ES2524645A1 - Oral formulation for the treatment of cardiovascular diseases (Machine-translation by Google Translate, not legally binding) - Google Patents
Oral formulation for the treatment of cardiovascular diseases (Machine-translation by Google Translate, not legally binding) Download PDFInfo
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- ES2524645A1 ES2524645A1 ES201330841A ES201330841A ES2524645A1 ES 2524645 A1 ES2524645 A1 ES 2524645A1 ES 201330841 A ES201330841 A ES 201330841A ES 201330841 A ES201330841 A ES 201330841A ES 2524645 A1 ES2524645 A1 ES 2524645A1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/60—Salicylic acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
Abstract
Description
P201330841 05-11-2013 P201330841 11-05-2013
Condiciones de la prueba de disolución: Aparato: USP 1 (cesto) Velocidad de agitación: 100 rpm Dissolution test conditions: Device: USP 1 (basket) Stirring speed: 100 rpm
5 Volumen de disolución: 900 ml Medio de disolución: tampón fosfato a pH 6,8 5 Solution volume: 900 ml Dissolution medium: phosphate buffer at pH 6.8
Los resultados (tabla 11 y figura 5) fueron los siguientes: The results (table 11 and figure 5) were the following:
10 Tabla 11: resultados de disolución de % de AAS disuelto en cápsulas de AAR 10 Table 11: dissolution results of% of ASA dissolved in AAR capsules
- Cápsula de AAR AAR capsule
- Tiempo (min) Time (min)
- % de AAS disuelto % of dissolved AAS
- 0 0
- 0 0
- 15 fifteen
- 73,1 73.1
- 20 twenty
- 86,2 86.2
- 30 30
- 95,3 95.3
- 45 Four. Five
- 97,3 97.3
Como se muestra en la tabla 10 y la tabla 11, la cápsula de AAR que contenía comprimidos de AAS de 50 mg x2 recubiertos con película, que comprendían un recubrimiento de comprimido de 8,7 mg/cm2, muestra valores medios superiores al As shown in Table 10 and Table 11, the AAR capsule containing 50 mg x2 film-coated AAS tablets, comprising a tablet coating of 8.7 mg / cm2, shows average values greater than
15 80 % a los 15 minutos en el caso de pH 4,5 y próximos al 75 % a pH 6,8. 15 80% at 15 minutes in the case of pH 4.5 and close to 75% at pH 6.8.
Una formulación que comprende comprimidos de AAS con un recubrimiento de 8,7 mg/cm2 proporciona más protección y aislamiento al comprimido de ácido acetilsalicílico, haciendo más difícil que el ácido salicílico sublime y desencadene la A formulation comprising ASA tablets with a coating of 8.7 mg / cm2 provides more protection and isolation to the acetylsalicylic acid tablet, making it more difficult for sublime salicylic acid to trigger
20 degradación de los demás componentes, en particular, de la atorvastatina o la rosuvastatina, dentro de la cápsula final. Degradation of the other components, in particular, of atorvastatin or rosuvastatin, within the final capsule.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201330841A ES2524645B1 (en) | 2013-06-06 | 2013-06-06 | Oral formulation for the treatment of cardiovascular diseases |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201330841A ES2524645B1 (en) | 2013-06-06 | 2013-06-06 | Oral formulation for the treatment of cardiovascular diseases |
Publications (2)
Publication Number | Publication Date |
---|---|
ES2524645A1 true ES2524645A1 (en) | 2014-12-10 |
ES2524645B1 ES2524645B1 (en) | 2015-12-02 |
Family
ID=52004086
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES201330841A Active ES2524645B1 (en) | 2013-06-06 | 2013-06-06 | Oral formulation for the treatment of cardiovascular diseases |
Country Status (1)
Country | Link |
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ES (1) | ES2524645B1 (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2307463T1 (en) * | 2001-08-28 | 2008-12-01 | Longwood Pharmaceutical Research, Inc. | COMBINATION DOSAGE FORM CONTAINING A CHOLESTEROL REDUCING AGENT, A RENIN-ANGIOTENSIN INHIBITOR, AND AN ASPIRINE. |
WO2012002919A1 (en) * | 2010-06-30 | 2012-01-05 | Mahmut Bilgic | Pharmaceutical formulations comprising atorvastatin and aspirin |
WO2012081905A2 (en) * | 2010-12-17 | 2012-06-21 | Hanmi Holdings Co. , Ltd. | Pharmaceutical composite formulation comprising hmg-coa reductase inhibitor and aspirin |
WO2012124973A2 (en) * | 2011-03-15 | 2012-09-20 | Boryung Pharmaceutical Co., Ltd | Combined formulation with improved stability |
-
2013
- 2013-06-06 ES ES201330841A patent/ES2524645B1/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2307463T1 (en) * | 2001-08-28 | 2008-12-01 | Longwood Pharmaceutical Research, Inc. | COMBINATION DOSAGE FORM CONTAINING A CHOLESTEROL REDUCING AGENT, A RENIN-ANGIOTENSIN INHIBITOR, AND AN ASPIRINE. |
WO2012002919A1 (en) * | 2010-06-30 | 2012-01-05 | Mahmut Bilgic | Pharmaceutical formulations comprising atorvastatin and aspirin |
WO2012081905A2 (en) * | 2010-12-17 | 2012-06-21 | Hanmi Holdings Co. , Ltd. | Pharmaceutical composite formulation comprising hmg-coa reductase inhibitor and aspirin |
WO2012124973A2 (en) * | 2011-03-15 | 2012-09-20 | Boryung Pharmaceutical Co., Ltd | Combined formulation with improved stability |
Also Published As
Publication number | Publication date |
---|---|
ES2524645B1 (en) | 2015-12-02 |
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