Orally administrable solid pharmaceutical composition and a process thereof

Patent metadata

Field	Value
Publication number	US-9241908-B2
Application number	US-68282508-A
Country	US
Kind code	B2
Filing date	Oct 16, 2008
Priority date	Oct 16, 2007
Publication date	Jan 26, 2016
Grant date	Jan 26, 2016

Abstract

The invention relates to improvised pharmaceutical compositions permitting ingestion via oral delivery of proteins/peptides or their conjugates, and/or cation-insulin conjugate complexes demonstrating desirable pharmacokinetic profiles and potency in efficacy models of diabetes in dogs and humans. A preferred formulation comprises 0.01%-20% w/w of insulin, insulin compound conjugates and/or cation insulin conjugates, 10%-60% w/w of one or more fatty acid components selected from saturated or unsaturated C4-C12 fatty acids and/or salts of such fatty acids and additionally contains optimal amounts of other pharmaceutically suitable polymer excipients which permit improved solubility, dissolution rate and effective bioavailability of poorly water soluble compositions and consistent in-vivo release profiles upon scalability during manufacture. A further aspect of the invention features the process of preparing the aforesaid formulations.

First claim

We claim:

1. An orally administrable tablet pharmaceutical composition of IN-105 comprising about 0.01%-20% w/w of IN-105 which is an insulin compound conjugate, about 10%-60% w/w of saturated or unsaturated C 4 -C 12 fatty acids, fatty acid esters or salts thereof, 10%-60% w/w of a diluent, 1%-20% w/w of disintegrant, 0.5% w/w of a lubricant and optionally including binders, plasticizers, permeation enhancers and solubilizers, wherein the lubricant is magnesium stearate.

2. The pharmaceutical composition of claim 1 , wherein the fatty acid component is capric acid and/or lauric acid or salts thereof.

3. The pharmaceutical composition of claim 1 , wherein the binder is selected from the group consisting of polyvinylpyrrolidone, carboxymethylcellulose, methylcellulose, starch, gelatin, sugars, natural gums, synthetic gums and combinations thereof.

4. The pharmaceutical composition of claim 1 , wherein the diluents is selected from the group consisting of calcium salts, cellulose, cellulose derivatives, palatinose, organic acids, sugar, sugar alcohols, pectate salts and combinations thereof.

5. The pharmaceutical composition of claim 1 , wherein the disintegrant is selected from the group consisting of cross-linked polyvinylpyrrolidone, carboxymethylcellulose, methyl cellulose, cation-exchange resins, alginic acid, guar gum and their combinations thereof.

6. The pharmaceutical composition of claim 1 , wherein the permeation enhancer is selected from the group consisting of sodium lauryl sulfate, sodium laurate, palmitoyl carnitine, phosphatidylcholine, cyclodextrin, cyclodextrin derivatives, carnithine, carnithine derivatives, mucoadhesive polymers, zonula occludins toxin, bile salts, fatty acids and combinations thereof.

7. The pharmaceutical composition of claim 1 , wherein the plasticizer is selected from the group consisting of polyethyleneglycol, propylene glycol, acetyl citrate, triacetin, acetylated monoglyceride, rape oil, olive oil, sesame oil, acetyltriethyl citrate, glycerin sorbitol, diethyloxalate, diethylmalate, diethylfumarate, dibutylsuccinate, dibutyl phthalate, dioctylphthalate, dibutylsebacate, triethylcitrate, tributylcitrate, glyceroltributyrate, glyceryl triacetate and mixtures thereof.

8. A process for manufacturing an orally administrable solid pharmaceutical composition of IN 105, comprising about 0.01%-20% w/w of IN-105, about 10%-60% w/w of saturated or unsaturated C4-C12 fatty acids, fatty acid esters or salts thereof, 10%-60% w/w of a diluent, 1%-20% w/w of disintegrant, 0.5% w/w of a lubricant and optionally including binders, plasticizers, permeation enhancers and solubilizers, wherein the lubricant is magnesium stearate, the method comprising the steps of:
a. grinding a suitable saturated or unsaturated C4-C12 fatty acids and/or salts of such fatty acid;
b. granulating the resulting fatty acid obtained from step (a) with an organic solvent;
c. air-drying the granules obtained from step (b);
d. rasping the dried granules through a mesh to obtain granules of desired particle size;
e. blending the fatty acid granules with the cation-insulin conjugate complex with the other excipients; and
f. compressing the blended mixture for tablet formation.

9. A process for manufacturing an orally administrable tablet pharmaceutical composition of IN105, comprising about 0.01%-20% w/w of IN-105, about 10%-60% w/w of saturated or unsaturated C4-C12 fatty acids, fatty acid esters or salts thereof, 0.01%-5% of binder, 10%-60% w/w of a diluent, 1%-20% w/w of disintegrant, 0.5% w/w of a lubricant and optionally including binders, plasticizers, permeation enhancers and solubilizers, wherein the lubricant is magnesium stearate, the method comprising the steps of:
a. grinding suitable saturated or unsaturated C4-C12 fatty acids and/or salts of such fatty acid and a binder;
b. suspending the cation-insulin conjugate complex in an organic solvent using the binder to form a wet mass;
c. granulation of the components obtained from step (b) using the binder to form dried granules;
d. rasping the dried granules of step (c);
e. blending the dried granules with other excipients; and
f. compressing the blended mixture for tablet formation.

10. A process according to claim 8 or 9 , wherein the organic solvent used is selected from the group comprising isopropanol, acetone, methyl alcohol, methyl isobutyl ketone, chloroform, 1-propanol, 2-propanol, acetonitrile, 1-butanol, 2-butanol, ethyl alcohol, cyclohexane, dioxane, ethyl acetate, dimethylformamide, dichloroethane, hexane, isooctane, methylene chloride, tert-butyl alcohol, toluene, carbon tetrachloride, or combinations thereof.

11. A 5-500 mg tablet of an orally administrable tablet pharmaceutical composition according to claim 1 .

12. A tablet according to claim 11 , being a 50 mg tablet, a 100 mg tablet, a 150 mg tablet, a 200 mg tablet or a 250 mg tablet.

13. A dose of the orally administrable tablet pharmaceutical composition of claim 1 , to achieve a maximum control of post prandial blood glucose concentration in diabetic patients within 5-60 minutes post-administration.

14. The orally administrable tablet pharmaceutical composition according to claim 1 , which produces a lowered serum glucose in human patients by at least 5% within 120 minutes post oral administration.

15. A stable orally administrable tablet pharmaceutical composition of IN-105 according to claim 1 , characterized in that said composition remains stable over exposure to conditions selected from the group consisting of
a. temperature range of about 2-40° C.; and
b. 25° C.±2° C./60%±5% relative humidity (RH), 30° C.±2° C./65%±5% relative humidity, 40° C.±2° C./75%±5% relative humidity for over a period of at least 6 months.

16. The stable orally administrable tablet pharmaceutical composition according to claim 15 , characterized in that impurities do not increase by more than 5% when compared to the impurity levels at the time of manufacture.

17. The stable orally administrable tablet pharmaceutical composition according to claim 15 , characterized in that impurities do not increase by more than 10% when compared to the impurity levels at the time of manufacture.

18. The stable orally administrable tablet pharmaceutical composition according to claim 15 , characterized in that an assay of said compound in the composition does not decrease by more than 10%.

19. The stable orally administrable tablet pharmaceutical composition according to claim 1 , characterized in that a dissolution profile is at least 75% at any said time interval.

20. The stable orally administrable tablet pharmaceutical composition according to claim 19 , wherein a time interval ranges for a period over 2 years.

21. The stable orally administrable tablet pharmaceutical composition according to claim 15 , characterized in that a difference between a hardness profile is no more than 1 kg/cm 2 when compared to a hardness profile at the time of manufacture.

22. The stable orally administrable tablet pharmaceutical composition according to claim 15 , characterized in that at least 95%±2% of the composition remains undegraded over exposure to conditions selected from the group consisting of:
(a) temperature range of about 2-8° C. or 25° C.-40° C.; and
(b) 25° C.±2° C./60%±5% relative humidity (RH), 30° C.±2° C./65%±5% relative humidity, 40° C.±2° C./75%±5% relative humidity for over a period of at least 6 months.

23. The stable orally administrable tablet phar

Assignees

• Khedkar Anand
• Rangappa Sharath Kumar Mallapura
• Subramani Ramesh
• Dave Nitesh
• Radhakrishnan Devesh
• Shankar Sundaresh
• Chivukula Sudheer
• Ramakrishna Ranjith
• Murthy Shanmugam Thandava
• Pai Harish Venkatraman
• Sengupta Nilanjan
• Melarkode Ramakrishnan
• Iyer Harish
• Biocon Ltd

Inventors

• Khedkar Anand
• Rangappa Sharath Kumar Mallapura
• Subramani Ramesh
• Dave Nitesh
• Radhakrishnan Devesh
• Shankar Sundaresh
• Chivukula Sudheer
• Ramakrishna Ranjith
• Murthy Shanmugam Thandava
• Pai Harish Venkatraman
• Sengupta Nilanjan
• Melarkode Ramakrishnan
• Iyer Harish

Classifications

• A61K47/14

  Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters · CPC title

• A61K38/28

  Insulins · CPC title

• A61K9/2018

  Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates · CPC title

• A61K9/2013 Primary

  Organic compounds, e.g. phospholipids, fats · CPC title

• A61K9/20 Primary

  Pills, tablets, {discs, rods (A61K9/0004, A61K9/0007, A61K9/0056, A61K9/0065 take precedence; for reconstitution of a drink A61K9/0095)} · CPC title