TECNOLOGÍAS DE PRODUCCIÓN FARMACÉUTICA

Ingredientes de las cápsulas de gelatina

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6491412

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Soft gelatin capsules are a dosed soft dosage form, which consists of a shell and a drug enclosed in it. Capsules can have different shapes (round, oval, oblong, etc.), different size, color and consistency of the filler. To obtain capsule shells, various film-forming high-molecular substances are used, which are capable of forming elastic films and are characterized by a certain mechanical strength. Gelatin is the most widely used by the modern pharmaceutical industry as a forming material, so most capsules produced in the industry* are gelatin capsules.

Estandarización de ungüentos en producción.

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6492006

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Intra-shop control of ointments is carried out at almost every stage of production and especially before packing the drug. The final conclusion on all indicators of the quality of finished products is given by the quality control department of the plant. In the conditions of industrial production, the test is carried out in accordance with the requirements of the general article of the State Pharmacopoeia (GF) for ointments, as well as the requirements included in the articles of the GF for individual names of ointments. The ointment is standardized in appearance, uniformity, content of medicinal substances, pH value, degree of dispersion of solid particles, colloidal stability and thermal stability. The company controls the appearance, smell and characteristic organoleptic properties (if any) of ointments and other…

Etapas de prensado para materiales en polvo

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6492826

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The whole pressing process is proposed to be divided into three stages: compaction (pre-pressing); formation of a compact body; volumetric compression of the resulting compact body. At the first stage of pressing, under the influence of an external force, the material particles converge and seal due to their displacement relative to each other and filling voids. The forces overcome in this case are insignificant, the seal becomes noticeable even at low pressures. The applied energy is mainly spent on overcoming internal (between particles) and external (between particles and matrix machines) friction.

Granulación en seco de polvos

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6492990

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Dry granulation is a method in which a powdery material (a mixture of medicinal and auxiliary substances) is compacted to produce a granulate. Dry granulation is used in cases where wet granulation affects the stability and/or physico-chemical characteristics of the medicinal substance, as well as when the medicinal and auxiliary substances are poorly compressed after the wet granulation process. If medicinal substances undergo physical changes during drying (melting, softening, color change) or enter into chemical reactions, they are briquetted, i.e. briquettes are pressed from the powder on special briquetting presses with large matrices (25x25 mm) under high pressure.

Aglutinantes para granulación húmeda

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6492986

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There are some requirements for the granulating liquid, one of them is that the granulating liquid should not dissolve the active substance. Water, an aqueous solution of ethanol, acetone and methylene chloride can be used as a granulating liquid. A wide range of substances are used as binding agents for wet granulation in modern pharmaceutical production, for example: starch (5-15% g/g), starch derivatives, cellulose derivatives that improve the plasticity of granules, as well as gelatin (1-3% g/ g) and PVP (3-10% g/ g). The most common and effective binder for wet granulation in the modern pharmaceutical industry is a synthetic polymer such as Collidone (PVP), various brands of which (Collidone 25, 30 and 90F) are widely represented on the market.

Etapas de preparación de materias primas para la producción de tabletas

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6492402

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For most chemical and pharmaceutical preparations, the technology of tablet production consists of the following disparate operations of weighing the starting material, grinding, sieving, mixing, granulation, tableting (pressing), coating. Some of the listed operations in the manufacture of pharmaceuticals may be absent. Three common technological schemes for obtaining tablets are most common: using wet granulation, dry granulation and direct pressing.

Estandarización de supositorios en la industria farmacéutica.

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6492814

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All manufactured suppositories must meet the requirements of the State Pharmacopoeia XI: Suppositories must have a homogeneous mass. The uniformity of the suppository is checked visually on the longitudinal section by the presence or absence of inclusions, pieces of the "base, particles of various colors, other inclusions; at the same time, the presence of an air rod is permissible. Deviations in the mass of suppositories are allowed within 5%. Suppositories must have the correct uniform shape. In suppositories, medicinal substances must be precisely dosed. Suppositories should have a hardness that ensures ease of use.

Fuerza para empujar las tabletas fuera de la matriz

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6492403

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To push the compressed tablet out of the matrix, it is required to expend force to overcome friction and adhesion between the side surface of the tablet and the wall of the matrix. Taking into account the magnitude of the ejection force, additives of antifriction (sliding or lubricating) substances are predicted. As an example, the results of determining the technological characteristics of round-shaped substances are given. Powders with rounded particles with a basic particle size of more than 100 microns (ranitidine g/cl, carbamazepine, phenazepam) have high (8-9 g/s) flowability, high volume density before and after compaction, but insignificant compressibility and a small compaction coefficient. Phenazepam has a slightly lower flowability value (8 g/s), probably because it contains more small fractions and does not contain particles...

Bases para supositorios y sus requisitos

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6492817

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From a physico-chemical point of view, suppositories are considered as dispersed systems consisting of a dispersion medium, represented by the basis of the Dispersed phase, in the role of which medicinal substances act. Depending on the properties of medicinal substances, dispersed systems of suppositories can be either homogeneous or heterogeneous. Homogeneous systems are formed when the medicinal substance is dissolved in the base. Heterogeneous systems are formed in the case of the introduction of medecine into the base by the type of emulsion or suspension. In the structure of suppositories, there are basic (medicinal substances) and auxiliary (carriers or base) components. There are a number of requirements for suppository bases: the bases must maintain sufficient hardness at room temperature; the melting (dissolution) temperature of the...

Prensado de comprimidos en la producción farmacéutica

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6492823

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Tableting (pressing) is the process of forming tablets from granular or powdery material under pressure. In modern pharmaceutical production, tableting is carried out on special presses called tablet machines.