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Inkjet-printed Polyvinyl Alcohol Multilayers
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Polyvinyl acetate-based film coatings.

K Kolter1, A Dashevsky, Muhamad Irfan

  • 1BASF SE, Development Pharma Ingredients, Ludwigshafen, Germany.

International Journal of Pharmaceutics
|October 1, 2013
PubMed
Summary

Polyvinyl acetate (Kollicoat® SR 30 D) offers pH-independent controlled drug release coatings. Its properties allow easy processing and adjustable drug release, presenting a novel alternative to OROS systems.

Keywords:
Aqueous colloidal polymer dispersionsCompaction of pelletsCuringExtended releaseKollicoat(®) SR 30 DOROS

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Area of Science:

  • Pharmaceutical technology
  • Materials science

Background:

  • Kollicoat® SR 30 D is a polyvinyl acetate-based polymer dispersion used for controlled drug release coatings.
  • It exhibits moderate swelling, lipophilicity, and pH-independent permeability, along with high flexibility.
  • Its low minimum film forming temperature (MFT) of 18°C facilitates processing without plasticizers.

Purpose of the Study:

  • To evaluate Kollicoat® SR 30 D for controlled release coating applications.
  • To investigate the influence of formulation variables on drug release profiles.
  • To explore its potential as an alternative to osmotic drug delivery systems.

Main Methods:

  • Coating of pellets with Kollicoat® SR 30 D.
  • Assessment of film properties including swelling, lipophilicity, and flexibility.
  • Drug release studies under various conditions (pH, coating level, excipients).
  • Evaluation of plasticizer and pore-former effects on film and release characteristics.

Main Results:

  • Kollicoat® SR 30 D coatings demonstrated pH-independent drug release.
  • Drug release was controllable via coating level and addition of pore-forming polymers (Kollidon® 30, Kollicoat® IR).
  • Addition of triethyl citrate improved film flexibility and allowed for tablet compaction with minimal impact on drug release.

Conclusions:

  • Kollicoat® SR 30 D is a versatile polymer for developing controlled-release dosage forms with pH-independent drug release.
  • Formulation adjustments, including plasticizers and pore formers, effectively modulate drug release kinetics.
  • Combinations with Kollicoat® IR offer a promising, drill-free alternative to OROS systems for controlled drug delivery.