Abstract:
PROBLEM TO BE SOLVED: To obtain an administration form producible by melt extrusion, capable of rapidly releasing an action substance, by using a homopolymer and copolymer of N-vinylcaprolactam as a polymer binder. SOLUTION: A homopolymer of N-vinyl caprolactam or a copolymer containing preferably at least 10 wt.% of N-vinylcaprolactam unit by copolymerization as a polymer binder is formulated with at least one action substance and optionally an common additive. A plastic mixture is formed and molded to give the objective solid administration form.
Abstract:
PROBLEM TO BE SOLVED: To produce the subject dosage form producible by melt extrusion and capable of slowly releasing an agent by using a water swellable graft copolymer as a high-molecular weight binder. SOLUTION: When (A) at least one kind of a high-molecular weight binder, (B) at least one kind of agent and, as necessary, (C) a usual additive are mixed and formed under the formation of a plastic mixture, a water swellable graft copolymer or a mixture thereof is used as the ingredient A. The amounts of the formulated ingredients A and B based on the total weight of the dosage form are preferably 10-100 wt.%, more preferably 40-99.9 wt.% of the ingredient A and preferably 0-90 wt.%, more preferably 0.1-60 wt.% of the ingredient B.
Abstract:
PROBLEM TO BE SOLVED: To produce a novel creatine containing solid administration by a melt calendering. SOLUTION: This creatine-containing solid administration form is produced by (a) preparing a mixture containing at least one of high-molecular weight binders having thermoplastic physiologically permissible water-solubility or water-swelling property, creatine and water of 1-20 mol based on 1 mol of creatine, (b) plasticizing this mixture at the softening point of the high-molecular weight binders or over this softening point and (c) molding the plasticized mixture to the administration form and cooling.
Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing a solid dosage form by extruding a melted product containing a specific polyamide as a binder, capable of simply obtaining the dosage form having an active ingredient sustained release property at an advantageous cost. SOLUTION: This method for producing a dosage form comprises mixing (A) at least one of polymer binder, if necessary, with (B) at least one kind of active ingredient and, if necessary, further with (C) one or more kinds of conventional additives and subsequently molding the formed plastic mixture. Therein, a polyamide having sulfonate groups is used as the component A. The polyamide is preferably obtained from (i) 0-90 mol.% of at least one kind of monoaminocarboxylic acid, its lactam or a mixture of the monoaminocarboxylic acid with its lactam, (ii) 5-50 mol.% of at least one kind of a primary or secondary diamine and (iii) 0.5-49.5 mol.% of at least one kind of sulfonate group-having dicarboxylic acid.
Abstract:
PROBLEM TO BE SOLVED: To develop a method for inexpensively and simply preparing a functional substance-containing preparation which is dissolved or itself dispersed in water or in gastrointestinal tracts, such as medicines or food additives. SOLUTION: This method for preparing granules which contain a biologically active substance and in which the biologically active substance is homogeneously dispersed in a matrix based on at least one thermoplastic polymer having a solubility dependent to pH values in an aqueous medium, by homogeneously mixing the charged substance in the state of the melt and then extruding and shaping the mixture, characterized by forming the granules in an insoluble or nondispersible cooling medium.
Abstract:
PROBLEM TO BE SOLVED: To obtain a solubilizing agent having a sufficient solubility and high solubilizing activities in water, and capable of being applied to medicines, cosmetics and foods. SOLUTION: This use is the one of copolymers comprising (a) 82-99.9 mol.% of at least one monoethylenically unsaturated a 3-8C carboxylic acid, (b) 0.1-18 mol.% of at least one monomer selected from the group of (b1 ) N-(8-30C alkyl)- substituted amides of monoethylenically unsaturated 3-8C carboxylic acids, (b2 ) N,N-(8-30C dialkyl)-substituted amides of monoethylenically unsaturated 3-8C carboxylic acids and (b3 ) 8-30C alkyl esters of monoethylenically unsaturated 3-8C carboxylic acids, and (c) 0-17.9 mol.% of at least one monomer selected from the group of (c1 ) vinyl esters of aliphatic 8-30C carboxylic acids and (c2 ) 8-30C alkylvinyl ethers, in which the mol.% data for the individual components adding up to 100%, as a solubilizer.
Abstract:
The invention relates to a solid preparation, containing an acid-sensitive proton-pump blocker as the active substance, whereby said active substance is present in an x-ray amorphous form and is embedded in molecularly dispersed form in an auxiliary agent matrix.
Abstract:
The invention relates to a method for producing solid, spherical forms containing at least one pharmaceutical active agent homogeneously dispersed in an auxiliary matrix. According to this method, the constituents are mixed to form a melt which is then shaped. The invention is characterised in that at least one pharmaceutical active agent is processed with at least one thermoplastically processable matrix auxiliary to form a homogeneous melt with a viscosity of less than 5000 mPas and in that this melt is shaped into drops using a rotating perforated roll. These drops are then cooled so that they solidify.
Abstract:
The invention relates to self-emulsifying formulations based on an active substance constituent and on a formulation base with a lipid constituent and with a binding agent constituent. The invention also relates to the use of this formulation as a dosed form in the area of life science. The invention also relates to a method for producing self-emulsifying formulations by mixing the formulation constituents while forming a plastic mixture and optionally while preparing the formulations as a dosed form, advantageously while using melt extrusion. The formulations spontaneously form emulsions in water or in aqueous fluids.
Abstract:
The invention relates to solid pharmaceutical galenic forms comprising an agent in the form of a physical mixture of two different preparations with regard to the physical state of the agent.