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Film coatings of tablets

  • Film coating for tablets
  • Application of film coatings on tablets
  • Application of a film coating on tablets
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Film coatings of tablets

Film coating is a thin shell formed on the surface of a microsphere (pellet). Tablets or pellets after drying of the film-forming agent solution applied to their surface. The thickness of the film coating layer is from about 5 to about 50 microns. Droplets of coating fluid are sprayed onto the initial particles. The supplied process air vaporizes the liquid and dries the film layer on the surface of the particles.
The small droplet size and low viscosity ensure uniform distribution of the film on the particle surface. An important consideration in coating is to apply the coating material very uniformly. Coatings should be dense, free of mechanical damage and cracks. Film coating is an effective way of applying protective films to influence particle properties. Initially, film coating technology was based on the use of polymers soluble in organic solvents, which have disadvantages such as ignition hazards, toxicity, pollution problems, and cost. However, since the advent of film coatings, there have been significant changes in coating process technology and equipment to enable the application of new coatings. Film coatings, depending on their solubility, are usually divided into: water-soluble, gastric juice soluble, enteric soluble and insoluble.

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  • Information updated : 09 / 11 / 2024
  • In stock
  • Manufacturer : 1 year for Film coatings of tablets

Model: Film coatings of tablets

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Insoluble coatings include ethylcellulose, surfactants, etc. These coatings are created with the help of some cellulose derivatives, which are applied to the tablet in the form of solutions. To increase the strength and elasticity of the coatings, plasticizers are introduced into their composition. The mechanism of drug release from tablets with insoluble shells is that digestive juices can quickly penetrate through the pores of the shell and dissolve the active substance of the tablet or cause its swelling. In the first case, the dissolved substance diffuses through the film in the opposite direction – towards the gastrointestinal tract under the influence of the concentration difference, in the second case – there is a rupture of the shell by increasing the volume of the tablet, after which the drug is released in the usual way. Uniform release of the drug substance through the intact shell occurs regardless of the composition, enzyme action and pH value of the environment in the gastrointestinal tract. It depends only on the solubility and pore size of the shell, which can be modified as required. Therefore, it is possible to produce tablets with a pre-calculated rate of drug release.

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Technical specifications

Water-soluble coatings improve the appearance of tablets, correct their taste and odor, protect from mechanical damage, but do not protect from air moisture. Water-soluble coatings are formed by PVP, MC, Na CMC, etc., applied to tablets in the form of water-ethanol or aqueous solutions. Coatings soluble in gastric juice – films protecting from moisture, provide rapid dissolution in the stomach (within 10-30 min). The film-formers of this group include polymers having amino groups in the molecule – diethylaminomethylcellulose, para-aminotenzoates of sugars and acetyl-cellulose. Coating of tablets is carried out by solutions of the above substances in organic solvents – ethanol or isopropanol, which are volatilized during coating and drying. Intestine-soluble coatings protect the drug substance contained in the tablet from the acid reaction of gastric juice, protect the gastric mucosa from the irritating effect of some drugs, localize the drug substance in the intestine, prolonging to a certain extent its effect, and also have a pronounced moisture-protective effect. The process of dissolution of shells in the body is due to the effect on them a complex of enzymes to various solubilizing substances contained in the intestinal juice.

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Additional information

High molecular weight compounds are used as film formers for intestine-soluble coatings. They dissociate in neutral and alkaline media to form insoluble salts. Both natural substances are used: shellac, casein, keratin, paraffin, ceresin, cetyl alcohol, and synthetic products: stearic acid in combination of fats with bile acids, butyl stearate, acetylphthalyl cellulose, poly-vinyl acetateflatate, polyacrylic resins (Eudragid). The listed film formers are applied to tablets in the form of solutions. Pigments and dyes are added to the solutions to obtain colored shells. By varying different polymers and different film thicknesses, it is possible to achieve disintegration of the tablet in a certain part of the intestinal tract. Intestine-soluble coatings can withstand the effects of gastric juice for 2-4 h or more, which allows such dosage forms to pass through the stomach unchanged; in the intestinal juice they disintegrate within 1 h, ensuring the release of the drug in the intestine. Insoluble coatings are films with a microporous structure for controlled release of the drug substance. The main purpose of this type of coatings is to protect tablets, pellets or granules from mechanical damage and atmospheric moisture, to eliminate unpleasant odor and taste of the medicinal substance, prolonging its effect.

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