BRPI0311700B1 - Processo para a produção de uma preparação em forma de película e preparação em forma de película - Google Patents
Processo para a produção de uma preparação em forma de película e preparação em forma de película Download PDFInfo
- Publication number
- BRPI0311700B1 BRPI0311700B1 BRPI0311700-6A BR0311700A BRPI0311700B1 BR PI0311700 B1 BRPI0311700 B1 BR PI0311700B1 BR 0311700 A BR0311700 A BR 0311700A BR PI0311700 B1 BRPI0311700 B1 BR PI0311700B1
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- BR
- Brazil
- Prior art keywords
- preparation
- gas
- acid
- components
- film
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 25
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
- A61K9/0007—Effervescent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7007—Drug-containing films, membranes or sheets
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Preparation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
| liberado | a | partir da | preparação se | a | mesma é, | por | exemplo, |
| posicionada | na cavidade | bucal e entra | em | contato com a | saliva. A | ||
| formação | de | bolhas de | gás durante | a | ingestão | oral de uma |
| mucosa. | Isto por | sua | vez | auxilia o suprimento de | líquido | em |
| adição | para ambos | os | lados | do wafer. Em contraste, | no caso | do |
| sistema | aderindo | a | mucosa, como pode ocorrer | com wafers |
| componente | de | formação | de | gás e | componentes em | adição da |
| preparação | em | forma de | película. | 0 primeiro e | o segundo | |
| componentes | são | os sócios | de | reação necessários para | uma reação | |
| de formação | de | gás. Cada | um | dos dois | compostos de revestimento | |
| são espalhados | por sobre | um | suporte | e são secos, | assim sendo |
| por exemplo, | de ingestão oral | da | película | - sob | as | condições |
| presentes na | cavidade bucal | tal | como o | valor | do | pH ou a |
| temperatura do | corpo - a reação | de | formação | de gás | será | ativada. |
| Os processos | adequados e as | substâncias | auxiliares | para as | ||
| partículas micro encapsuladas | : são conhecidos | por | aqueles |
| No. | Componente | Proporção de material seca % em peso |
| 1 | Etanol | |
| 2 | PVP | 33% |
| 3 | Ácido cítrico | 20% |
| 4 | NaHCO3 | 35% |
| 5 | Mentol | 7% |
| 6 | Aspartame | 5% |
| No. | Componente | Proporção de material seca % em peso |
| 1 | Etanol | |
| 2 | HPC | 33% |
| 3 | Ácido cítrico | 20% |
| 4 | NaHCO3 | 30% |
| 5 | Sabor de limão | 12% |
| 6 | Aspartame | 5% |
Claims (18)
- REIVINDICAÇÕES1. Processo para a produção de uma preparação em forma de película para a ministração de substâncias a humanos ou animais, referida preparação sendo degradável em um meio aquoso e contendo pelo menos um polímero solúvel em água e um ou mais componentes os quais produzem um gás quando da ação de umidade, na presença de um meio aquoso ou no caso de mudanças de temperatura, pelo revestimento com um ou dois compostos de revestimento sobre um suporte, caracterizado pelo fato que compreende as etapas de:preparar um primeiro composto de revestimento o qual contém um primeiro componente de formação de gás bem como outros componentes da preparação em forma de película pelo dissolver ou suspender referidos componentes em um solvente aquoso ou um agente de suspensão;preparar um segundo composto de revestimento o qual contém um segundo componente de formação de gás bem como outros componentes da preparação em forma de película pelo dissolver ou suspender referidos componentes em um solvente aquoso ou um agente de suspensão, referidos primeiro e segundo componentes de formação de gás sendo parceiros de reação de uma reação de formação de gás;espalhar o primeiro composto de revestimento sobre um suporte e secar o mesmo, formando assim uma primeira película;espalhar o segundo composto de revestimento sobre um suporte e secar o mesmo, formando assim uma segunda película;laminar as duas películas uma sobre a outra; ou as etapas de:preparar um primeiro composto de revestimento o qual contém os componentes da preparação incluindo o componente de formação de gás pelo dissolver ou suspender referidos componentes em um solvente aquoso ou emPetição 870170082454, de 26/10/2017, pág. 13/28
- 2/6 um agente de suspensão, com pelo menos um dos componentes de formação de gás estando presente em uma forma micro encapsulada; e espalhar referido composto de revestimento sobre um suporte e secar o mesmo.2. Processo de acordo com a reivindicação 1, caracterizado pelo fato que o(s) componente(s) de formação de gás e(são) selecionado(s) a partir do grupo compreendendo carbonatos, especialmente carbonato de sódio, carbonato de amônia, carbonato de magnésio, carbonato de potássio e carbonato de hidrogênio, especialmente carbonato de hidrogênio de sódio, e ácidos, especialmente ácidos carboxílicos tais como ácido cítrico, ácido málico, ácido acético, ácido lático, ácido fumárico, ácido glicônico, ácido tartárico, bem como ácidos reguladores, especialmente sais de ácido acético, fosfato de sódio de dihidrogênio ou fosfato de disódio de hidrogênio, tartarato de sódio, ascorbato de sódio.
- 3. Processo de acordo com a reivindicação 2, caracterizado pelo fato que como os componentes de formação de gás uma combinação de pelo menos um componente (a) e pelo menos um componente de formação (b) é usado, referido(s) componente(s) (a) sendo selecionado a partir do grupo de ácidos carboxílicos, preferivelmente a partir do grupo compreendendo ácido cítrico, ácido málico, ácido acético, ácido lático, ácido fumárico, ácido glicônico e ácido tartárico, e referidos componentes (b) sendo selecionado a partir do grupo compreendendo, carbonato de sódio de hidrogênio, carbonato de sódio, carbonato de potássio e carbonato de potássio de hidrogênio.
- 4. Processo de acordo com qualquer uma das reivindicações anteriores, caracterizado pelo fato que a produção é realizada sob a adição dePetição 870170082454, de 26/10/2017, pág. 14/283/6 uma substancia farmacêutica ativa ou de uma combinação de duas ou mais substancias farmacêuticas ativas.
- 5. Processo de acordo com qualquer uma das reivindicações anteriores, caracterizado pelo fato que a produção é realizada sob a adição de um agente de condimentação, preferivelmente mentol.
- 6. Preparação em forma de película degradável em um meio aquoso, para a ministração de substâncias no corpo de um ser humano ou no corpo de um animal, contendo pelo menos um polímero solúvel em água, selecionado dentre álcool polivinílico (PVA), óxido de polietileno, copolímero de metil vinil éter e ácido maléico, derivados de celulose como hidroxipropil metil celulose (HPMC), hidroxipropil celulose (HPC), carboximetil celulose de sódio (NaCMC), metil celulose (MC), hidroxietil celulose (HEC), hidroxipropil etil celulose (HPEC), amido e derivados de amido, gelatinas, polivinil pirrolidona (PVP), goma arábica, pululan, acrilatos e combinações dos mesmos, referida preparação contendo um ou mais componentes os quais produzem um gás quando da ação de umidade ou quando da presença de um meio aquoso ou quando do caso de uma mudança de temperatura, caracterizada pelo fato que pelo menos um dos componentes de formação de gás está presente em uma forma micro encapsulada.
- 7. Preparação em forma de película degradável em um meio aquoso, para a ministração de substâncias no corpo de um ser humano ou no corpo de um animal, contendo pelo menos um polímero solúvel em água, selecionado dentre álcool polivinílico (PVA), óxido de polietileno, copolímero de metil vinil éter e ácido maléico, derivados de celulose como hidroxipropil metil celulose (HPMC), hidroxipropil celulose (HPC), carboximetil celulose de sódio (NaCMC), metil celulose (MC), hidroxietil celulose (HEC), hidroxipropil etil celulose (HPEC), amido e derivados de amido, gelatinas, polivinil pirrolidona (PVP), goma arábica, pululan, acrilatos e combinações dos mesmos, referida preparação contendo umPetição 870170082454, de 26/10/2017, pág. 15/28 ou mais componentes os quais produzem um gás quando da ação de umidade ou quando da presença de um meio aquoso ou quando do caso de uma mudança de temperatura, caracterizada pelo fato que a mesma tem duas camadas de película as quais são conectadas uma com a outra, a primeira camada de película contendo um primeiro componente de formação de gás assim como componentes em adição da preparação em forma de película, e a segunda camada de película contendo um segundo componente de formação de gás assim como componentes em adição da preparação em forma de película, e os referidos primeiro e segundo componentes de formação de gás sendo sócios de reação de uma reação de formação de gás.
- 8. Preparação de acordo com a reivindicação 6 ou 7, caracterizada pelo fato que o(s) componente(s) de formação de gás e(são) selecionados a partir do grupo compreendendo carbonatos, especialmente o carbonato de sódio, o carbonato de amônia, carbonato de magnésio, o carbonato de potássio e o carbonato de hidrogênio, especialmente o carbonato de hidrogênio de sódio, e os ácidos, especialmente os ácidos carboxílicos tais como o ácido cítrico, o ácido málico, o ácido acético, o ácido lático, o ácido fumárico, o ácido glicônico, o ácido tartárico, assim como os ácidos reguladores, especialmente os sais de ácido acético, o fosfato de sódio de di hidrogênio ou o fosfato de di sódio de hidrogênio, o tartarato de sódio, o ascorbato de sódio.
- 9. Preparação de acordo com a reivindicação 8, caracterizada pelo fato que como os componentes de formação de gás uma combinação de pelo menos um componente (a) e pelo menos um componente (b) é usada, o referido componente(s) (a) sendo selecionado a partir do grupo de ácidos carboxílicos, preferivelmente a partir do grupo compreendendo ácido cítrico, ácido málico, ácido acético, ácido lático, ácido fumárico, ácido glicônico e ácido tartárico, e osPetição 870170082454, de 26/10/2017, pág. 16/285/6 referidos componentes, (b) sendo selecionado a partir do grupo compreendendo carbonato de sódio de hidrogênio, carbonato de sódio, carbonato de potássio e carbonato de potássio de hidrogênio.
- 10. Preparação de acordo com qualquer uma das reivindicações 6 a 9, caracterizada pelo fato que referida preparação é capaz de produzir CO2 ou N2, preferivelmente sob a ação da água ou de um meio aquoso ou umidade.
- 11. Preparação de acordo com qualquer uma das reivindicações 6 a 10, caracterizada pelo fato que a mesma produz um ambiente ácido na presença de água.
- 12. Preparação de acordo com qualquer uma das reivindicações 6 a 11, caracterizada pelo fato que referida preparação desintegra-se na presença de água ou de um meio aquoso dentro de 1 segundo a 5 minutos, preferivelmente dentro de 1 segundo a 1 minuto, especialmente preferível dentro de 1 segundo a 30 segundos.
- 13. Preparação de acordo com qualquer uma das reivindicações 6 a 12, caracterizada pelo fato que referida preparação incha na presença de um meio aquoso.
- 14. Preparação de acordo com qualquer uma das reivindicações 6 a 13, caracterizada pelo fato que referida preparação contém uma substância farmacêutica ativa ou uma combinação de duas ou mais substâncias farmacêuticas ativas.
- 15. Preparação de acordo com qualquer uma das reivindicações 6 a 14, caracterizada pelo fato que referida preparação contém um agente de condimentação, preferivelmente, mentol.
- 16. Preparação de acordo com qualquer uma das reivindicações 6 a 15, caracterizada pelo fato que referida preparação compreende pelo menos duasPetição 870170082454, de 26/10/2017, pág. 17/286/6 camadas.
- 17. Preparação de acordo com qualquer uma das reivindicações 6 a 16, caracterizada pelo fato que referida preparação tem uma espessura entre 5 pm e 3 mm, preferivelmente entre 10 pm e 1 mm, especialmente preferivelmente entre 20 pm e 500 mm.
- 18. Preparação de acordo com qualquer uma das reivindicações 6 a 17, caracterizada pelo fato que a mesma é formulada para uma forma de ministração oral, retal ou vaginal para a ministração de agentes farmacêuticos ativos.Petição 870170082454, de 26/10/2017, pág. 18/28
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10224607.6 | 2002-06-04 | ||
| DE10224607A DE10224607B4 (de) | 2002-06-04 | 2002-06-04 | Filmförmige, zerfallsfähige Zubereitungen zur Wirkstofffreisetzung und Verfahren zu deren Herstellung |
| PCT/EP2003/004806 WO2003101420A1 (de) | 2002-06-04 | 2003-05-08 | Filmförmige, zerfallsfähige zubereitungen zur wirkstoff-freisetzung und verfahren zu deren herstellung |
Publications (4)
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| BR0311700A BR0311700A (pt) | 2005-03-08 |
| BRPI0311700B1 true BRPI0311700B1 (pt) | 2018-04-03 |
| BRPI0311700B8 BRPI0311700B8 (pt) | 2019-01-29 |
| BRPI0311700C1 BRPI0311700C1 (pt) | 2021-05-25 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| BRPI0311700A BRPI0311700C1 (pt) | 2002-06-04 | 2003-05-08 | processo para a produção de uma preparação em forma de película e preparação em forma de película |
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| EP (1) | EP1509200B1 (pt) |
| JP (2) | JP4597662B2 (pt) |
| KR (1) | KR101070572B1 (pt) |
| CN (1) | CN100593398C (pt) |
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| BR (1) | BRPI0311700C1 (pt) |
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| DE (2) | DE10224607B4 (pt) |
| ES (1) | ES2314203T3 (pt) |
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| WO (1) | WO2003101420A1 (pt) |
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| RU2257891C1 (ru) * | 2003-12-31 | 2005-08-10 | ООО "Фармстандарт-Фитофарм-НН" | Способ получения композиции в форме шипучих таблеток |
| DE102006027794A1 (de) * | 2006-06-16 | 2007-12-20 | Lts Lohmann Therapie-Systeme Ag | Antihypertonie-Kombinationswafer |
| DE102006027795A1 (de) * | 2006-06-16 | 2007-12-20 | Lts Lohmann Therapie-Systeme Ag | Raucherentwöhnungs-Kombinationswafer |
| DE102006027793A1 (de) * | 2006-06-16 | 2007-12-20 | Lts Lohmann Therapie-Systeme Ag | Opioid-Kombinations-Wafer |
| US7767248B2 (en) | 2007-02-02 | 2010-08-03 | Overly Iii Harry J | Soft chew confectionary with high fiber and sugar content and method for making same |
| US20090011079A1 (en) * | 2007-07-02 | 2009-01-08 | Bestsweet, Inc. | Hard Coated Confectionary Having A Consumable Soft Chewing Core With An Active And Method For Making Same |
| AU2008285409B2 (en) * | 2007-08-07 | 2012-07-05 | Bissell Inc. | Surface treating implement |
| DE102007041588A1 (de) * | 2007-09-01 | 2009-03-05 | Lts Lohmann Therapie-Systeme Ag | Arzneimittel mit Hefe |
| WO2009043588A2 (en) * | 2007-10-02 | 2009-04-09 | LABTEC Gesellschaft für technologische Forschung und Entwicklung mbH | Ph regulating antibacterial films for the oral or vaginal cavity |
| US8282954B2 (en) * | 2008-12-15 | 2012-10-09 | Monosol Rx, Llc | Method for manufacturing edible film |
| WO2010086989A1 (ja) | 2009-01-29 | 2010-08-05 | 日東電工株式会社 | 口腔内フィルム状基剤及び製剤 |
| US20100256197A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Nicotine Dissolving Film With Or Without Menthol |
| US20100256215A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Menthol-Melatonin Dissolving Film |
| JP5751868B2 (ja) | 2010-03-30 | 2015-07-22 | 日東電工株式会社 | フィルム状製剤及びその製造方法 |
| DE102010048408A1 (de) * | 2010-10-15 | 2012-04-19 | Lts Lohmann Therapie-Systeme Ag | Laminat mit verbessertem Wasserretentionsverhalten |
| JP5841433B2 (ja) * | 2012-01-11 | 2016-01-13 | 日東電工株式会社 | 口腔内フィルム状基剤及び製剤 |
| CN103083284B (zh) * | 2013-02-06 | 2014-08-06 | 上海现代药物制剂工程研究中心有限公司 | 膜状制剂及其制备方法 |
| CN103083283B (zh) * | 2013-02-06 | 2014-08-06 | 上海现代药物制剂工程研究中心有限公司 | 氯雷他定膜状制剂 |
| CN103099799B (zh) * | 2013-02-06 | 2014-08-06 | 上海现代药物制剂工程研究中心有限公司 | 复合膜状制剂及其制备方法 |
| CN103127035A (zh) * | 2013-02-21 | 2013-06-05 | 上海现代药物制剂工程研究中心有限公司 | 苯磺酸氨氯地平膜状制剂 |
| CN103142560A (zh) * | 2013-02-21 | 2013-06-12 | 上海现代药物制剂工程研究中心有限公司 | 孟鲁司特钠膜状制剂 |
| CN103142559A (zh) * | 2013-02-21 | 2013-06-12 | 上海现代药物制剂工程研究中心有限公司 | 利培酮膜状制剂 |
| CN103142608B (zh) * | 2013-02-28 | 2015-02-11 | 上海现代药物制剂工程研究中心有限公司 | 磷酸可待因和盐酸异丙嗪复方膜状制剂 |
| CA2937049C (en) | 2013-12-16 | 2024-01-16 | The University Of British Columbia | Self-fueled particles for propulsion through flowing aqueous fluids |
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- 2003-05-08 CN CN03813061A patent/CN100593398C/zh not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| CN100593398C (zh) | 2010-03-10 |
| ATE406870T1 (de) | 2008-09-15 |
| BRPI0311700B8 (pt) | 2019-01-29 |
| US20050175675A1 (en) | 2005-08-11 |
| JP4597662B2 (ja) | 2010-12-15 |
| JP2010209104A (ja) | 2010-09-24 |
| CA2488248A1 (en) | 2003-12-11 |
| RU2004137795A (ru) | 2005-09-10 |
| EP1509200B1 (de) | 2008-09-03 |
| KR101070572B1 (ko) | 2011-10-05 |
| WO2003101420A1 (de) | 2003-12-11 |
| KR20050010025A (ko) | 2005-01-26 |
| BR0311700A (pt) | 2005-03-08 |
| DE10224607B4 (de) | 2008-03-13 |
| RU2316313C2 (ru) | 2008-02-10 |
| AU2003233304B2 (en) | 2008-05-01 |
| EP1509200A1 (de) | 2005-03-02 |
| AU2003233304A1 (en) | 2003-12-19 |
| BRPI0311700C1 (pt) | 2021-05-25 |
| CA2488248C (en) | 2010-09-07 |
| DE50310435D1 (de) | 2008-10-16 |
| ES2314203T3 (es) | 2009-03-16 |
| DE10224607A1 (de) | 2003-12-24 |
| CN1658835A (zh) | 2005-08-24 |
| JP2005537233A (ja) | 2005-12-08 |
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