Compositions for treating chronic inflammation and inflammatory diseases

US9326958B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9326958-B2
Application numberUS-201414520141-A
CountryUS
Kind codeB2
Filing dateOct 21, 2014
Priority dateOct 29, 2010
Publication dateMay 3, 2016
Grant dateMay 3, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The present specification discloses pharmaceutical compositions, methods of preparing such pharmaceutical compositions, and methods and uses of treating a chronic inflammation and/or an inflammatory disease in an individual using such pharmaceutical compositions.

First claim

Opening claim text (preview).

The invention claimed is: 1. A pharmaceutical composition comprising: a) a therapeutically-effective amount of a pharmaceutically-acceptable form of a non-steroidal anti-inflammatory drug (NSAID); b) about 1% (v/v) to about 20% (v/v) of a pharmaceutically-acceptable polyethylene glycol (PEG) polymer; and c) at least 50% (v/v) of a pharmaceutically-acceptable lipid-adjuvant, wherein the pharmaceutically-acceptable lipid-adjuvant is a fatty acid having at least 12 carbons, a glycerolipid, a sphingolipid, a sterol lipid, a prenol lipid, a saccharolipid, or a polyketide, wherein the pharmaceutical composition is formulated to have a melting point temperature of about 25° C. or higher. 2. The pharmaceutical composition according to claim 1 , wherein the NSAID comprises a non-selective cyclo-oxygenase inhibitor, a selective cyclooxygenase 1 inhibitor, a selective cyclooxygenase 2 inhibitor or any combination thereof. 3. The pharmaceutical composition according to claim 1 , wherein the NSAID comprises a pharmaceutically-acceptable form of a salicylate derivative NSAID, a pharmaceutically-acceptable form of a p-amino phenol derivative NSAID, a pharmaceutically-acceptable form of a propionic acid derivative NSAID, a pharmaceutically-acceptable form of an acetic acid derivative NSAID, a pharmaceutically-acceptable form of an enolic acid derivative NSAID, a pharmaceutically-acceptable form of a fenamic acid derivative NSAID, or any combination thereof. 4. The pharmaceutical composition according to claim 3 , wherein the propionic acid derivative NSAID comprises a pharmaceutically-acceptable form of an Alminoprofen, a pharmaceutically-acceptable form of a Benoxaprofen, a pharmaceutically-acceptable form of a Dexketoprofen, a pharmaceutically-acceptable form of a Fenoprofen, a pharmaceutically-acceptable form of a Flurbiprofen, a pharmaceutically-acceptable form of an Ibuprofen, a pharmaceutically-acceptable form of an Indoprofen, a pharmaceutically-acceptable form of a Ketoprofen, a pharmaceutically-acceptable form of a Loxoprofen, a pharmaceutically-acceptable form of a Naproxen, a pharmaceutically-acceptable form of an Oxaprozin, a pharmaceutically-acceptable form of a Pranoprofen, or a pharmaceutically-acceptable form of a Suprofen. 5. The pharmaceutical composition according to claim 4 , wherein the propionic acid derivative NSAID is a pharmaceutically-acceptable form of an Ibuprofen. 6. The pharmaceutical composition according to claim 1 , wherein the NSAID comprises an ester of the NSAID. 7. The pharmaceutical composition according to claim 1 , wherein the concentration of the NSAID is at least 50 mg/mL. 8. The pharmaceutical composition according to claim 1 , wherein the PEG polymer is in an amount of less than about 15% (v/v). 9. The pharmaceutical composition according to claim 1 , wherein the PEG polymer is in an amount of about 8% (v/v) to about 15% (v/v). 10. The pharmaceutical composition according to claim 9 , wherein the PEG polymer is in an amount of about 8% (v/v) to about 12% (v/v). 11. The pharmaceutical composition according to claim 1 , wherein the PEG polymer is in an amount of about 4% (v/v) to about 10% (v/v). 12. The pharmaceutical composition according to claim 11 , wherein the PEG polymer is in an amount of about 6% (v/v) to about 10% (v/v). 13. The pharmaceutical composition according to claim 1 , wherein the PEG polymer is a low molecular mass liquid or low-melting solid. 14. The pharmaceutical composition according to claim 13 , wherein the PEG polymer is less than about 2,000 g/mol. 15. The pharmaceutical composition according to claim 14 , wherein the PEG polymer comprises PEG 100, PEG 200, PEG 300, PEG 400, PEG 500, PEG 600, PEG 700, PEG 800, PEG 900, PEG 1000, or any combination thereof. 16. The pharmaceutical composition according to claim 1 , wherein the lipid-adjuvant is in an amount of at least 60% (v/v). 17. The pharmaceutical composition according to claim 1 , wherein the lipid-adjuvant is in an amount of about 50% (v/v) to about 95% (v/v). 18. The pharmaceutical composition according to claim 1 , wherein the lipid-adjuvant comprises a saturated fatty acid, an unsaturated fatty acid, or any combination thereof. 19. The pharmaceutical composition according to claim 1 , wherein the lipid-adjuvant comprises a monoglyceride, an acetylated monoglyceride, a diglyceride, an acetylated diglyceride, a triglyceride, an acetylated triglyceride, or any combination thereof. 20. The pharmaceutical composition according to claim 19 , wherein the amount of the monoglyceride is at least 15% (v/v). 21. The pharmaceutical composition according to claim 20 , wherein the amount of the monoglyceride is at least 20% (v/v). 22. The pharmaceutical composition according to claim 19 , wherein the amount of the triglyceride is at least 30% (v/v). 23. The pharmaceutical composition according to claim 22 , wherein the amount of the triglyceride is at least 35% (v/v).

Assignees

Inventors

Classifications

  • Antianaemics · CPC title

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure · CPC title

  • Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors · CPC title

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What does patent US9326958B2 cover?
The present specification discloses pharmaceutical compositions, methods of preparing such pharmaceutical compositions, and methods and uses of treating a chronic inflammation and/or an inflammatory disease in an individual using such pharmaceutical compositions.
Who is the assignee on this patent?
Infirst Healthcare Ltd
What technology area does this patent fall under?
Primary CPC classification A61K31/192. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue May 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).