polyvinylacetate phthalate polymer

polyvinylacetate phthalate polymer Chemische Eigenschaften,Einsatz,Produktion Methoden

• Chemische Eigenschaften

  Polyvinyl acetate phthalate is a free-flowing white to off-white powder and may have a slight odor of acetic acid. The material is essentially amorphous.

• Vorbereitung Methode

  Polyvinyl acetate phthalate is a reaction product of phthalic anhydride, sodium acetate, and a partially hydrolyzed polyvinyl alcohol. The polyvinyl alcohol is a low molecular weight grade, and 87–89 mole percent is hydrolyzed. Therefore, the polyvinyl acetate phthalate polymer is a partial esterification of a partially hydrolyzed polyvinyl acetate.

• Pharmazeutische Anwendungen

  Polyvinyl acetate phthalate is a viscosity-modifying agent that is used in pharmaceutical formulations to produce enteric coatings for products and for the core sealing of tablets prior to a sugar-coating process. Polyvinyl acetate phthalate does not exhibit tackiness during coating and produces strong robust films.
  Plasticizers are often included in polyvinyl acetate phthalate coating formulations to enable a continuous, homogeneous, noncracking film to be produced. Polyvinyl acetate phthalate has been shown to be compatible with several plasticizers such as glyceryl triacetate, triethyl citrate, acetyl triethylcitrate, diethyl phthalate and polyethylene glycol 400. For enteric coating applications, polyvinyl acetate phthalate is dissolved in a solvent system together with other additives such as diethyl phthalate and stearic acid. Methanol may be used as the solvent if a colorless film is required; for a colored film, methanol or ethanol/water may be used depending on the amount of pigment to be incorporated. A weight increase of up to 8% is necessary for nonpigmented systems, whereas for pigmented systems a weight increase of 6% is usually required. A formulated, aqueous-based coating solution ( Sureteric, Colorcon) is available commercially for the enteric coating of tablets, hard and soft gelatin capsules and granules. More recently, hot-melt extrusion of coating polymers, such as polyvinyl acetate phthalate, has been described for the enteric coating of capsules.
  Polyvinyl acetate phthalate has superseded materials such as shellac in producing the initial layers of coating (the sealing coat) in the sugar coating process for tablets. The sealing coating should be kept as thin as possible while providing an adequate barrier to moisture, a balance that is often difficult to achieve in practice. A solvent system containing a high proportion of industrial methylated spirits and other additives can be used. Two coats are usually sufficient to seal most tablets, although up to five may be necessary for tablets containing alkaline ingredients. If an enteric coating is also required, between six and 12 coats may be necessary;
  The properties of polyvinyl acetate phthalate enteric coating have been compared with those of other enteric polymers such as cellulose acetate phthalate and Eudragit L 30D.The factors that affect the release kinetics from polyvinyl acetate phthalate enteric-coated tablets have also been described.A method for enteric coating hypromellose capsules which avoids the sealing step prior to coating has been developed. The properties of several enteric coating polymers, including polyvinyl acetate phthalate, were assessed.

• Sicherheit(Safety)

  Polyvinyl acetate phthalate is used in oral pharmaceutical formulations and is generally regarded as an essentially nonirritant and nontoxic material when used as an excipient.

• Lager

  Polyvinyl acetate phthalate should be stored in airtight containers. It is relatively stable to temperature and humidity, and does not age, giving predictable release profiles even after prolonged storage.
  At high temperature and humidity, polyvinyl acetate phthalate undergoes less hydrolysis than other commonly used enteric coating polymers. In aqueous colloidal dispersions of polyvinyl acetate phthalate, the formation of free phthalic acid through hydrolysis was found to adversely affect physical stability.
  Following storage at room temperature for 9 months, capsules coated with a commercial polyvinyl acetate phthalate formulation (Coateric) were found to retain gastroresistant properties and showed no apparent physical change; however, a delayed drug dissolution profile was observed after storage. Storage at 37°C, or 37°C and 80% relative humidity, for 3 months resulted in capsules having an unsatisfactory appearance.

• Inkompatibilitäten

  Polyvinyl acetate phthalate reacts with povidone to form an insoluble complex that precipitates out of solution;benzocaine is also incompatible with polyvinyl acetate phthalate.Erythromycin disperses in polyvinyl acetate phthalate and has been shown to be physically stable while omeprazole exists in the amorphous form in polyvinyl acetate phthalate coatings with no evidence of interaction.

• Regulatory Status

  Included in the FDA Inactive Ingredients Database (sustainedaction oral tablet). Included in nonparenteral medicines (enteric coated tablets; in printing ink formulations used for oral tablets and capsules) licensed in Europe. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

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