemically, phosphatidylcholine consists of a glyceride in which two of the hydroxyl groups are esterified with fatty acids and the third is verified with a phosphoric acid that in turn is bound to a molecule of choline. In phosphatidylethanolamine, the choline is replaced by ethanolamine. οƒ˜ The commercial source of lecithin is mainly soybeans.
  • 9.
  • 10. οƒ˜ Some of the parameters that characterize commercial lecithin are acetone-insoluble matter, acid value, moisture content, hexane-insoluble matter, color, consistency, and clarity. οƒ˜ Commercial lecithin insists of about 66% phospholipids, the other major components being the glycerides. οƒ˜ Lecithin is classified as plastic or fluid according to its viscosity. οƒ˜ Each of these is further classified into natural, bleached, or unbleached grades based on color. οƒ˜ Only the unbleached grades are permitted as food additives. οƒ˜ Commercial lecithin can also be produced as a powder by alcohol or acetone extractions. οƒ˜ It is soluble in oils and is hydrated in water with the formation of an emulsion.
  • 11. οƒ˜ The phospholipids function synergistically with primary antioxidants, especially the tocopherols, in stabilizing various fats and oils. οƒ˜ Lecithin also functions as a carrier for antioxidants such as PG in commercial mixtures. οƒ˜ Commercial mixtures containing lecithin, a-tocopherol, and ascorblypalmitate or ascorbic acid are available. οƒ˜ In such mixtures, ascorbic acid regenerates tocopherol mediated by lecithin. οƒ˜ However, the mechanism is not understood. οƒ˜ The various applications of the synergistic mixtures have been described here under the food applications of toeopherols.
  • 12. ο‚ž Thank you