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Stability in Vitamin and Mineral Supplements

a technology of vitamin and mineral supplements and stability, applied in the field of nutritional supplement compositions, can solve the problems of reducing the potency of the affected, undesirable chemical interactions in these complex mixtures, and the inability of the human body to synthesize most of the vitamins and minerals, and achieve the effect of reducing oxidation-induced spotting

Pending Publication Date: 2014-08-07
HALEON US HLDG LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text explains a way to make a multivitamin and mineral tablet without causing oxidation spots. This is done by combining certain metals and vitamins in a way that doesn't create any mobile water.

Problems solved by technology

The human body cannot synthesize most of the vitamins and minerals that are essential to maintaining the health of the human body.
Accordingly, it is not surprising that undesirable chemical interactions can occur in these complex mixtures.
The most common of these reactions are degradation reactions that lead to a reduced potency of the impacted nutrients and may also cause the composition to darken or develop unsightly dark spots.
Both water and fat-soluble vitamin components such as ascorbic acid (vitamin C) and alpha tocopheryl acetate (vitamin E), for example, have been found to be susceptible to moisture induced chemical degradation in multi component supplement compositions.
Ascorbic acid oxidation, promoted by the interaction of ascorbic acid with polyvalent metal ions in a dietary supplement composition and facilitated in the presence of water, can cause tablet darkening and / or spotting and prolonged disintegration times that may impact availability of components for utilization in the body.
However, there are several problems with desiccants: First, desiccants can be physically removed from a package by the consumer negating the beneficial effect.
Secondly, a desiccant may lose efficacy over time and / or have limitations in its ability to remove bound water.
Thirdly, desiccants add expense to the final product.
While this method may mask problems from a consumer's view, the polymeric film coatings used to date do not appreciably reduce spotting and / or darkening problems.
Examination of aged coated tablets often reveals spotting or core darkening under the coating.

Method used

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Examples

Experimental program
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Effect test

example 1

[0043]Three examples of the composition of exemplary embodiments of the invention are provided n Tables 1, 2, and 3. These compositions are representative and examples of the many compositions that are within the scope of the invention and are provided for illustrative purposes. The multi-vitamin and mineral nutritional supplements exemplified in Tables 1-3 are intended to be a daily dosage and typically would be administered in one or more dosage units (e.g. one or more tablets). If multiple dosage units are used they may be taken at one time or spaced intervals during the day. The amounts indicated are of the specified nutrient component and do not include the mass of any counter ions. Accordingly, the specified component may be derived from any pharmaceutically acceptable compound or salt. Further the examples give amounts of nutrients (e.g. vitamins or minerals) and it should be understood that the specified nutrients may be combined with one or more excipients to prepare a fina...

example 2

[0044]Table 4 shows stability data for tablets of an exemplary embodiment of the invention prepared with anhydrous dicalcium phosphate as compared to the same combination of ingredients prepared in the same manner with the exception that dicalcium phosphate dihydrate was used instead of anhydrous dicalcium phosphate. Both sets of tablets comprised 60 mg / tablet Ascorbic Acid (Vitamin C) and 30 IU / tablet Vitamin E and the polyvalent metal cations of 18 mg / tablet iron (as ferrous fumarate), 100 mg / tablet Magnesium (as magnesium oxide), 2 mg / tablet copper (as cupric oxide), 15 mg / tablet zinc (as zinc oxide), 2.5 mg / tablet manganese (as manganese sulfate) 5 mcg / tab Nickel (as nickel sulfate) and 25 mcg / tablet Chromium (as chromium chloride). As indicated above, the only distinction between the two sets of tablets was that one batch was prepared using dicalcium phosphate dihydrate and the other batch was prepared using anhydrous dicalcium phosphate. In both batches the amount of calcium p...

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PUM

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Abstract

The invention provides a multivitamin and mineral nutritional supplement composition comprising at least one polyvalent metal and at least one oxidizable vitamin with substantially improved resistance to reactions that lead to darkening and / or spotting and reactions that may reduce the potency of oxidizable vitamins. The composition is a multivitamin and mineral composition comprising at least one polyvalent metal and at least one oxidizable vitamin wherein the composition is substantially free of mobile bound water. The invention also includes methods for making such a composition and methods of preventing or reducing oxidation, improving the stability of oxidizable vitamins, and stabilizing the disintegration time of a multi-vitamin and mineral nutritional supplement composition.

Description

FIELD OF INVENTION[0001]This invention relates to nutritional supplement compositions. More particularly this invention provides a composition and method to reduce the degradation in vitamin and mineral supplements associated with darkening and / or spotting of multi-component nutritional supplement tablets over time.BACKGROUND OF THE INVENTION[0002]It has long been established that a number of chemical compounds typically referred to as vitamins and minerals provide significant value to maintaining an individual in a healthy state and / or treating specific medical conditions even when supplied in relatively small amounts. The human body cannot synthesize most of the vitamins and minerals that are essential to maintaining the health of the human body. Thus, vitamins and minerals must be obtained from an external source. The two most common external sources are foods and nutritional supplements. As most people do not eat foods that consistently provide the necessary daily requirements o...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K33/42A61K31/07A61K31/59A61K31/355A61K31/51A61K31/525A61K31/455A61K31/4415A61K31/519A61K31/409A61K31/197A61K33/06A61K33/34A61K33/26A61K33/32A61K33/30A61K31/375A23L5/41A23L33/15
CPCA61K33/42A61K33/30A61K31/07A61K31/59A61K31/355A61K31/51A61K31/525A61K31/455A61K31/4415A61K31/519A61K31/409A61K31/197A61K33/06A61K33/34A61K33/26A61K33/32A61K31/375A61K33/00A61K45/06A23V2002/00A61K2300/00A23V2250/702A23V2250/71A23V2250/712A23V2250/708A23V2250/704A23V2250/1578A23V2250/161A23V2250/1588A23V2250/1592A23V2250/1612A23V2250/1642A23V2250/159A23L5/41A23L33/15A23L33/16A61P3/02
Inventor GOLDBERG, ALAN M.DILLS, STEVENMARK, WILLIAMSUTTON, BRUCEBYERLEY, CHAD
Owner HALEON US HLDG LLC
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