Chewing cum capable of releasing finely divided water-insoluble materials therefrom

• US 4,238,475 A
• Filed: 08/01/1979
• Issued: 12/09/1980
• Est. Priority Date: 08/01/1979
• Status: Expired due to Term

• Current Assignee: Nabisco Technology Company (Mondelez International, Inc.)
• Original Assignee: Life Savers Incorporated (Mondelez International, Inc.)
• Inventors: Witzel, Frank, Puglia, Wayne J., Clark, K. Warren, Mackay, Donald A. M.
• Primary Examiner(s): Rose, Shep K.
• Application Number:
  US06/062,861
• Time in Patent Office: 496 Days
• Field of Search: 426/3-6, 424/48
• US Class Current: 424/48
• CPC Class Codes: A23G 4/06 characterised by the composition containing organic or inorganic compounds
• CPC Class Codes: A23G 4/126 containing vitamins, antibiotics
• CPC Class Codes: A23G 4/20 Composite products, e.g. centre-filled , multi-layer, laminated
• CPC Class Codes: A61K 9/0058 Chewing gums non-medicinal aspects, preparing chewing gum A23G4/00; chewing gum for care of the teeth or oral cavity, e.g. with breath freshener A61Q11/00

Abstract

A chewing gum is provided which is capable of releasing into the oral cavity relatively large amounts of finely-divided water-insoluble therapeutic materials, which chewing gum includes a water-soluble phase formed of aqueous softener, and the finely divided therapeutic component to be released, said therapeutic component being coated with a water-soluble coating agent for preventing resorption of therapeutic component back into the gum base and, optionally, a first sweetener, dispersed throughout the aqueous softener, and a relatively water-insoluble phase formed of a plurality of separate and distinct masses suspended in and dispersed throughout the water-soluble phase, each of said masses formed of particles of gum base and, optionally, particles of a second sweetener, suchas mannitol and/or sorbitol or sugar, enveloped by particles of gum base. Upon chewing the above gum, the therapeutic component is, in fact, released in the oral cavity in relatively large quantities, together with the aqueous softener.

The therapeutic component to be released may comprise orally beneficial materials, such as dicalcium phosphate, antacids, such as magnesium hydroxide, calcium carbonate, as well as vitamins, drugs and the like. In a preferred embodiment, the therapeutic component is coated with gum arabic to facilitate release from chewing gum.

Claims

1. A chewing gum capable of releasing finely divided water-insoluble therapeutic materials therefrom comprising a water-soluble phase comprised of softener, a finely divided water-insoluble therapeutic material coated with a water-soluble coating agent to facilitate release of said therapeutic material and prevent resorption back into the gum base, wherein said coating agent is gum arabic, a dextrin, gum tragacanth, gelatin, pectin, carboxymethyl cellulose, alginate, or other hydrocolloid or mixtures thereof, and a relatively water-insoluble phase consisting essentially of a plurality of separate and distinct masses suspended in and dispersed throughout the water-soluble phase, each of said masses comprising gum base, the water-soluble phase releasing said therapeutic material upon chewing.

2. The chewing gum as defined in claim 1 wherein said coating agent is gum arabic.

3. The chewing gum as defined in claim 1 wherein said coating agent is a dextrin, gum tragacanth, gelatin, pectin, carboxymethyl cellulose, alginate, or other hydrocolloid or mixtures thereof.

4. The chewing gum as defined in claim 1 wherein said coating agent is employed in a weight ratio of the therapeutic material of within the range of from about 1:

4 to about 1;

2.

5. The chewing gum as defined in claim 1 wherein said therapeutic material is dicalcium phosphate, magnesium hydroxide, calcium carbonate, aluminum hydroxide, nystatin, fat-soluble vitamins, antibiotics, propranolol, nadolol, or other medicaments.

6. The chewing gum as defined in claim 1 wherein said therapeutic material is dicalcium phosphate.

7. The chewing gum as defined in claim 1 wherein said therapeutic material is an antacid selected from the group consisting of magnesium hydroxide, calcium carbonate, aluminum hydroxide, magnesium carbonate and magnesium trisilicate.

8. The chewing gum as defined in claim 1 wherein said therapeutic material is an antibiotic selected from the group consisting of nystatin, amphotericin B and econazole.

9. The chewing gum as defined in claim 5 wherein said therapeutic material is propranolol or nadolol.

10. The chewing gum as defined in claim 1 further including a first sweetener in particulate form dispersed throughout the softener in said water soluble phase.

11. The chewing gum as defined in claim 10 wherein said first sweetener comprises a sugar, a sugar alcohol or mixtures thereof, and said second sweetener comprises a sugar or sugar alcohol or mixtures thereof.

12. The chewing gum as defined in claim 10, wherein said softener comprises sorbitol syrup, maltitol syrup, xylitol, corn syrup, hydrogenated starch hydrolysate or mixtures thereof.

13. The chewing gum as defined in claim 1 further including particles of a second sweetener enveloped by said gum base masses.

14. The chewing gum as defined in claim 13 wherein said second sweetener is sucrose, xylitol, mannitol, sorbitol, fructose syrup, glucose, glycyrrhizin, mono-ammonium salt of glycyrrhizin, calcium salt of glycyrrhizin, mono-, di- or trisodium salt of glycyrrhizin, mono-, di- or tripotassium salt of glycyrrhizin, calcium saccharin, sodium saccharin, ammonium saccharin, dihydrochalcones, neohesperidin dihydrochalcone, aspartame, Acesulfame-K, cyclamate salts, Stevia rebaudiana, Richardella dulcifica, Dioscoreophyllum cumminsii, and mixtures thereof.

15. The chewing gum as defined in claim 1 wherein said softener is sorbitol syrup.

16. The chewing gum as defined in claim 1 wherein said gum base is present in an amount within the range of from about 12 to about 25% by weight of the chewing gum.

17. The chewing gum as defined in claim 1 wherein said first sweetener is sorbitol powder, said softener is sorbitol syrup, and said second sweetener is mannitol, sorbitol or mixtures thereof.

18. The chewing gum as defined in claim 1 wherein said first sweetener is sucrose, said softener is sorbitol syrup and said second sweetener is sucrose.

19. The chewing gum as defined in claim 1 wherein said chewing gum is a sugarless gum and said water-soluble phase comprises from about 50 to about 92% by weight of the chewing gum, and said water-insoluble phase comprises from about 8 to about 50% by weight of the chewing gum.

20. A method for forming a chewing gum as defined in claim 1 which comprises interdispersing in melted gum base particles of a second sweetener to form a continuous phase, and thereafter mixing the continuous phase with a first sweetener causing the continuous phase to be torn into discrete masses of gum base enveloping said particles of second sweetener, mixing aqueous softener with the mixture of said discrete masses and first sweetener, and mixing said therapeutic material with said mixture of aqueous softener, said discrete masses and first sweetener to form a chewing gum which is smooth and continuous.

21. The method as defined in claim 20 wherein said therapeutic material is coated with gum arabic.

22. The chewing gum as defined in claim 1 having a short nougat-like discontinuous structure which is easily torn apart.