WO2000047190A2 - Method for producing film-type dosage forms - Google Patents
Method for producing film-type dosage forms Download PDFInfo
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- WO2000047190A2 WO2000047190A2 PCT/EP2000/000739 EP0000739W WO0047190A2 WO 2000047190 A2 WO2000047190 A2 WO 2000047190A2 EP 0000739 W EP0000739 W EP 0000739W WO 0047190 A2 WO0047190 A2 WO 0047190A2
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- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/70—Fixation, conservation, or encapsulation of flavouring agents
- A23L27/79—Fixation, conservation, or encapsulation of flavouring agents in the form of films
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P20/00—Coating of foodstuffs; Coatings therefor; Making laminated, multi-layered, stuffed or hollow foodstuffs
- A23P20/20—Making of laminated, multi-layered, stuffed or hollow foodstuffs, e.g. by wrapping in preformed edible dough sheets or in edible food containers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
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- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Definitions
- the present invention relates to film-like dosage forms for use as cosmetic, pharmaceutical or food products.
- EP 0 216 762 presents a water-soluble film made of starch, gelatin, glycerin or sorbitol, which is coated by means of a roller application process. It is mentioned briefly that such dosage forms can also be produced for chemical reagents, flavorings and the like.
- a formulation that is fundamentally suitable for the production of film-shaped systems is presented in EP 0 460 588.
- particular advantages are seen in the composition of 20 to 60 percent by weight film former, 2 to 40% gel former, 0.1 to 35 percent by weight of active ingredient (here: flavoring) and a maximum of 40 percent by weight of an inert filler.
- DE 36 30 603 sees particular advantages in designing the flat dosage form on a carrier material (separating film) in a dose-wise manner.
- the object of this invention is to provide processes for the production of sheet-like active substance carriers which enable an exact and reproducible coating quality, prevent the finally produced film pieces from adhering to one another in the stack and avoid contamination and too high heat loads are available at high process speeds.
- the object is achieved according to the present invention in that the coating of the solution of hydrophilic polymers with added active ingredients and other auxiliaries is immediately followed by an overflow of moderately warm (30-50 ° C.) air, then the temperature is slightly increased (35 -80 ° C), followed by a reconditioning phase at 25-50 ° C.
- the process speed is advantageously regulated in such a way that a relative substrate moisture (equivalent moisture or equivalent air humidity) of 50-75% RH, preferably 60-68% RH, is not left in any case.
- the method according to the invention can be applied to any form of sheet-like products, for example for use as food, pharmaceuticals or cosmetics, which in a coating process consist of a solvent, in particular re water, liquefied mass, which contains solid, hydrophilic raw materials and optionally further components, can be produced.
- Suitable substances are, for example, carbonates, phosphates, silicates, or sulfates of alkaline earth metals, zinc oxide, titanium dioxide or other color pigments, talc, lactose, cyclodextrins or starch and starch derivatives, provided that they form their own, solid, disperse phase in the end product.
- Aromas which can be used with this invention are essentially essential oils (volatile, water-insoluble distillates from fragrant plant components) and other volatile, fragrant substances which have a limited miscibility with water.
- the mass is obtained, for example, by sprinkling, kneading or slowly digesting the solid components in the solvent (usually water, but also, for example, ethanol, Acetone and other compatible, physiologically acceptable solvents and their mixtures are used). If contained in the recipe, the pre-weighed amount of flavoring and other liquid, lipophilic additives are added to this phase with slow stirring. In the interest of the objective of the invention, it has proven to be very advantageous with regard to a more uniform nature to homogenize the mass before coating via a high-speed homogenizer.
- the solvent usually water, but also, for example, ethanol, Acetone and other compatible, physiologically acceptable solvents and their mixtures are used.
- the mass is coated onto a substrate by brushing, knife coating or extrusion processes and is dried in a drying channel consisting of at least three independently temperature-controlled zones.
- the substrate can in principle be made from substrates known to those skilled in the art and widely used, e.g. Polyethylene terephthalate, polyethylene, polypropylene, polycarbonate, polyurethane exist. Laminates of these materials with other polymers, paper, glass fibers and other structure formers are also used to increase the tear resistance. Measures such as siliconization, fluorination, acid treatment or corona treatment can be useful to regulate the surface adhesion, but in individual cases they need to be clarified as to their physiological compatibility for the respective application.
- the aim of the invention is regularly achieved when the drying with initially increasing, at the latest in in the last zone then process temperature reduced by 10 ° C again.
- the process speed is advantageously set so that a product with an equivalent air humidity of 50-75% RH, preferably 60-68% RH, is obtained.
- the products obtained proved to be surface-stable, flexible and unbreakable and largely tear-resistant.
- the resulting surfaces have practically no "cold flow", so they are basically dimensionally stable.
- the film can be removed from the base without noticeable stretching and processed separately.
- the film-shaped products produced preferably have a thickness between 20 and 300 ⁇ m; their size can advantageously be 0.5 to 12 cm 2 .
- the subsequent packaging can be done individually or in a stack, for example in sealed bags or dispensers.
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- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Polymers & Plastics (AREA)
- Pharmacology & Pharmacy (AREA)
- Manufacturing & Machinery (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Biomedical Technology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Physiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Preparation (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- General Preparation And Processing Of Foods (AREA)
- Laminated Bodies (AREA)
- Cosmetics (AREA)
- Wrappers (AREA)
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Abstract
Description
Verfahren zur Herstellung folienförπ-iger DarreichungsformenProcess for the production of film-like dosage forms
Die vorliegende Erfindung betrifft folienförmige Darreichungsformen zur Anwendung als kosmetische, pharmazeutische oder lebens itteltechnische Produkte.The present invention relates to film-like dosage forms for use as cosmetic, pharmaceutical or food products.
Im Mundbereich und auf den Schleimhäuten des Mundes anzuwendende flächige Darreichungsformen sind bekannt. So beschreibt bereits US 3 444 858 (Russell, 1969) Medikamentstreifen auf Basis eines gelatineartigen Materials.Flat dosage forms to be used in the mouth area and on the mucous membranes of the mouth are known. No. 3,444,858 (Russell, 1969) already describes medicament strips based on a gelatin-like material.
In EP 0 216 762 wird eine wasserlösliche Folie aus Stärke, Gelatine, Glycerin oder Sorbit vorgestellt, die mittels eines Walzenauftragsverfahrens beschichtet wird. Es wird dabei kurz erwähnt, daß sich solche Dosierungsformen auch für chemische Reagenzien, Aromastoffe und dergleichen herstellen lassen.EP 0 216 762 presents a water-soluble film made of starch, gelatin, glycerin or sorbitol, which is coated by means of a roller application process. It is mentioned briefly that such dosage forms can also be produced for chemical reagents, flavorings and the like.
Eine zur Herstellung folienförmiger Systeme grundsätzlich geeignete Formulierung wird in EP 0 460 588 vorgestellt. Hier werden besondere Vorteile in der Zusammensetzung aus 20 bis 60 Gewichtsprozent Filmbildner, 2 bis 40 % Gelbild- ner, 0,1 bis 35 Gewichtsprozent Wirkstoff (hier: Aromastoff) und maximal 40 Gewichtsprozent eines inerten Füllstoffes gesehen.A formulation that is fundamentally suitable for the production of film-shaped systems is presented in EP 0 460 588. Here, particular advantages are seen in the composition of 20 to 60 percent by weight film former, 2 to 40% gel former, 0.1 to 35 percent by weight of active ingredient (here: flavoring) and a maximum of 40 percent by weight of an inert filler.
DE 36 30 603 sieht besondere Vorteile darin, die flächige Dosierungsform auf einem Trägermaterial (Trennfilm) dosisweise abziehbar zu gestalten.DE 36 30 603 sees particular advantages in designing the flat dosage form on a carrier material (separating film) in a dose-wise manner.
US 4 128 445 und 4 197 289 (Sturzenegger, 1978) gehen auf mögliche technische Lösungen bei der Beladung mit Wirkstoffen ein. Für arzneimittelhaltige folienför ige Systeme werden auch Vorteile in einem zweischichtigen Aufbau aus einer wasser- quellbaren Schicht und einem wasserunlöslichen Barrierefilm gesehen (US 5 047 244) .US 4 128 445 and 4 197 289 (Sturzenegger, 1978) deal with possible technical solutions when loading with active substances. For drug-containing film-shaped systems, advantages are also seen in a two-layer structure consisting of a water-swellable layer and a water-insoluble barrier film (US Pat. No. 5,047,244).
Einige hydrophile Filmbildner, insbesondere Pullulan und andere Glucane, aber auch Cellulosederivate weisen bei der Herstellung solcher Filme mangelhafte Benetzung auf üblichen Beschichtungsmedien auf. Die Folge kann vorzeitige oder schwierige Substratablösung sowie ungleichmäßige resultierende Foliendicke sein. Zur Abhilfe empfiehlt US 4 562 020 die Verwendung eines im Prozeß als Schlaufe umlaufenden Substrates auf Basis unpolarer hitzestabiler Polymere, welches innerhalb des Prozesses ständig einer oberflächigen Korona-Behandlung unterzogen wird und damit ständig neu eine ausreichend sicher benetzende, polare Oberfläche erhält. Es wird bei Trocknungstemperaturen zwischen 40 und 110 °C gearbeitet; in den Beispielen finden sich Temperaturen zwischen 60 und 85 °C.Some hydrophilic film formers, in particular pullulan and other glucans, but also cellulose derivatives, have inadequate wetting on conventional coating media in the production of such films. The consequence can be premature or difficult substrate detachment and uneven resulting film thickness. To remedy this, US Pat. No. 4,562,020 recommends the use of a substrate rotating in the process as a loop on the basis of non-polar, heat-stable polymers, which is constantly subjected to a surface corona treatment during the process and thus constantly receives a sufficiently securely wetting, polar surface. It works at drying temperatures between 40 and 110 ° C; In the examples there are temperatures between 60 and 85 ° C.
Als nachteilig erweisen sich die auf den beschriebenen reinen Foliensubstraten hergestellten Aroma-Folien wegen ihrer beidseitigen Glätte. Solche Produkte eignen sich nur eingeschränkt zur Weiterverarbeitung und Anwendung in durch Fo- lienschnitt gebildeten Stapeln. Solche Stapel von Folienstücken oder -stanzlingen, wie sie zur Anwendung beim Verbraucher häufig in geeigneten Dosierspendern angeboten werden, neigen zur gegenseitigen Verklebung, die eine sichere Entnahme stark erschwert. Da solche folienförmigen Darreichungsformen wegen ihres geringen Flächengewichtes (typisch ca. 10 bis 80 g/m2 ) zu statischer Aufladung neigen und die Oberflächen gleichzeitig wegen der späteren leichteren Entnahme gegeneinander verschiebbar ausgeführt sind, ist dieser Aspekt nicht nur bei der Verwendung, sondern auch bei der Prozeßtechnologie störend. Eine dritte Anforderung an den Prozeß ist die Vermeidung von hitzebedingten Aromaverlusten bei maximaler Prozeßgeschwindigkeit, für die sich auch aus dem Stand der Technik keine Hinweise ergeben.The aroma films produced on the described pure film substrates prove to be disadvantageous because of their smoothness on both sides. Such products are only of limited suitability for further processing and use in stacks formed by foil cutting. Such stacks of pieces of film or die cuts, as are often offered in suitable dosing dispensers for use by the consumer, tend to stick to one another, which makes safe removal very difficult. Since such film-like dosage forms tend to be statically charged due to their low basis weight (typically approx. 10 to 80 g / m 2 ) and the surfaces are designed to be displaceable relative to one another because of the later easier removal, this aspect is not only in use but also in the process technology disruptive. A third requirement for the process is the avoidance of heat-related loss of aroma at maximum process speed, for which there are no indications from the prior art either.
Aus diesen bisher im Stand der Technik nicht gelösten Anforderungen ergibt sich die Aufgabe dieser Erfindung, Verfahren zur Herstellung flächenförmiger Wirkstoffträger bereitszustellen, welche eine genaue und reproduzierbare Be- schichtungsgüte ermöglichen, die Anhaftung der final hergestellten Folienstücke aneinander im Stapel verhindern und unter Vermeidung von Kontamination und allzu hoher Hitzebelastung mit hoher Prozeßgeschwindigkeit erhältlich sind.From these requirements which have not yet been solved in the prior art, the object of this invention is to provide processes for the production of sheet-like active substance carriers which enable an exact and reproducible coating quality, prevent the finally produced film pieces from adhering to one another in the stack and avoid contamination and too high heat loads are available at high process speeds.
Die Aufgabe wird gemäß der vorliegenden Erfindung dadurch gelöst, daß sich an die Beschichtung der Lösung hydrophiler Polymere mit zugesetzten Wirk- und weiteren Hilfsstoffen unmittelbar eine Überströmung mit mäßig warmer (30-50°C) Luft anschließt, sodann die Temperatur leicht erhöht wird (35-80°C), worauf sich zuletzt eine Rekonditionierungsphase bei 25-50°C anschließt. Die Prozeßgeschwindigkeit wird dabei vorteilhaft so einreguliert, daß in jedem Fall eine relative Substratfeuchte (Äquivalentfeuchte oder äquivalente Luftfeuchte) von 50-75% r.F., bevorzugt 60-68% r.F., nicht verlassen wird.The object is achieved according to the present invention in that the coating of the solution of hydrophilic polymers with added active ingredients and other auxiliaries is immediately followed by an overflow of moderately warm (30-50 ° C.) air, then the temperature is slightly increased (35 -80 ° C), followed by a reconditioning phase at 25-50 ° C. The process speed is advantageously regulated in such a way that a relative substrate moisture (equivalent moisture or equivalent air humidity) of 50-75% RH, preferably 60-68% RH, is not left in any case.
Durch Verwendung oberflächenrauher Substrate, bevorzugt von Thermoplasten aus Polypropylen, Polyethylen, Polyethylen- terephthalat, Polycarbonat und Laminaten dieser Polymere, besonders bevorzugt polyethylenbeschichtetem Papier, wird eine Verklebung der später hergestellten Folieneinzelstücke im Stapel wirksam vermieden.By using substrates with a rough surface, preferably thermoplastics made of polypropylene, polyethylene, polyethylene terephthalate, polycarbonate and laminates of these polymers, particularly preferably polyethylene-coated paper, sticking of the individual film pieces produced later is effectively avoided in the stack.
Das erfindungsgemäße Verfahren ist auf jede Form flächenförmiger Produkte zum Beispiel zum Einsatz als Lebensmittel, Arzneimittel oder Kosmetikum anwendbar, die in einem Beschichtungsprozeß aus einer durch Lösemittel, insbesonde- re Wasser, verflüssigten Masse, die feste, hydrophile Grundstoffe und optional weitere Bestandteile enthält, herstellbar sind.The method according to the invention can be applied to any form of sheet-like products, for example for use as food, pharmaceuticals or cosmetics, which in a coating process consist of a solvent, in particular re water, liquefied mass, which contains solid, hydrophilic raw materials and optionally further components, can be produced.
Diese hydrophilen Grundstoffe können Polymere wie Stärke und ihre Derivate, Agar-Agar, Gelatine, Cellulose und Cel- lulosederivate, Alginsäure, Galactomannan, Carrageen, andere für das jeweilige Einsatzgebiet zulässige pflanzliche Gummen, Pullulan und andere Glucane, Dextran, Polyvinylpyr- rolidon-, Polyvinylalkohol- oder Polyacrylsäure-Ho o- und -copolymere sein. Der verwendete Polyvinylalkohol ist vorteilhafterweise eine teilhydrodysierte Form, bei der zwischen 1 und 20%, besonders bevorzugt ca. 12% der Hydroxylgruppen durch Acetylgruppen ersetzt sind.These hydrophilic raw materials can include polymers such as starch and their derivatives, agar-agar, gelatin, cellulose and cellulose derivatives, alginic acid, galactomannan, carrageenan, other vegetable gums permissible for the respective field of application, pullulan and other glucans, dextran, polyvinylpyrrolidone, Polyvinyl alcohol or polyacrylic acid ho o and copolymers. The polyvinyl alcohol used is advantageously a partially hydrodysed form in which between 1 and 20%, particularly preferably approximately 12%, of the hydroxyl groups are replaced by acetyl groups.
Das erfindungsgemäße Verfahren wirkt sich insbesondere bei problematischen Massen aus, die hohe Anteile an Pullulan, Carrageen oder Cellulosestern enthalten.The method according to the invention has an effect in particular in the case of problematic compositions which contain high proportions of pullulan, carrageenan or cellulose esters.
Hydrophile Zusätze geringen Molekulargewichts können als Strukturbildner ebenfalls eingesetzt werden; sie erfüllen meist anwendungsspezifische Ziele. Hier kommen u.a. Zucker, Zuckeralkohole, Zuckerersatzstoffe, organische Säuren, Po- lyethylenglycol infrage.Hydrophilic additives of low molecular weight can also be used as structure formers; they mostly meet application-specific goals. Here come Sugar, sugar alcohols, sugar substitutes, organic acids, polyethylene glycol in question.
Auch feste Stoffe, die wegen geringer Löslichkeit keine molekulardisperse Mischung oder Lösung im Grundmaterial eingehen, können enthalten sein. Geeignete Substanzen sind zum Beispiel Carbonate, Phosphate, Silicate, oder Sulfate der Erdalkalimetalle, Zinkoxid, Titandioxid oder andere Farbpigmente, Talkum, Lactose, Cyclodextrine oder Stärke und Stärkederivate, sofern sie im Endprodukt eine eigene, feste disperse Phase bilden.It can also contain solid substances that do not form a molecularly disperse mixture or solution in the base material due to their low solubility. Suitable substances are, for example, carbonates, phosphates, silicates, or sulfates of alkaline earth metals, zinc oxide, titanium dioxide or other color pigments, talc, lactose, cyclodextrins or starch and starch derivatives, provided that they form their own, solid, disperse phase in the end product.
Die vorstehende Auflistung ist beispielhaft und kann durch dem Fachmann bekannte funktionsgleiche Stoffe ergänzt werden. Wirkkomponenten können zum Beispiel arzneiliche oder kosmetische Wirkstoffe, diätetische Zusatzstoffe zu Lebensmitteln, Farbstoffe oder Diagnostika sein. Insbesondere ist der erfindungsgemäße Prozeß bei den sonst wegen ihrer Flüchtigkeit schwer verarbeitbaren Aromastoffen anwendbar. Bei mit dieser Erfindung einsetzbaren Aromen handelt es sich im wesentlichen um ätherische Öle (flüchtige, wasserunlösliche Destillate aus duftenden Pflanzenbestandteilen) und andere flüchtige, duftende Substanzen, die eine begrenzte Mischbarkeit mit Wasser aufweisen. Beispielhaft seien hier z.B. Phenylethanol als Bestandteil von Rosen- duftaro en, Menthol, Eucalyptol (Cineol), Camphen und Pinen in pfefferminzartig-frischen Aromen, appetitanregende Aromastoffe (Gewürzaromen) wie z.B. n-Butylphthalid oder Cineol, aber auch Aromastoffe mit arzneilicher Anwendung wie Eukalyptus- und Thymianöl, Methylsalicylat, Terpentinöl und Kamillenöl genannt.The above list is exemplary and can be supplemented by substances of the same function known to the person skilled in the art. Active components can be, for example, medicinal or cosmetic active ingredients, dietary additives to foods, dyes or diagnostics. In particular, the process according to the invention is applicable to the aroma substances which are otherwise difficult to process because of their volatility. Aromas which can be used with this invention are essentially essential oils (volatile, water-insoluble distillates from fragrant plant components) and other volatile, fragrant substances which have a limited miscibility with water. Examples include, for example, phenylethanol as a component of rose fragrances, menthol, eucalyptol (cineol), camphene and pinene in peppermint-like aromas, appetizing aroma substances (spice aromas) such as n-butyl phthalide or cineol, but also aroma substances with medicinal use such as eucalyptus - And called thyme oil, methyl salicylate, turpentine oil and chamomile oil.
Ein sehr weites Feld nehmen Essenzen und Aromen ein, die als Zusätze für Lebensmittel und in vorgefertigten Lebens- mittelzusatzstoffen im Einsatz sind. Hier seien beispielhaft die sogenannten Fruchtether genannt, aber auch andere Aromastoffe wie Ethylvanillin, 6-Methylcumarin, Citronellol oder auch Essigsäure-n-butyl-ester. Zusätze von oberflächenaktiven Substanzen können die Gleichmäßigkeit der Verteilung von Aromatröpfchen verbessern.Essences and flavors, which are used as additives for food and in pre-made food additives, occupy a very wide field. The so-called fruit ethers may be mentioned here by way of example, but also other flavorings such as ethylvanillin, 6-methylcoumarin, citronellol or also n-butyl acetate. Additions of surface-active substances can improve the uniformity of the distribution of aromatic droplets.
Es kann sich in besonderen Fällen als vorteilhaft erweisen, eine oder mehrere weitere Schichten gleicher oder unterschiedlicher Zusammensetzung aufzubringen, etwa um besondere Oberflächen- oder Zugeigenschaften zu erreichen.In special cases it can prove to be advantageous to apply one or more further layers of the same or different composition, for example in order to achieve special surface or tensile properties.
Die Masse wird zum Beispiel durch Einstreuen, Einkneten oder langsames Digerieren der festen Bestandteile im Lösungsmittel (in der Regel Wasser, aber auch z.B. Ethanol, Aceton und andere kompatible, physiologisch akzeptable Lösemittel und deren Gemische kommen zum Einsatz) erzeugt. In diese Phase werden, sofern rezepturmäßig enthalten, unter langsamen Rühren die vorgewogene Aromastoffmenge und andere flüssige, lipophile Zusatzstoffe hinzugeben. Es handelt sich im Interesse der Zielsetzung der Erfindung hinsichtlich einer gleichmäßigeren Beschaffenheit als sehr vorteilhaft erwiesen, die Masse vor Beschichtung über einen Schnellauflaufenden Homogenisator zu homogenisieren.The mass is obtained, for example, by sprinkling, kneading or slowly digesting the solid components in the solvent (usually water, but also, for example, ethanol, Acetone and other compatible, physiologically acceptable solvents and their mixtures are used). If contained in the recipe, the pre-weighed amount of flavoring and other liquid, lipophilic additives are added to this phase with slow stirring. In the interest of the objective of the invention, it has proven to be very advantageous with regard to a more uniform nature to homogenize the mass before coating via a high-speed homogenizer.
Im erfindungsgemäßen Prozeß wird die Masse durch Streich-, Rakel- oder Extrusionsverfahren auf ein Substrat beschichtet und in einem aus mindestens drei unabhängig temperierbaren Zonen bestehenden Trocknungskanal getrocknet. Das Substrat kann grundsätzlich aus dem Fachmann bekannten und weithin eingesetzten Substraten wie z.B. Polyethylen- terephthalat, Polyethylen, Polypropylen, Polycarbonat, Polyurethan bestehen. Zum Einsatz kommen auch Laminate dieser Stoffe mit anderen Polymeren, Papier, Glasfasern und sonstigen Strukturbildnern zur Erhöhung der Reißfestigkeit. Zur Regulierung der Oberflächenhaftung können Maßnahmen wie Siliconisierung, Fluorierung, Säurebehandlung oder Korona- Behandlung nützlich sein, bedürfen aber im einzelnen Fall einer Abklärung ihrer physiologischen Verträglichkeit für den jeweiligen Anwendungszweck.In the process according to the invention, the mass is coated onto a substrate by brushing, knife coating or extrusion processes and is dried in a drying channel consisting of at least three independently temperature-controlled zones. The substrate can in principle be made from substrates known to those skilled in the art and widely used, e.g. Polyethylene terephthalate, polyethylene, polypropylene, polycarbonate, polyurethane exist. Laminates of these materials with other polymers, paper, glass fibers and other structure formers are also used to increase the tear resistance. Measures such as siliconization, fluorination, acid treatment or corona treatment can be useful to regulate the surface adhesion, but in individual cases they need to be clarified as to their physiological compatibility for the respective application.
Besondere erfindungsgemäße Vorteile werden erreicht, wenn die der Beschichtungsmasse zugewandte Oberfläche keine glatte, sondern eine konturierte, mattierte, in jedem Fall oberflächenrauhe Kontur aufweist. Die Rauhtiefe kann im Bereich von 0,1 um bis ca. 10 um liegen, bevorzugt zwischen 0,5 und 3 um. Vorteilhaft sind in der mikroskopischen Feinstruktur rundliche Erhebungen, welche die Gleitreibung weiter verringern.Particular advantages according to the invention are achieved if the surface facing the coating composition does not have a smooth, but rather a contoured, matted, in any case rough surface contour. The roughness can be in the range from 0.1 µm to approximately 10 µm, preferably between 0.5 and 3 µm. Rounded elevations, which further reduce sliding friction, are advantageous in the microscopic fine structure.
Das erfindungsgemäße Ziel wird regelmäßig dann erreicht, wenn die Trocknung bei zunächst ansteigender, spätestens in der letzten Zone dann wieder um 10°C reduzierter Prozeßtemperatur verläuft .The aim of the invention is regularly achieved when the drying with initially increasing, at the latest in in the last zone then process temperature reduced by 10 ° C again.
Die Prozeßgeschwindigkeit ist vorteilhaft so einzustellen, daß ein Produkt mit einer Äquivalent-Luftfeuchte von 50-75% r.F., bevorzugt 60-68% r.F., erhalten wird.The process speed is advantageously set so that a product with an equivalent air humidity of 50-75% RH, preferably 60-68% RH, is obtained.
Die erhaltenen Produkte erwiesen sich unter diesen Prozeßbedingungen als flächenstabil, flexibel und bruchfest und weitgehend reißfest. Die entstandenen Oberflächen weisen so gut wie keinen "kalten Fluß" auf, sind also grundsätzlich formstabil. Die Folie läßt sich ohne merkliche Dehnung von der Unterlage abnehmen und separat weiterverarbeiten.Under these process conditions, the products obtained proved to be surface-stable, flexible and unbreakable and largely tear-resistant. The resulting surfaces have practically no "cold flow", so they are basically dimensionally stable. The film can be removed from the base without noticeable stretching and processed separately.
Die Äquivalent-Luftfeuchte wird folgendermaßen ermittelt: Ein frisch gefertigter Produktstreifen von ca. 0,1 ma Fläche wird mit Gummihandschuhen unmittelbar schnell gefaltet und in ein Weithals-Glasgefäß verbracht, dessen Deckel mit einer Durchbohrung so versehen ist, daß der Meßkopf eines Hygrometers eingeführt wird. Nach ca. einer Minute, je nach Gerätebauart, kann der Meßwert abgelesen werden.The equivalent air humidity is determined as follows: A freshly manufactured product strip of approx. 0.1 m a surface is quickly folded with rubber gloves and placed in a wide-necked glass vessel, the lid of which is drilled so that the measuring head of a hygrometer is inserted becomes. After approximately one minute, depending on the type of device, the measured value can be read off.
Die Weiterverarbeitung vollzieht sich nach Längsschnitt in Stanzeinrichtungen oder einfach durch Querschnitt . Die hergestellten folienförmigen Produkte weisen bevorzugt eine Dicke zwischen 20 und 300 um auf; ihre Größe kann vorteilhaft 0,5 bis 12 cm2 betragen. Die spätere Verpackung kann einzeln oder im Stapel beispielsweise in Siegelbeuteln oder Dosierspendern erfolgen. Further processing takes place after a longitudinal cut in punching devices or simply through a cross section. The film-shaped products produced preferably have a thickness between 20 and 300 μm; their size can advantageously be 0.5 to 12 cm 2 . The subsequent packaging can be done individually or in a stack, for example in sealed bags or dispensers.
Claims
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HK02100760.6A HK1039069A1 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| JP2000598143A JP2002536402A (en) | 1999-02-12 | 2000-01-31 | Method for producing sheet-form administration agent |
| CA002362756A CA2362756C (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| HU0202877A HUP0202877A2 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| NZ513465A NZ513465A (en) | 1999-02-12 | 2000-01-31 | Process for producing film-type dosage forms |
| IL14476700A IL144767A0 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| BRPI0009962-7A BR0009962B1 (en) | 1999-02-12 | 2000-01-31 | PROCESS FOR PRODUCTION OF BLADE FORMS FOR PRODUCT MINISTRY |
| AU31514/00A AU777898B2 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| MXPA01007867A MXPA01007867A (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms. |
| EP00909123A EP1150663A2 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
| IL144767A IL144767A (en) | 1999-02-12 | 2001-08-07 | Method for producing film-type dosage forms |
| NO20013892A NO20013892D0 (en) | 1999-02-12 | 2001-08-09 | Process for preparing foil-shaped administration forms |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19905801A DE19905801B4 (en) | 1999-02-12 | 1999-02-12 | Process for the preparation of film-shaped dosage forms |
| DE19905801.6 | 1999-02-12 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09913089 A-371-Of-International | 2001-08-27 | ||
| US10/314,549 Continuation US6800329B2 (en) | 1999-02-12 | 2002-12-09 | Method for producing film-type dosage |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2000047190A2 true WO2000047190A2 (en) | 2000-08-17 |
| WO2000047190A3 WO2000047190A3 (en) | 2000-12-14 |
Family
ID=7897244
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2000/000739 Ceased WO2000047190A2 (en) | 1999-02-12 | 2000-01-31 | Method for producing film-type dosage forms |
Country Status (22)
| Country | Link |
|---|---|
| EP (1) | EP1150663A2 (en) |
| JP (1) | JP2002536402A (en) |
| KR (1) | KR100620068B1 (en) |
| CN (1) | CN1147293C (en) |
| AR (1) | AR022580A1 (en) |
| AU (1) | AU777898B2 (en) |
| BR (1) | BR0009962B1 (en) |
| CA (1) | CA2362756C (en) |
| CZ (1) | CZ301872B6 (en) |
| DE (1) | DE19905801B4 (en) |
| HK (1) | HK1039069A1 (en) |
| HU (1) | HUP0202877A2 (en) |
| IL (2) | IL144767A0 (en) |
| MX (1) | MXPA01007867A (en) |
| NO (1) | NO20013892D0 (en) |
| NZ (1) | NZ513465A (en) |
| PL (1) | PL202678B1 (en) |
| RU (1) | RU2226389C2 (en) |
| TR (1) | TR200102056T2 (en) |
| TW (1) | TWI254725B (en) |
| WO (1) | WO2000047190A2 (en) |
| ZA (1) | ZA200106580B (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005513140A (en) * | 2001-12-11 | 2005-05-12 | セアプロ インク | Cereal β-glucan composition, preparation method and use thereof |
| US10568839B2 (en) | 2011-01-11 | 2020-02-25 | Capsugel Belgium Nv | Hard capsules |
| US11319566B2 (en) | 2017-04-14 | 2022-05-03 | Capsugel Belgium Nv | Process for making pullulan |
| US11576870B2 (en) | 2017-04-14 | 2023-02-14 | Capsugel Belgium Nv | Pullulan capsules |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10114509A1 (en) * | 2001-03-23 | 2002-10-02 | Haarmann & Reimer Gmbh | Production of encapsulated product fixed to surface, by applying mixture of film-forming polymer, core material (especially fragrance or aroma) and organic solvent to surface and drying |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6055039A (en) * | 1983-09-07 | 1985-03-29 | Mitsubishi Acetate Co Ltd | Water-soluble polysaccharide film |
| DE3333240A1 (en) * | 1983-09-12 | 1985-03-28 | Schering AG, 1000 Berlin und 4709 Bergkamen | MEDIUM FOR TRANSDERMAL APPLICATION OF MEDICINAL PRODUCTS |
| JPH0744940B2 (en) * | 1986-12-24 | 1995-05-17 | ライオン株式会社 | Base material for oral application |
| DE3827561C1 (en) * | 1988-08-13 | 1989-12-28 | Lts Lohmann Therapie-Systeme Gmbh & Co Kg, 5450 Neuwied, De | |
| US5360420A (en) * | 1990-01-23 | 1994-11-01 | The Procter & Gamble Company | Absorbent structures containing stiffened fibers and superabsorbent material |
| US5656297A (en) * | 1992-03-12 | 1997-08-12 | Alkermes Controlled Therapeutics, Incorporated | Modulated release from biocompatible polymers |
| DE19652257A1 (en) * | 1996-12-16 | 1998-06-18 | Lohmann Therapie Syst Lts | Individually dosed, film-like dosage form that quickly disintegrates on contact with liquid and contains active ingredients and especially flavorings |
-
1999
- 1999-02-12 DE DE19905801A patent/DE19905801B4/en not_active Expired - Fee Related
-
2000
- 2000-01-27 TW TW089101364A patent/TWI254725B/en not_active IP Right Cessation
- 2000-01-31 BR BRPI0009962-7A patent/BR0009962B1/en not_active IP Right Cessation
- 2000-01-31 RU RU2001118268/15A patent/RU2226389C2/en not_active IP Right Cessation
- 2000-01-31 IL IL14476700A patent/IL144767A0/en active IP Right Grant
- 2000-01-31 HU HU0202877A patent/HUP0202877A2/en unknown
- 2000-01-31 EP EP00909123A patent/EP1150663A2/en not_active Ceased
- 2000-01-31 MX MXPA01007867A patent/MXPA01007867A/en not_active IP Right Cessation
- 2000-01-31 CA CA002362756A patent/CA2362756C/en not_active Expired - Fee Related
- 2000-01-31 CN CNB008028656A patent/CN1147293C/en not_active Expired - Fee Related
- 2000-01-31 NZ NZ513465A patent/NZ513465A/en not_active IP Right Cessation
- 2000-01-31 HK HK02100760.6A patent/HK1039069A1/en unknown
- 2000-01-31 WO PCT/EP2000/000739 patent/WO2000047190A2/en not_active Ceased
- 2000-01-31 JP JP2000598143A patent/JP2002536402A/en active Pending
- 2000-01-31 AU AU31514/00A patent/AU777898B2/en not_active Ceased
- 2000-01-31 PL PL349857A patent/PL202678B1/en unknown
- 2000-01-31 TR TR2001/02056T patent/TR200102056T2/en unknown
- 2000-01-31 KR KR1020017010143A patent/KR100620068B1/en not_active Expired - Fee Related
- 2000-01-31 CZ CZ20012900A patent/CZ301872B6/en not_active IP Right Cessation
- 2000-02-11 AR ARP000100610A patent/AR022580A1/en active IP Right Grant
-
2001
- 2001-08-07 IL IL144767A patent/IL144767A/en not_active IP Right Cessation
- 2001-08-09 NO NO20013892A patent/NO20013892D0/en not_active Application Discontinuation
- 2001-08-10 ZA ZA200106580A patent/ZA200106580B/en unknown
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005513140A (en) * | 2001-12-11 | 2005-05-12 | セアプロ インク | Cereal β-glucan composition, preparation method and use thereof |
| US8632798B2 (en) | 2001-12-11 | 2014-01-21 | Ceapro Inc. | Cereal β glucan compositions, methods of preparation and uses thereof |
| US10568839B2 (en) | 2011-01-11 | 2020-02-25 | Capsugel Belgium Nv | Hard capsules |
| US11319566B2 (en) | 2017-04-14 | 2022-05-03 | Capsugel Belgium Nv | Process for making pullulan |
| US11576870B2 (en) | 2017-04-14 | 2023-02-14 | Capsugel Belgium Nv | Pullulan capsules |
| US11878079B2 (en) | 2017-04-14 | 2024-01-23 | Capsugel Belgium Nv | Pullulan capsules |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1336820A (en) | 2002-02-20 |
| AU777898B2 (en) | 2004-11-04 |
| CZ20012900A3 (en) | 2002-01-16 |
| CA2362756C (en) | 2009-11-24 |
| AR022580A1 (en) | 2002-09-04 |
| MXPA01007867A (en) | 2002-07-02 |
| ZA200106580B (en) | 2002-02-14 |
| NO20013892L (en) | 2001-08-09 |
| PL202678B1 (en) | 2009-07-31 |
| HK1039069A1 (en) | 2002-04-12 |
| EP1150663A2 (en) | 2001-11-07 |
| NZ513465A (en) | 2003-05-30 |
| JP2002536402A (en) | 2002-10-29 |
| RU2226389C2 (en) | 2004-04-10 |
| HUP0202877A2 (en) | 2003-03-28 |
| BR0009962B1 (en) | 2014-07-29 |
| CA2362756A1 (en) | 2000-08-17 |
| NO20013892D0 (en) | 2001-08-09 |
| KR20010102050A (en) | 2001-11-15 |
| PL349857A1 (en) | 2002-09-23 |
| IL144767A (en) | 2006-08-20 |
| IL144767A0 (en) | 2002-06-30 |
| CZ301872B6 (en) | 2010-07-14 |
| DE19905801A1 (en) | 2000-08-17 |
| BR0009962A (en) | 2002-04-16 |
| TR200102056T2 (en) | 2001-11-21 |
| WO2000047190A3 (en) | 2000-12-14 |
| TWI254725B (en) | 2006-05-11 |
| DE19905801B4 (en) | 2008-03-13 |
| KR100620068B1 (en) | 2006-09-05 |
| AU3151400A (en) | 2000-08-29 |
| CN1147293C (en) | 2004-04-28 |
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