Quick release pharmaceutical compositions of drug substances
The present invention relates to an oral modified release pharmaceutical composition for the administration of a therapeutically and/or prophylactically effective amount of an active substance (a drug substance) to obtain a relatively fast or quick onset of the therapeutic and/or prophylactic effect. The drug substances contained in a modified release pharmaceutical composition according to the invention are suitably a drug substance which has a very low solubitity under acidic conditions, i.e. under conditions similar to those present in the stomach and/or drug substances which have a pK a value below about 5.5 such as in a range of from about 4 to about 5. The composition is based on a powder comprising a therapeutically and/or prophylactically active substance and has such a particle size that: when the powder is subjected to a sieve analysis, then at least about 90% w/w of the particles passes through sieves 180 μm and the powder is contacted with an aqueous medium to form a particulate composition, which has such a particle size that when the particulate composition is subjected to a sieve analysis, then at least about 50% w/w of the particles passes through sieve 180 μm. Furthermore, the composition, when tested in accordance with the dissolution method (I) defined herein employing 0.07 N hydrochloric acid as dissolution medium, releases at least about 50% w/w of the active substance within the first 20 min of the test.
1. A quick release pharmaceutical composition for oral administration comprising lornoxicam or a pharmaceutically acceptable salt, complex or prodrug thereof,
the composition being in the form of a particulate composition or being based on a particulate composition, wherein either the particles of the particulate composition used in the manufacture of the composition have a mean particle size of at the most 250 micrometers, or
at least 50% w/w of the particles of the particulate composition used in the manufacture of the composition pass through a 180 micrometer sieve;
wherein the quick release pharmaceutical composition contains the lornoxicam in contact with an alkaline substance in a ratio of one part lornoxicam to up to five parts alkaline substance; and
the composition, when tested in accordance with the dissolution method I defined herein employing 0.07 N hydrochloric acid as dissolution medium, releases at least 80% w/w of the lornoxicam within the first 20 minutes of the test.
2. A composition according to claim 1 , further comprising at least one pharmaceutically acceptable excipient.
3. A composition according to claim 2 , wherein the at least one pharmaceutically acceptable excipient is selected from the group consisting of binders, disintegrants, fillers and diluents.
4. A composition according to claim 3 , wherein the composition comprises a filler having binding properties.
5. A composition according to claim 4 , wherein the filler having binding properties is selected from the group consisting of lactose, sugar derivatives, calcium carbonate (CaCO 3 ), tricalcium phosphate (Ca 3 (PO 4 ) 2 ), calcium hydrogen phosphate (CaHPO 4 ) and/or mixtures thereof.
6. A composition according to claim 4 , wherein the filler having binding properties is calcium hydrogen phosphate.
7. A composition according to claim 4 , wherein the filler having binding properties as raw material has a mean particle size of at the most 140 μm.
8. A composition according to claim 1 , comprising a further active drug substance.
9. A composition according to claim 1 , wherein the further active drug substance is an antidepressant, an opioid, a prostaglandine analogue, a glucocorticosteroid, a cytostaticum, a H 2 receptor antagonist, a proton pump inhibitor and/or an antacidum.
10. A composition according to claim 8 , wherein the further active drug substance is misoprostol, methotrexate, cimetidine, ranitidine, pantoprazole, omeprazole, lansoprazole, paracetamol, penicillamine, sulfasalazine and/or auranorfin.
11. A composition according to claim 1 , in unit dosage form, wherein the unit dosage of the composition comprises from 1 to 32 mg of lornoxicam.
12. A composition according to claim 1 , in unit dosage form, wherein the unit dosage comprises from 1 mg to 1.6 g of lornoxicam.
13. A composition according to claim 1 , wherein the unit dosage of the composition contains 1, 2, 3, 4, 8, 12, 16, 20, 24, 28, 32 or 36 mg of lornoxicam.
14. A composition according to claim 1 , wherein the water content in the composition is at the most 5% w/w determined by the LOD (loss on drying) method described herein.
15. A composition according to claim 1 , comprising sodium hydrogen carbonate.
16. A composition according to claim 1 , comprising calcium hydrogen phosphate.
17. A composition according to claim 1 , wherein the alkaline substance is an antacid or an antacid-like substance.
18. A composition according to claim 1 , wherein the quick release pharmaceutical composition is a coated tablet.
19. The composition of claim 1 , comprising lornoxicam, sodium hydrogen carbonate, microcrystalline cellulose, calcium hydrogen phosphate anhydrous, L-HPC, hydroxy propyl cellulose, water, ethanol, and calcium stearate.
20. The composition of claim 1 , comprising lornoxicam, sodium hydrogen carbonate, microcrystalline cellulose, calcium hydrogen phosphate anhydrous, L-HPC, hydroxy propyl cellulose, and calcium stearate.
21. The composition of claim 1 , wherein the composition has a mechanical strength to enable the composition to be coated using traditional coating equipment.
22. The composition of claim 1 , further comprising a filler having binding properties, wherein the composition comprising the binder in the form of tablets having a diameter of 9.5 mm when subjected to a crushing strength test in accordance with Ph. Eur. has a crushing strength of at least about 50N.
23. The composition of claim 1 , wherein the particles of the particulate composition comprises a granulate.
24. A composition according to claim 17 , wherein the alkaline substance is an antacid or an antacid-like substance selected from the group consisting of sodium hydrogen carbonate, magnesium carbonate, magnesium hydroxide and magnesium metasilicate aluminate or mixtures thereof.
25. A composition according to claim 24 , wherein the mean particle size of the antacid-like substance as raw material is at the most 250 μm.