Dispersible dosage form

Patent metadata

Field	Value
Publication number	US-10617648-B2
Application number	US-201615554235-A
Country	US
Kind code	B2
Filing date	Mar 15, 2016
Priority date	Mar 20, 2015
Publication date	Apr 14, 2020
Grant date	Apr 14, 2020

Abstract

The present invention provides for method of improving flowability and loose bulk density of functionalized natural- and/or synthetic calcium carbonate comprising material, to the use of such improved material in ready to use granules and thereof produced dispersible dosage forms.

First claim

The invention claimed is:

1. A method for producing a dispersible dosage form, comprising the steps of:
a) providing a functionalized calcium carbonate-comprising material, which is a reaction product of natural ground or precipitated calcium carbonate with carbon dioxide and one or more acids in an aqueous medium, wherein the carbon dioxide is formed in situ by the acid treatment and/or is supplied from an external source;
b) providing at least one disintegrant;
c) optionally providing at least one further formulating aid;
d) mixing the functionalised calcium carbonate-comprising material of step a), the at least one disintegrant of step b) and the optionally at least one further formulating aid of step c);
e) compacting the mixture obtained in step d) by means of a roller compactor at a compaction pressure in the range from 200 to 2000 kPa (2 to 20 bar) into a ribbon;
f) milling the ribbon of step e) into granules; and
g) sieving the granules of step f) by at least one mesh size;
wherein the functionalised calcium carbonate-comprising material provided in step a) has an intra-particle intruded specific pore volume within the range of 0.15 to 1.35 cm 3 /g, calculated according to the mercury intrusion porosimetry measurement.

2. The method of claim 1 , further comprising a step b1) of providing at least one active ingredient or inactive precursor or both between step b), and step c) or step d).

3. The method of claim 1 , further comprising a step d1) of providing at least one lubricant after step d) and mixing the mixture of step d) with the at least one lubricant of step d1) in a mixing step d2) prior to the compacting step e).

4. The method of claim 2 , further comprising a step d1) of providing at least one lubricant after step d) and mixing the mixture of step d) with the at least one lubricant of step d1) in a mixing step d2) prior to the compacting step e).

5. The method of claim 1 , further comprising a step h) of providing at least one active ingredient and/or inactive precursor and optionally a step i) of providing further additives, and mixing the granules of step f) with the at least one active ingredient and/or inactive precursor of step g) and the optionally provided further additives of step h).

6. The method of claim 1 , further comprising a final step j) of tableting the material obtained in the last step.

7. The method according to claim 1 , wherein the natural ground calcium carbonate is selected from calcium carbonate comprising minerals selected from the group consisting of marble, chalk, limestone, dolomite and any mixture thereof; and the precipitated calcium carbonate is selected from the group of precipitated calcium carbonate having aragonitic, vateritic, or calcitic mineralogical crystal forms, and any mixture thereof.

8. The method of claim 1 , wherein the functionalized calcium carbonate-comprising material is a reaction product of natural ground calcium carbonate with carbon dioxide and phosphoric acid in an aqueous medium, wherein the carbon dioxide is formed in situ by the acid treatment and/or is supplied from an external source.

9. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material has a BET specific surface area of from 20 m 2 /g to 450 m 2 /g, measured using the nitrogen and BET method according to ISO 9277.

10. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material has a BET specific surface area of from 20 m 2 /g to 140 m 2 /g, measured using the nitrogen and BET method according to ISO 9277.

11. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material comprises particles having a volume median grain diameter d 50 of from 2 μm to 50 μm.

12. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material comprises particles having a volume median grain diameter d 50 of from 1 μm to 35 μm.

13. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material has an intra-particle intruded specific pore volume within the range of 0.30 to 1.30 cm 3 /g, calculated according to the mercury intrusion porosimetry measurement.

14. The method according to claim 1 , wherein the functionalised calcium carbonate-comprising material has an intra-particle intruded specific pore volume within the range of 0.40 to 1.25 cm 3 /g, calculated according to the mercury intrusion porosimetry, measurement.

15. The method according to claim 1 , wherein the granules have a flowability from 1.36 g/s to 5.75 g/s when compacted at 1000 kPa (10 bar) and sieved with mesh sizes of 180 μm, 250 μm, 355 μm, 500 μm, and 710 μm, and the granules with size less than 180 μm and more than 710 μm were excluded, when measured according to European Pharmacopeia, 7 th Ed Strassbourg (France): Council of Europe 2011, at an opening diameter from 5 min to 9 mm.

16. The method according to claim 1 , wherein the granules have a loose bulk density of 0.65 g/cm 3 when compacted at 1000 kPa (10 bar) and sieved with mesh sizes of 180 μm, 250 μm, 355 μm, 500 μm, and 710 μm, and the granules with size less than 180 μm and more than 710 μm were excluded.

17. The method according to claim 1 , wherein the at least one disintegrant is selected form the group consisting of modified cellulose gums, insoluble cross-linked polyvinylpyrrolidones, starch glycolates, micro crystalline cellulose, pregelatinized starch, sodium carboxymethyl starch, low-substituted hydroxypropyl cellulose, homopolymers of N-vinyl-2-pyrrolidone, alkyl-, hydroxyalkyl-, carboxyalkyl-cellulose esters, alginates, microcrystalline cellulose and its polymorphic forms, ion exchange resins, gums, chitin, chitosan, clays, gellan gum, crosslinked polacrillin copolymers, agar, gelatine, dextrines, acrylic acid polymers, carboxymethylcellulose sodium/calcium, hydroxypropyl methyl cellulose phthalate, shellac, and any mixture thereof.

18. The method according to claim 1 , wherein the at least one disintegrant is a modified cellulose gum.

19. The method according to claim 1 , wherein the at least formulating aid is at least one inner-phase lubricant and/or outer-phase lubricant; and is provided in a total amount from 0.1 wt.-% to 10.0 wt.-%, based on the total weight of the functionalized calcium carbonate-comprising material of step a).

20. The method according to claim 1 , wherein the at least formulating aid is at least one inner-phase lubricant and/or outer-phase lubricant; and is provided in a total amount from 0.3 wt.-% to 5.0 wt.-%, based on the total weight of the functionalized calcium carbonate-comprising material of step a).

Assignees

• Omya Int Ag

Inventors

• Wagner-Hattler Leonie
• Puchkov Maxim
• Huwyler Jörg
• Stirnimann Tanja
• Diaz Quijano Carolina
• Schoelkopf Joachim
• Gane Patrick A C
• Gerard Daniel E

Classifications

• A61K9/2009

  Inorganic compounds · CPC title

• A61K8/19

  containing inorganic ingredients · CPC title

• A61K9/2095

  Tabletting processes · CPC title

• A61K9/2068

  Compounds of unknown constitution, e.g. material from plants or animals (oils, fats, waxes, shellac A61K9/2013) · CPC title

• A61K9/1664

  Compounds of unknown constitution, e.g. material from plants or animals (oils, fats, waxes, shellac A61K9/1617) · CPC title