IP Library Granted Patent US 10,280,177
Granted Patent B2
US 10,280,177 · App. 15/153,636 · Granted May 7, 2019

Use of polyols to obtain stable polymorphous forms of rifaximin

Inventors: Paola Maffei (Bologna, IT); Milena Bachetti (Bologna, IT); Giuseppe Bottoni (Bologna, IT); Giuseppe Claudio Viscomi (Bologna, IT)
Assignee: ALFASIGMA S.P.A.
C07D491/22A61K9/1617A61K9/1623A61K9/1652A61K9/2013A61K9/2054A61K9/2081A61K9/28A61K9/501A61K9/5015A61K9/5026A61K31/437A61K47/10A61K47/26C07B2200/13
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Quick Facts
Patent No.
US 10,280,177
App. No.
15/153,636
Granted
May 7, 2019
Kind
B2
Abstract

Polyols stabilize polymorphous form of rifaximin, in particular the β form. When polyols having at least two hydroxy groups are added to rifaximin powder, polymorph β is stable and remains stable in time independently from the environment humidity. In this invention a method to prepare formulations constituted by pure and stable polymorphous forms able to give a pharmaceutical product is described.

Claims (12)

1. A pharmaceutical composition comprising a stabilized polymorphous form β of rifaximin comprising one or more polyol stabilizers within granules or gastroresistant granules and an excipient, the one or more polyol stabilizers selected from the group consisting of 1,2-propanediol, 1,2,3-propanetriol and a compound having general formula H—[O—CH 2 —CH 2 ] n —OH, wherein n is between 2 and 16,

wherein the stabilized polymorphous form β of rifaximin has a residual water content lower than 4.5%.

2. The pharmaceutical composition of claim 1 , wherein the one or more polyol stabilizers is 1,2,3-propanetriol.

3. The pharmaceutical composition of claim 1 , wherein the one or more polyol stabilizers is 1,2-propanediol.

4. The pharmaceutical composition of claim 1 , wherein the one or more polyol stabilizers further comprise polyols having two to seven carbon atoms and two to seven hydroxyl groups.

5. The pharmaceutical composition of claim 1 , wherein the stabilized polymorphous form β of rifaximin has an X-ray diffraction spectra characterized by peaks at the values of the diffraction angles at about:

5.3°±0.2, 6.7°±0.2, 7.7°±0.2, 8.9°±0.2, 10.4°±0.2, and 12.3°±0.2, 17.7°±0.2, 18.2°±0.2; 18.6°±0.2 and 20.7°±0.2 2θ.

6. The pharmaceutical composition according to claim 1 , wherein the granules or gastroresistant granules further comprise diluents in an amount from 1% (w/w) to 20% (w/w).

7. The pharmaceutical composition of claim 1 , wherein the excipient is selected from the group consisting of diluents, ligands, lubricants, disintegrants, dyes, flavors and sweeteners.

8. The pharmaceutical composition of claim 1 , wherein the composition is in form of a tablet.

9. The pharmaceutical composition of claim 8 , wherein the tablet is coated with coating excipients.

10. The pharmaceutical composition of claim 1 , wherein the composition is in thermos-welded bags.

Assignments (3)
CHANGE OF ADDRESS Recorded Oct 15, 2019
From: ALFASIGMA S.P.A.
To: ALFASIGMA S.P.A.
Reel/Frame 050727/0652 →
MERGER Recorded Nov 14, 2017
From: ALFA WASSERMANN S.P.A.
To: ALFASIGMA S.P.A.
Reel/Frame 045061/0645 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2016
From: MAFFEI, PAOLA; BACHETTI, MILENA; BOTTONI, GIUSEPPE; VISCOMI, GIUSEPPE CLAUDIO
To: ALFA WASSERMANN S.P.A.
Reel/Frame 039138/0848 →
Priority Claims (1)
IT MI2006A1692 · Sep 5, 2006 · national
Continuity (4)
Continuation 14263845 · Apr 28, 2014
Continuation 13544945 · Jul 9, 2012
Division 12439094
Related Publication 20170101417A1 · Apr 13, 2017