IE980887A1 - Anti-oxidant formulations - Google Patents

Anti-oxidant formulations

Info

Publication number
IE980887A1
IE980887A1 IE19980887A IE980887A IE980887A1 IE 980887 A1 IE980887 A1 IE 980887A1 IE 19980887 A IE19980887 A IE 19980887A IE 980887 A IE980887 A IE 980887A IE 980887 A1 IE980887 A1 IE 980887A1
Authority
IE
Ireland
Prior art keywords
formulation
fat
vitamin
tocopherol
oxidant
Prior art date
Application number
IE19980887A
Inventor
Diarmaid Joseph Long
Original Assignee
Diarmaid Joseph Long
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Diarmaid Joseph Long filed Critical Diarmaid Joseph Long
Priority to IE19980887A priority Critical patent/IE980887A1/en
Priority to GB9825719A priority patent/GB2343101B/en
Priority to IE19990789A priority patent/IES990789A2/en
Publication of IE980887A1 publication Critical patent/IE980887A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • A23L3/3481Organic compounds containing oxygen
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • A23L3/3481Organic compounds containing oxygen
    • A23L3/3508Organic compounds containing oxygen containing carboxyl groups
    • A23L3/3517Carboxylic acid esters
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • A23L3/3544Organic compounds containing hetero rings
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0092Mixtures

Abstract

A formulation used in assisting in the prevention of oxidation in the fat phase, particularly in food preparations containing poly-unsaturated fatty compounds, fat-soluble vitamins and natural colourants, characterised in that said formulation comprises a delta tocopherol homologue and an ascorbyl moiety. The formulation is a fat-soluble synergistic anti-oxidant formulation producible in a 'one pot' reaction vessel, which can utilise heat to increase the dispersion of the formulation.

Description

ANTI-OXIDANT FORMULATIONS present invention relates to anti-oxidant formulations. Anti-oxidants are well known substances and are found in many of the foods we eat. Anti-oxidants are used to stabilise constituents in food as such constituents can be prone to oxidation and if oxidation occurs, the quality of the food can be adversely affected. Anti-oxidants are also useful as part of a healthy diet and provide a number of physiological benefits to a consumer. As a result consumers look for the presence of antioxidants in the products they use today.
One such anti-oxidant is the naturally occurring vitamin E (Tocopherol). Vitamin E is naturally fat-soluble. Vegetable oil naturally contains vitamin E however this vitamin E is lost during the purification process used in the production of vegetable oil. Therefore it is useful to add an appropriate amount of vitamin E to the purified vegetable oil to replace what was lost during the purification process. Vegetable oils are rich in unsaturated fatty acids, which require anti-oxidants to prevent oxidation.
Q δ UJ n. w co CM LL' C£ £E P O LU & -j Q < 03 S’ O p G ·· ·'· c Fat soluble vitamins A, D and beta-carotene are very susceptible to oxidation. The addition of vitamin E to products containing these fat-soluble vitamins will prevent their oxidation and therefore enhance the properties of the product in which they are contained.
Some of the colourants used in food today can undergo discolouration due to oxidation -^^^ipsulting in a decrease in their commercial value. Vitamin E can also assist in reducing J fhis discolouration. < X! I IThe effectiveness of vitamin E can be enhanced by the use of a synergist. An example of a 9 jjJ kvhich is vitamin C. As vitamin E works to prevent oxidation of fats, oils etc. it is itself • foxidised and as a result loses its anti-oxidant ability. In the presence of vitamin C (ascorbic jH jacid), vitamin E is regenerated by reduction and is then available to resume its anti-oxidant \« j effect. a jj a J a J O } However at present, the combined use of vitamin E and vitamin C is hampered in that ΣΙ ι ,3 | naturally occurring vitamin C is water-soluble and not at all fat-soluble. This reduces the , L versatility of the synergistic combination of vitamin E and vitamin C. -2In an effort to overcome this problem, research has been carried out into various methods of dissolving vitamin C into fat-soluble systems. The use of micro-emulsions sometimes referred to as ‘reversed micelles’ is one such method. Research work carried out in this area was in relation to fish oil and the solvation of vitamin C (JAOCS, Vol.68 No. 10 (Oct. 1991) Daeseok Han, Ock-Sook Yi and Hyun-Kyuny Shin). This system uses water and lecithin along with the fish oil. This combination allows for vitamin C to be dissolved in the fish oil and in turn act as an synergist to vitamin E. There are other chemicals which can be used as surfactants to dissolve vitamin C instead of lecithin for example dioctyl sodium sulfosuccinate and cetylbrimethyl ammonium bromide. By using any of the above synthetic chemicals, further additives are being introduced which are usually expensive and sometimes undesirable from the point of view of the customer.
It is an object of the present invention to alleviate the problems associated with the prior art.
The present invention accordingly provides formulations used in assisting in the prevention of oxidation in the fat phase, particularly in food preparations containing poly-unsaturated fatty compounds, fat-soluble vitamins and natural colourants, characterised in that said formulation comprises a delta tocopherol homologue and an ascorbyl moiety.
Preferably the delta tocopherol homologue and ascorbyl moiety are present in a ratio of 0.1 to 100 when expressed in the form; Weight of d-delta tocopherol Weight of ascorbyl moiety 25 Advantageously the tocopherol homologue is a delta isomer of tocopherol and the ascorbyl moiety is L-ascorbyl palmitate.
Conveniently the formulation is a fat-soluble synergistic anti-oxidant formulation 30 producible in a ‘one pot’ reaction vessel which can utilise heat to increase the dispersion of the formulation. -3Preferably a method for producing the formulation involves a dispersing agent used to improve the dispersion of the components of said formulation which is removable at the end of the production process under vacuum.
The synergistic formulation is usable in fat phase (non-aqueous) systems due to the solubility of the compounds used. Vitamin E is naturally fat-soluble and the vitamin C (ascorbyl moiety) is in the form of a palmitate ester, which is fat-soluble.
D-delta Tocopherol is the most potent homologue of the fat-soluble naturally occurring forms of vitamin E and its properties as an anti-oxidant are well known. As a consequence of the anti-oxidant activity of d-delta Tocopherol, it is itself oxidised. In order to extend the life of d-delta Tocopherol a second element is required. Vitamin C (ascorbic acid) is a compound that can increase the working life of d-delta Tocopherol as an anti-oxidant. By using palmitate ester of vitamin C the ascorbic moiety is capable of regenerating oxidised d-delta Tocopherol in the fat phase by reduction of the oxidised d-delta Tocopherol it can then resume its anti-oxidant activity.
The present invention will now be described fully with reference to the following nonlimiting examples, which are given by way of example only.
Examples Example 1.
The formulation for the anti-oxidant can be dispensed in an ampoule form for a dedicated application. The ingredients are used in the following amounts; Ingredient_Amount d-delta Tocopherol 29gms L-ascorbyl palmitate 70gms The ingredients are combined in a high-speed blender. The mixing vessel is warmed to 100° to increase dispersion of the formulation mixture and the formulation is dispensed into the ampoules as required Example 2. -4A dispersing agent for example ethanol and a solubilising agent, for example distilled monoglyceride at an approximate level of 0.25% W/W of the ascorbyl palmitale used are mixed with d-delta Tocopherol. This mixture is then blended (homogenised) with the ascorbyl moiety. The dispersing agent is removed under vacuum at the end of the process.
The formulation can then be packed into ampoules as required.
Example 3.
The formulation of d-delta tocopherol and ascorbyl palmitate are dispensed separately but in the ratio outlined example 1 into separate compartments of an ampoule, allowing for separate dispensation to liquid and solid components of a users process before eventual combination to form the synergistic mixture.
It will of course be understood that the invention is not limited to the specific details described herein, which are given by way of example only, and that various modifications and alterations are possible within the scope of the invention as defined in the appended claims.

Claims (7)

Claims
1. A formulation useful in assisting in the prevention of oxidation in the fat phase, characterised in that said formulation comprises a delta tocopherol homologue and an ascorbyl moiety.
2. A formulation as claimed in claim 1 wherein the delta tocopherol homologue and ascorbyl moiety are present in a ratio of 0.1 to 100 when expressed in the form: Weight of d-delta tocopherol Weight of ascorbyl moiety
3. A formulation as claimed in claim 1 wherein the tocopherol homologue is a delta isomer of tocopherol.
4. A formulation as claimed in claim 1 wherein the ascorbyl moiety is L-ascorbyl palmitate.
5. A formulation as claimed in any one of the preceding claims wherein the formulation is a fat-soluble synergistic anti-oxidant formulation which can be produced as a “one pot” formulation.
6. A method for producing a formulation as claimed in claim 1 wherein a dispersing agent is used to improve the dispersion of the components of said formulation, the method including the step of removing the dispersing agent after it has performed its function.
7. A method as claimed in claim 6 wherein the dispersion agent is removed under vacuum.
IE19980887A 1998-10-27 1998-10-27 Anti-oxidant formulations IE980887A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
IE19980887A IE980887A1 (en) 1998-10-27 1998-10-27 Anti-oxidant formulations
GB9825719A GB2343101B (en) 1998-10-27 1998-11-25 Anti-oxidant formulations
IE19990789A IES990789A2 (en) 1998-10-27 1999-09-22 Anti-oxidant formulations

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IE19980887A IE980887A1 (en) 1998-10-27 1998-10-27 Anti-oxidant formulations

Publications (1)

Publication Number Publication Date
IE980887A1 true IE980887A1 (en) 2000-05-03

Family

ID=11041917

Family Applications (2)

Application Number Title Priority Date Filing Date
IE19980887A IE980887A1 (en) 1998-10-27 1998-10-27 Anti-oxidant formulations
IE19990789A IES990789A2 (en) 1998-10-27 1999-09-22 Anti-oxidant formulations

Family Applications After (1)

Application Number Title Priority Date Filing Date
IE19990789A IES990789A2 (en) 1998-10-27 1999-09-22 Anti-oxidant formulations

Country Status (2)

Country Link
GB (1) GB2343101B (en)
IE (2) IE980887A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0026018D0 (en) 2000-10-24 2000-12-13 Novartis Nutrition Ag New composition
US9132117B2 (en) 2013-06-17 2015-09-15 Kgk Synergize, Inc Compositions and methods for glycemic control of subjects with impaired fasting glucose

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK136039B (en) * 1970-09-08 1977-08-01 Kongo Yakuhin Kabushiki Kaisha Method and means for preventing oxidation of lipids and / or dyes which are or are to be included in foodstuffs.
DE3500938A1 (en) * 1985-01-14 1986-07-17 Henkel KGaA, 4000 Düsseldorf STABILIZATION OF PALM CORE OIL AND PALM CORE FATTY ACID ALKYL ESTERS FOR THEIR PROCESSING TO COLOR-NEUTRAL REACTION PRODUCTS
US5102659A (en) * 1990-07-12 1992-04-07 Shaklee Corporation Natural antioxidant compositions
US5234702A (en) * 1992-03-19 1993-08-10 Abbott Laboratories Antioxidant system for powdered nutritional products

Also Published As

Publication number Publication date
GB2343101A (en) 2000-05-03
GB2343101B (en) 2002-11-20
GB9825719D0 (en) 1999-01-20
IES990789A2 (en) 2000-07-12

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