Compositions and methods for reducing methane emissions in ruminant populations
US-2024009291-A1 · Jan 11, 2024 · US
US9339470B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9339470-B2 |
| Application number | US-81030108-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 24, 2008 |
| Priority date | Dec 24, 2007 |
| Publication date | May 17, 2016 |
| Grant date | May 17, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A pharmaceutical composition comprising a solid unit dosage form comprising: (i) ritonavir or a pharmaceutically acceptable salt and ester thereof; (ii) darunavir or a pharmaceutically acceptable salt and ester thereof.
Opening claim text (preview).
The invention claimed is: 1. A pharmaceutical compositon comprising a tablet dosage form comprising: a first layer comprising ritonavir in an amount of 50 mg, collidal silicon dioxide, vinylpyrrolidone-vinyl acetate copolymer, polyoxl 40 hydrogenated castor oil, and dibasic calcium phosphate, and wherein the first layer is absent of darunavir ethanolate; and a second layer comprising the darunavir ethanolate in an amount of 325 mg, microcrystalline cellulose, crospovidone, povidone, collidal silicon dioxide, and magnesium stearate, and wherein the second layer is absent of the ritonavir. 2. The pharmaceutical composition according to claim 1 , wherein the ritonavir of the first layer is present in granules obtained via hot melt extrusion with the collidal silicon dioxide, the vinylpyrrolidone-vinyl acetate copolymer, and the poloxyl 40 hydrogenated castor oil. 3. The pharmaceutical composition according to claim 2 , wherein a melting temperature for the hot melt extrusion ranges from 70° to 200° C. 4. The pharmaceutical composition according to claim 1 , wherein a ratio of the weight of the ritonavir to the weight of the vinylpyrrolidone-vinyl acetate copolymer is from 1:1 to 1:6. 5. The pharmaceutical composition according to claim 1 , wherein the darunavir ethanolate of the second layer is present in granules obtained via wet granulation with povidone. 6. A method of treating HIV or AIDS comprising administering a therapeutically effective amount of the pharmaceutical composition as defined in claim 1 . 7. The pharmaceutical composition according to claim 1 , wherein the tablet dosage form has a film coating. 8. A pharmaceutical composition comprising a tablet dosage form comprising: a first layer comprising ritonavir in an amount of 100 mg, colloidal silicon dioxide, yinylpyrrolidone-vinyl acetate copolymer, sorbitan monolaurate, crospovidone, microcrystalline cellulose, and sodium stearyl monostearate, and wherein the first layer is absent of darunavir; and a second layer comprising the danmavir in an amount of 300 mg, crospovidone, povidone, yellow iron oxide, microcrystalline cellulose, colloidal silicon dioxide, and magnesium stearate, and wherein the second layer is absent of the ritonavir. 9. The pharmaceutical composition according to claim 8 , wherein the ritonavir of the first layer is present in granules obtained via hot melt extrusion with the colloidal silicon dioxide, the yinylpyrrolidone-vinyl acetate copolymer, and sorbitan monolaurate. 10. The pharmaceutical composition according to claim 9 , wherein a melting temperature for the hot melt, extrusion ranges from 70° C. to 200° C. 11. The pharmaceutical composition according to claim 8 , wherein the darunavir of the second layer is present in granules obtained via wet granulation with purified water. 12. The pharmaceutical composition according to claim 8 , wherein a ratio of the weight of the ritonavir to the weight of the vinylpyrrolidone-vinyl acetate copolymer is from 1:1 to 1:6. 13. The pharmaceutical composition according to claim 8 , wherein the tablet dosage form has a film coating. 14. A method of treating HIV or AIDS comprising administering a therapeutically effective amount of the pharmaceutical composition as defined in claim 8 .
for HIV · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Tabletting processes · CPC title
containing drug in at least two layers or in the core and in at least one outer layer · CPC title
Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.