IP Library Granted Patent US 7,687,075
Granted Patent B2
US 7,687,075 · App. 10/988,693 · Granted Mar 30, 2010

Colonic purgative composition with soluble binding agent

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Quick Facts
Patent No.
US 7,687,075
App. No.
10/988,693
Granted
Mar 30, 2010
Kind
B2
Abstract

This invention relates to novel colonic purgative compositions in a solid dosage form, comprising at least one purgative and at least one soluble, or soluble, nonfermentable binder, such as polyethylene glycol. Further, this invention relates to methods of using the colonic purgative compositions. The present compositions and methods are designed to improve patient tolerance and compliance, while at the same time improving the quality of bowel cleansing. The formulations and methods of this invention are particularly useful to cleanse the bowel prior to diagnostic and surgical procedures and can also be employed in lower dosages as a laxative to promote elimination and/or to relieve constipation.

Claims (61)

1. A colonic purgative formulation in a solid dosage tablet form comprising:

(a) sodium phosphate; and

(b) between 7.5% and 15% of polyethylene glycol by weight, wherein the polyethylene glycol has an average molecular weight of 7,000 to 9,000 daltons and is uniformly distributed in the tablet so that the polyethylene glycol binds the sodium phosphate together to maintain the tablet form, and wherein a dosage of the formulation comprises 42-60 grams of sodium phosphate, and wherein the tablet form is for oral administration.

2. The formulation of claim 1 , wherein the sodium phosphate comprises monobasic sodium phosphate, dibasic sodium phosphate, or a combination thereof.

3. The formulation of claim 1 , wherein the tablet comprises a lubricant.

4. The formulation of claim 3 , wherein the lubricant comprises magnesium stearate.

5. A colonic purgative formulation in tablet form comprising:

(a) sodium phosphate monobasic from 45 to 75% by weight;

(b) sodium phosphate dibasic from 15 to 30% by weight;

(c) polyethylene glycol 8,000 from 5 to 20% by weight, wherein the polyethylene glycol provides a matrix upon which the sodium phosphate monobasic and sodium phosphate dibasic associate together to maintain the tablet form; and

(d) magnesium stearate from 0.10 to 1.50% by weight, and wherein all of the weights are based on the total weight of the formulation.

6. A colonic purgative formulation in tablet form, comprising:

(a) sodium phosphate from 15 to 90% by weight;

(b) polyethylene glycol 8,000 from 5 to 20% by weight, wherein the polyethylene glycol provides a matrix upon which the sodium phosphate associates to maintain the tablet form; and

(c) magnesium stearate from 0.10 to 1.50% by weight, and wherein all of the weights are based on the total weight of the formulation.

7. A kit comprising a colonic purgative formulation in tablet form for oral administration, wherein each tablet comprises:

(a) at least one soluble binder comprising 5 to 20% polyethylene glycol, wherein the polyethylene glycol has an average molecular weight of 7,000 to 9,000 daltons; and

(b) about 1.5 grams of sodium phosphate wherein the polyethylene glycol is distributed throughout the tablet so that the polyethylene glycol binds the sodium phosphate together to maintain the tablet form.

8. The formulation of claim 1 , wherein the polyethylene glycol has an average molecular weight of 8,000.

9. The formulation of claim 1 , wherein the polyethylene glycol comprises 10% by weight of the formulation.

10. The formulation of claim 1 , wherein the tablet disintegrates within about 11 minutes.

11. The formulation of claim 1 , wherein the formulation comprises 48 g of sodium phosphate divided between 32 tablets.

12. The formulation of claim 11 , wherein the dosage comprises 20 tablets of the formulation being taken as 4 tablets at a time with 8 ounces of clear liquid every 15 minutes an evening before a colonoscopy.

13. The formulation of claim 11 , wherein the dosage comprises 12 tablets of the formulation being taken as 4 tablets at a time with 8 ounces of clear liquid beginning 3 to 5 hours before a colonoscopy.

14. The formulation of claim 1 , wherein mean increase from baseline of inorganic phosphorus levels occurs after administration of the formulation.

15. The formulation of claim 1 , wherein the dosage produces mild catharsis.

16. A colonic purgative formulation in tablet form for oral administration wherein each tablet comprises 7.5% to 15% polyethylene glycol as a binder and about 1.5 grams of sodium phosphate, wherein the polyethylene glycol is admixed with the sodium phosphate in the tablet so that the polyethylene glycol binds the sodium phosphate together to maintain the tablet form and wherein the polyethylene glycol has an average molecular weight of 7,000 to 9,000 daltons.

17. The formulation of claim 16 , wherein the tablet comprises about 1100 milligrams of sodium phosphate monobasic.

18. The formulation of claim 16 , wherein the tablet comprises about 398 milligrams of sodium phosphate dibasic.

19. The formulation of claim 16 , wherein the tablet comprises magnesium stearate.

20. The formulation of claim 16 , wherein the tablet comprises about 8.4 milligrams of magnesium stearate.

21. The formulation of claim 16 , wherein the tablet has a mass of about 1676 milligrams.

22. The formulation of claim 16 , wherein the polyethylene glycol is polyethylene glycol 8000.

23. The formulation of claim 22 , wherein the formulation comprises about 10% w/w of polyethylene glycol 8000.

24. A formulation in tablet form for oral administration, wherein each tablet comprises about 167 milligrams of polyethylene glycol having an average molecular weight between 7000 and 9000 daltons, about 1100 milligrams of sodium phosphate monobasic and about 398 milligrams of sodium phosphate dibasic.

25. The formulation of claim 24 , wherein the polyethylene glycol is polyethylene glycol 8000.

26. The formulation of claim 24 , further comprising magnesium stearate.

27. A purgative for cleansing a colon prior to a colonoscopy, the purgative comprising 48 grams of sodium phosphate in tablet form, wherein each tablet comprises about 1.5 grams of sodium phosphate and wherein the tablet also comprises 7.5% to 15% polyethylene glycol 8000, and wherein the polyethylene glycol is admixed with the sodium phosphate in the tablet so that the polyethylene glycol binds the sodium phosphate together to maintain the tablet form.

28. The purgative of claim 27 , wherein each tablet comprises about 1102 milligrams of sodium phosphate monobasic and about 398 milligrams of sodium phosphate dibasic.

29. The purgative of claim 27 , wherein each tablet comprises magnesium stearate.

30. The purgative of claim 27 , wherein a dosage of the purgative comprises four tablets taken every 15 minutes.

31. A colonic purgative formulation in tablet form for oral administration, comprising sodium phosphate and polyethylene glycol, wherein the polyethylene glycol has an average molecular weight between 7000 and 9000 daltons and is distributed in the tablet so that the polyethylene glycol binds the sodium phosphate together to maintain the tablet form, the tablet made by a method comprising:

heating a mixture comprising the sodium phosphate and the polyethylene glycol to the melting point of the polyethylene glycol; and

compressing the formulation into a tablet.

32. The colonic purgative formulation of claim 31 , wherein the polyethylene glycol is polyethylene glycol 8000.

33. The colonic purgative formulation of claim 31 , wherein the mixture is allowed to cool down prior to compressing the formulation into a tablet.

34. The colonic purgative formulation of claim 33 , wherein the mixture is allowed to cool down overnight prior to compressing the formulation into a tablet.

35. The formulation of claim 5 , wherein the tablet disintegrates within about 11 minutes.

36. The formulation of claim 6 , wherein the tablet disintegrates within about 11 minutes.

37. The formulation of claim 16 , wherein the tablet disintegrates within about 11 minutes.

38. The formulation of claim 24 , wherein the tablet disintegrates within about 11 minutes.

39. The formulation of claim 5 , wherein the formulation comprises 32 tablets.

40. The formulation of claim 5 , wherein the formulation comprises 40 tablets.

41. The formulation of claim 6 , wherein the formulation comprises 32 tablets.

42. The formulation of claim 6 , wherein the formulation comprises 40 tablets.

43. The formulation of claim 16 , wherein the formulation comprises 32 tablets.

44. The formulation of claim 16 , wherein the formulation comprises 40 tablets.

45. The purgative of claim 27 , wherein the tablet comprises about 10% w/w of polyethylene glycol 8000.

46. The purgative of claim 27 , wherein a dosage of the purgative comprises four tablets taken every 15 minutes for a total of 20 tablets the evening before a colonoscopy procedure.

47. The purgative of claim 27 , wherein a dosage of the purgative comprises four tablets taken every 15 minutes for a total of 12 tablets the day of a colonoscopy procedure.

48. The formulation of claim 16 wherein the tablet binder consists essentially of polyethylene glycol.

Assignments (18)
RELEASE OF SECURITY INTEREST Recorded Nov 20, 2025
From: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
To: ATON PHARMA, INC.; BAUSCH & LOMB INCORPORATED; BAUSCH & LOMB PHARMA HOLDINGS CORP.; COMMONWEALTH LABORATORIES, LLC; DOW PHARMACEUTICAL SCIENCES, INC.; ECR PHARMACEUTICALS CO., INC.; LABORATOIRE CHAUVIN S.A.S.; MEDICIS PHARMACEUTICAL CORPORATION; ONPHARMA INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, LTD.; SALIX PHARMACEUTICALS, INC.; SANTARUS, INC.; SOLTA MEDICAL, INC.; SYNERGETICS USA, INC.; TECHNOLAS PERFECT VISION GMBH; VALEANT CANADA LP; VALEANT PHARMACEUTICALS INTERNATIONAL; VALEANT PHARMACEUTICALS INTERNATIONAL, INC.; VALEANT PHARMACEUTICALS NORTH AMERICA LLC; WIRRA IP PTY LIMITED; VALEANT PHARMA POLAND SP. Z O.O.; VALEANT PHARMACEUTICALS LUXEMBOURG S.A R.L.; VALEANT PHARMACEUTICALS IRELAND LIMITED
Reel/Frame 073637/0001 →
RELEASE OF SECURITY INTEREST Recorded Nov 20, 2025
From: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
To: BAUSCH HEALTH AMERICAS, INC.; BAUSCH & LOMB INCORPORATED; BAUSCH HEALTH US, LLC; SOLTA MEDICAL, INC.; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.
Reel/Frame 073637/0126 →
RELEASE OF SECURITY INTEREST Recorded Nov 20, 2025
From: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
To: BAUSCH & LOMB INCORPORATED; BAUSCH HEALTH US, LLC; SOLTA MEDICAL, INC.; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH AMERICAS, INC.
Reel/Frame 073654/0242 →
U.S. PATENT SECURITY AGREEMENT Recorded Jun 13, 2025
From: MEDICIS PHARMACEUTICAL CORPORATION; ORAPHARMA, INC.; BAUSCH HEALTH US, LLC (F/K/A VALEANT PHARMACEUTICALS NORTH AMERICA LLC); PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, INC.; SANTARUS, INC.; BAUSCH HEALTH AMERICAS, INC.; SOLTA MEDICAL, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071566/0200 →
U.S. PATENT SECURITY AGREEMENT Recorded Jun 13, 2025
From: MEDICIS PHARMACEUTICAL CORPORATION; ORAPHARMA, INC.; BAUSCH HEALTH US, LLC (F/K/A VALEANT PHARMACEUTICALS NORTH AMERICA LLC); PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, INC.; SANTARUS, INC.; BAUSCH HEALTH AMERICAS, INC.; SOLTA MEDICAL, INC.
To: THE BANK OF NEW YORK MELLON
Reel/Frame 071564/0463 →
RELEASE OF SECURITY INTEREST Recorded Apr 8, 2025
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: SOLTA MEDICAL, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH IRELAND LIMITED (F/K/A/ VALEANT PHARMACEUTICALS IRELAND LIMITED); SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; HUMAX PHARMACEUTICAL S.A.; SOLTA MEDICAL IRELAND LIMITED; BAUSCH & LOMB MEXICO, S.A. DE C.V.; BAUSCH+LOMB OPS B.V.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH COMPANIES INC.; BAUSCH HEALTH HOLDCO LIMITED; BAUSCH HEALTH MAGYARORSZAG KFT (A/K/A BAUSCH HEALTH HUNGARY LLC); BAUSCH HEALTH POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (F/K/A VALEANT PHARMA POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA); BAUSCH HEALTH US, LLC; BAUSCH HEALTH, CANADA INC. / SANTE BAUSCH, CANADA INC.; ICN POLFA RZESZOW SPOLKA AKCYJNA (A/K/A ICN POLFA RZESZOW S.A.); ORAPHARMA, INC.; PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA SPOLKA AKCYJNA (A/K/A PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA S.A.); SOLTA MEDICAL DUTCH HOLDINGS B.V.; V-BAC HOLDING CORP.; VRX HOLDCO LLC; 1261229 B.C. LTD.; 1530065 B.C. LTD.
Reel/Frame 070778/0199 →
SECURITY AGREEMENT (SECOND LIEN) Recorded Oct 5, 2022
From: BAUSCH HEALTH US, LLC; BAUSCH HEALTH AMERICAS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; SOLTA MEDICAL, INC.
To: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
Reel/Frame 061606/0468 →
SECURITY AGREEMENT (FIRST LIEN) Recorded Oct 4, 2022
From: BAUSCH HEALTH US, LLC; BAUSCH HEALTH AMERICAS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; SOLTA MEDICAL, INC.
To: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
Reel/Frame 061595/0066 →
SECURITY AGREEMENT Recorded Feb 10, 2022
From: BAUSCH & LOMB INCORPORATED; BAUSCH HEALTH US, LLC; SOLTA MEDICAL, INC.; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH AMERICAS, INC.
To: THE BANK OF NEW YORK MELLON
Reel/Frame 059121/0001 →
SECURITY INTEREST Recorded Jun 8, 2021
From: BAUSCH & LOMB INCORPORATED; BAUSCH HEALTH US, LLC; SOLTA MEDICAL, INC.; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH AMERICAS, INC.
To: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
Reel/Frame 056811/0814 →
SECURITY INTEREST Recorded Mar 11, 2019
From: BAUSCH HEALTH AMERICAS, INC.; BAUSCH & LOMB INCORPORATED; BAUSCH HEALTH US, LLC; SOLTA MEDICAL, INC.; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.
To: THE BANK OF NEW YORK MELLON, AS NOTES COLLATERAL AGENT
Reel/Frame 048556/0758 →
SECURITY INTEREST Recorded Feb 26, 2018
From: ATON PHARMA, INC.; BAUSCH & LOMB INCORPORATED; BAUSCH & LOMB PHARMA HOLDINGS CORP.; COMMONWEALTH LABORATORIES, LLC; DOW PHARMACEUTICAL SCIENCES, INC.; ECR PHARMACEUTICALS CO., INC.; LABORATOIRE CHAUVIN S.A.S.; MEDICIS PHARMACEUTICAL CORPORATION; ONPHARMA INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, LTD.; SALIX PHARMACEUTICALS, INC.; SANTARUS, INC.; SOLTA MEDICAL, INC.; SYNERGETICS USA, INC.; TECHNOLAS PERFECT VISION GMBH; VALEANT CANADA LP; VALEANT PHARMACEUTICALS INTERNATIONAL; VALEANT PHARMACEUTICALS INTERNATIONAL, INC.; VALEANT PHARMACEUTICALS NORTH AMERICA LLC; WIRRA IP PTY LIMITED; VALEANT PHARMA POLAND SP. Z O.O.; VALEANT PHARMACEUTICALS LUXEMBOURG S.A R.L.; VALEANT PHARMACEUTICALS IRELAND LIMITED
To: THE BANK OF NEW YORK MELLON, AS COLLATERAL AGENT
Reel/Frame 045444/0634 →
SECURITY INTEREST Recorded Feb 26, 2018
From: ATON PHARMA, INC.; BAUSCH & LOMB INCORPORATED; BAUSCH & LOMB PHARMA HOLDINGS CORP.; COMMONWEALTH LABORATORIES, LLC; DOW PHARMACEUTICAL SCIENCES, INC.; ECR PHARMACEUTICALS CO., INC.; LABORATOIRE CHAUVIN S.A.S.; MEDICIS PHARMACEUTICAL CORPORATION; ONPHARMA INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, LTD.; SALIX PHARMACEUTICALS, INC.; SANTARUS, INC.; SOLTA MEDICAL, INC.; SYNERGETICS USA, INC.; TECHNOLAS PERFECT VISION GMBH; VALEANT CANADA LP; VALEANT PHARMACEUTICALS INTERNATIONAL; VALEANT PHARMACEUTICALS INTERNATIONAL, INC.; VALEANT PHARMACEUTICALS NORTH AMERICA LLC; WIRRA IP PTY LIMITED; VALEANT PHARMA POLAND SP. Z O.O.; VALEANT PHARMACEUTICALS LUXEMBOURG S.A R.L.; VALEANT PHARMACEUTICALS IRELAND LIMITED
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 045444/0299 →
SECURITY AGREEMENT Recorded Apr 2, 2015
From: GLYCYX PHARMACEUTICALS, LTD.; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 035364/0396 →
RELEASE OF SECURITY INTEREST Recorded Apr 1, 2015
From: JEFFERIES FINANCE LLC
To: SALIX PHARMACEUTICALS, INC.
Reel/Frame 035356/0519 →
SECURITY AGREEMENT Recorded Jan 2, 2014
From: SALIX PHARMACEUTICALS, INC.
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 031901/0283 →
RELEASE OF SECURITY INTEREST Recorded Jun 1, 2010
From: BANK OF AMERICA, N.A.
To: SALIX PHARMACEUTICALS, INC.
Reel/Frame 024463/0463 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2006
From: INKINE PHARMACEUTICAL COMPANY, INC.
To: SALIX PHARMACEUTICALS, INC.
Reel/Frame 017858/0472 →