IP Library Patent Application 12998655
Patent Application
App. No. 12/998,655

DIRECTLY COMPRESSIBLE HIGH FUNCTIONALITY GRANULAR DIBASIC CALCIUM PHOSPHATE BASED CO-PROCESSED EXCIPIENT

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Quick Facts
Patent No.
US None
App. No.
12/998,655
Abstract

An improved excipient comprising substantially homogeneous particles of a compressible, high functionality granular dibasic calcium phosphate based excipient is provided. The improved excipient comprises dibasic calcium phosphate, a binder and a disintegrant, and is formed by spraying a homogeneous slurry of the components. The improved excipient provides enhanced flowability/good flow properties, an increased API loading and blendability and higher compactibility as compared to the individual components, and as compared to excipients formed from the same materials by conventional methods. The improved excipient has strong intraparticle bonding bridges between the components, resulting in a unique structural morphology including significant open structures or hollow pores. The presence of these pores provides a surface roughness that is the ideal environment for improved blending with an API.

Claims (94)

1 . A composition comprising:

about 75% to about 98% dibasic calcium phosphate;

about 1% to about 10% at least one binder; and

about 1% to about 20% at least one disintegrant,

wherein the dibasic calcium phosphate, binder and disintegrant form substantially homogeneous spherical particles in which the dibasic calcium phosphate, binder and disintegrant are indistinguishable when viewed with a SEM.

2 . The composition of claim 1 wherein the composition includes:

about 80% to about 90% dibasic calcium phosphate;

about 2% to about 8% at least one binder; and

about 3% to about 12% at least one disintegrant.

3 . The composition of claim 1 wherein the composition includes:

about 85% to about 93% dibasic calcium phosphate;

about 2% to about 5% at least one binder; and

about 10% at least one disintegrant.

4 . The composition of claim 1 wherein the binder includes hydroxypropyl methylcellulose and the disintegrant includes cross-linked polyvinylpyrrolidone.

5 . The composition of claim 1 wherein the excipient is formed by spraying an aqueous slurry comprised of the dibasic calcium phosphate, binder and disintegrant.

6 . A method of making an excipient comprising:

forming a dibasic calcium phosphate slurry;

forming a binder slurry;

forming a disintegrant slurry;

homogenizing the dibasic calcium phosphate slurry and the disintegrant slurry to form a DCP/disintegrant slurry;

adding the binder slurry to the DCP/disintegrant slurry;

and spray dry granulating the final slurry to form particles of excipient,

wherein the dibasic calcium phosphate, binder and disintegrant are indistinguishable when viewed with a SEM, thereby forming substantially homogeneous spherical particles.

7 . The method of claim 6 wherein:

about 75% to about 98% dibasic calcium phosphate;

about 1% to about 10% at least one binder; and

about 1% to about 20% at least one disintegrant.

8 . The method of claim 6 comprising:

about 80% to about 90% dibasic calcium phosphate;

about 2% to about 8% at least one binder; and

about 3% to about 12% at least one disintegrant.

9 . The method of claim 6 comprising:

about 85% to about 93% dibasic calcium phosphate;

about 2% to about 5% at least one binder; and

about 10% at least one disintegrant.

10 . The method of claim 6 wherein the binder includes hydroxypropyl methylcellulose and the disintegrant includes cross-linked polyvinylpyrrolidone.

11 . A method of making an excipient comprising:

forming a dibasic calcium phosphate slurry;

forming a hydroxypropyl methylcellulose slurry;

forming a cross-linked polyvinylpyrrolidone slurry;

homogenizing the dibasic calcium phosphate slurry and the cross-linked polyvinylpyrrolidone slurry to form a DCP/cross-linked polyvinylpyrollidone slurry;

adding the hydroxypropyl methylcellulose slurry to the DCP/cross-linked polyvinylpyrollidone slurry; and

spray dry granulating the final slurry to form particles of excipient,

wherein the dibasic calcium phosphate, hydroxypropyl methylcellulose and cross-linked polyvinylpyrrolidone are indistinguishable when viewed with a SEM, thereby forming substantially homogeneous spherical particles.

12 . The method of claim 11 comprising:

about 75% to about 98% dibasic calcium phosphate;

about 1% to about 10% hydroxypropyl methylcellulose; and

about 1% to about 20% at least one cross-linked polyvinylpyrrolidone.

13 . The method of claim 11 comprising:

about 80% to about 90% dibasic calcium phosphate;

about 2% to about 8% hydroxypropyl methylcellulose; and

about 3% to about 12% at least one cross-linked polyvinylpyrrolidone.

14 . The method of claim 11 comprising:

about 85% to about 93% dibasic calcium phosphate;

about 2% to about 5% hydroxypropyl methylcellulose; and

about 10% at least one cross-linked polyvinylpyrrolidone.

15 . A pharmaceutical tablet comprising:

at least one active pharmaceutical ingredient; and

an excipient of substantially homogeneous particles including:

a) dibasic calcium phosphate;

b) at least one binder; and

c) at least one disintegrant.

16 . The tablet of claim 15 wherein the excipient includes:

about 75% to about 98% dibasic calcium phosphate;

about 1% to about 10% at least one binder; and

about 1% to about 20% at least one disintegrant.

17 . The tablet of claim 15 wherein the excipient includes:

about 80% to about 90% dibasic calcium phosphate;

about 2% to about 8% at least one binder; and

about 3% to about 12% at least one disintegrant.

18 . The tablet of claim 15 wherein the excipient includes:

about 85% to about 93% dibasic calcium phosphate;

about 2% to about 5% at least one binder; and

about 10% at least one disintegrant.

19 . The tablet of claim 15 wherein the binder includes hydroxypropyl methylcellulose and the disintegrant includes cross-linked polyvinylpyrrolidone.

20 . A method of making a pharmaceutical tablet comprising:

mixing at least one active pharmaceutical ingredient with an excipient of substantially homogeneous particles including:

a) dibasic calcium phosphate;

b) at least one binder; and

c) at least one disintegrant to form a mixture; and

compressing the mixture to form a tablet.

21 . The method of claim 20 wherein the excipient includes:

about 75 to about 98% dibasic calcium phosphate;

about 1% to about 10% at least one binder; and

about 1% to about 20% at least one disintegrant.

22 . The method of claim 20 wherein the excipient includes:

about 80% to about 90% dibasic calcium phosphate;

about 2% to about 8% at least one binder; and

about 3% to about 12% at least one disintegrant.

23 . The method of claim 20 wherein the excipient includes:

about 85% to about 93% dibasic calcium phosphate;

about 2% to about 5% at least one binder; and

about 10% at least one disintegrant.

24 . The method of claim 20 wherein the binder includes hydroxypropyl methylcellulose and the disintegrant includes cross-linked polyvinylpyrrolidone.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jun 21, 2016
From: CREDIT SUISSE, AG, CAYMAN ISLANDS BRANCH
To: AVANTOR PERFORMANCE MATERIALS, INC.
Reel/Frame 039111/0908 →
PATENT SECURITY AGREEMENT Recorded Jun 24, 2011
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 026499/0256 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2011
From: DEORKAR, NANDU; FARINA, JAMES; MIINEA, LILIANA; RANDIVE, SAMEER
To: AVANTOR PERFORMANCE MATERIALS, INC
Reel/Frame 026376/0160 →