IP Library Granted Patent US 11,147,850
Granted Patent B2
US 11,147,850 · App. 15/518,107 · Granted Oct 19, 2021

Synergistic composition for osteoarthritis

Inventors: Ganga Raju Gokaraju (Vijayawada, IN); Rama Raju Gokaraju (Vijayawada, IN); Venkata Kanaka Ranga Raju Gokaraju (Vijayawada, IN); Trimurtulu Golakoti (Vijayawada, IN); Kiran Bhupathiraju (Vijayawada, IN)
Assignee: Laila Nutraceuticals
A61K36/9066A61K9/0014A61K9/0053A61K31/353A61K31/715A61K36/48A61K2236/33
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Quick Facts
Patent No.
US 11,147,850
App. No.
15/518,107
Granted
Oct 19, 2021
Kind
B2
Abstract

The present invention relates to synergistic compositions for the treatment of one or more associated conditions of arthritis or rheumatoid arthritis osteoarthritis. More particularly, novel synergistic compositions which comprises a combination of therapeutically effective amounts of: a) an alcoholic/hydroalcoholic extract of Tamarindus indica seed comprising proanthocyanidins either alone or in combination with water extract of Tamarindus indica seed comprising polysaccharides, b) a Curcuma longa rhizome extract comprising curcuminoids, c) optionally containing pharmaceutically or nutraceutically or dietetically acceptable carriers/excipients. The invention also relates to a method of treating one or more associated conditions of arthritis or rheumatoid arthritis or osteoarthritis using synergistic composition.

Claims (36)

1. A dosage form comprising:

a combination of therapeutically effective amounts of:

a) A Tamarindus indica seed extract comprising:

an alcohol or hydroalcohol extract of a Tamarindus indica seed, wherein the alcohol or hydroalcohol extract comprises proanthocyanidins; and

a water extract of a Tamarindus indica seed, the water extract comprising polysaccharides;

wherein the alcohol or hydroalcohol extract of the Tamarindus indica seed and the water extract of the Tamarindus indica seed are used in a ratio ranging from 1:1 to 10:1; and

b) A Curcuma longa rhizome extract comprising curcuminoids,

wherein the Tamarindus indica seed extract and the Curcuma longa rhizome extract are used in a ratio ranging from 1:3 to 3:1; and

a pharmaceutically, nutraceutically, or dietetically acceptable excipient or carrier.

2. A composition comprising a combination of:

a) a Tamarindus indica seed extract comprising:

an alcohol or hydroalcohol extract of a Tamarindus indica seed, the alcohol or hydroalcohol extract comprising proanthocyanidins; and

a water extract of a Tamarindus indica seed, the water extract comprising polysaccharides; and

b) a Curcuma longa rhizome extract comprising curcuminoids, wherein:

the combination is present in an amount which is effective for the treatment of inflammation,

the Tamarindus indica seed extract and the Curcuma longa rhizome extract are used in a ratio ranging from 1:3 to 3:1, and

the Tamarindus indica seed extract comprises:

from 50% to 91% by weight of an alcohol or hydroalcohol extract of a Tamarindus indica seed, the alcohol or hydroalcohol extract comprising proanthocyanidins; and

from 9% to 50% of a water extract of a Tamarindus indica seed, the water extract comprising predominantly polysaccharides.

3. The composition according to claim 2 , wherein the alcohol used for preparing the alcohol or hydroalcohol extract of the Tamarindus indica seed is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, tert-butanol, and mixtures thereof.

4. The composition according to claim 2 , wherein the Curcuma longa rhizome extract is prepared from a Curcuma longa rhizome using a solvent selected from the group consisting of methanol, ethanol, propanol, isopropanol, n-butanol, tert-butanol, acetone, ethyl acetate, and mixtures thereof.

5. The composition according to claim 2 , further comprising a pharmaceutically, nutraceutically, or dietetically acceptable carrier or excipient.

6. The composition according to claim 5 , wherein the pharmaceutically, nutraceutically, or dietetically acceptable carrier or excipient is selected from the group consisting of surfactants, binders, diluents, disintegrants, lubricants, preservatives, stabilizers, buffers, polymers, colors, flavors, suspensions and drug delivery systems.

7. The dosage form according to claim 1 , wherein the combination comprises from greater than 0% to 30% of the excipient or carrier.

8. The dosage form according to claim 1 , wherein the combination comprises:

from 40% to 70% of the Tamarindus indica seed extract; and

from greater than 0% to 15% of the excipient or carrier.

9. The dosage form according to claim 1 , wherein the combination comprises:

a) 60% of the Tamarindus indica seed extract;

b) 30% of the Curcuma longa rhizome extract comprising curcuminoids; and

c) 10% the excipient or carrier.

10. The composition according to claim 2 , wherein the composition is formulated to be administered orally or topically.

11. A method for treating at least one disease condition selected from the group consisting of inflammation, arthritis, joint pain, rheumatoid arthritis, osteoarthritis, chronic non-rheumatoid arthritis, and collagen degradation in a patient in need thereof, comprising administering to the patient an effective amount of the composition as claimed in claim 2 .

12. A method for treating at least one disease condition selected from the group consisting of inflammation, arthritis, joint pain, rheumatoid arthritis, osteoarthritis, chronic non-rheumatoid arthritis, and collagen degradation in a patient in need thereof, comprising administering to the patient an effective amount of the dosage form according to claim 9 .

13. The composition according to claim 2 , wherein the composition is useful for the prevention or treatment of at least one condition selected from inflammation, arthritis, joint pain, rheumatoid arthritis, osteoarthritis, chronic non-rheumatoid arthritis, collagen degradation.

14. A method for treating at least one disease condition selected from the group consisting of inflammation, arthritis, joint pain, rheumatoid arthritis, osteoarthritis, chronic non-rheumatoid arthritis, and collagen degradation in a patient in need thereof, comprising administering to the patient an effective amount of the dosage form as claimed in claim 7 .

Assignments (2)
CHANGE OF NAME Recorded Aug 18, 2025
From: LAILA NUTRACEUTICALS
To: LAILA NUTRA PRIVATE LIMITED
Reel/Frame 072508/0229 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2017
From: GOKARAJU, GANGA RAJU; GOKARAJU, RAMA RAJU; GOKARAJU, VENKATA KANAKA RANGA RAJU; GOLAKATI, TRIMURTULU; BHUPATHIRAJU, KIRAN
To: LAILA NUTRACEUTICALS
Reel/Frame 042709/0917 →
Priority Claims (1)
IN 5106/CHE/2014 · Oct 10, 2014 · national
Continuity (1)
Related Publication 20170290875A1 · Oct 12, 2017