AI Article Synopsis

  • This study examines how mucoadhesive polymers can enhance the controlled release of poorly water-soluble drugs in tablet form.
  • The researchers used prednisolone and zein in the core tablets, testing Carbopol 940 and hydroxypropyl methylcellulose (HPMC) as the mucoadhesive polymers for sustained release.
  • Results show that HPMC is effective for drug release control due to its ability to absorb water and create pores in the coating, facilitating a gradual drug release suitable for targeting the colon.

Article Abstract

Background: The mucoadhesive polymers play an important role in targeted and controlled drug delivery.

Objectives: This study aimed to investigate the drug release behaviour and interpret the role of mucoadhesive polymers involved in the coating layer of mucoadhesive tablets for the sustained release of a poorly water-soluble drug.

Methods: A solid dispersion of prednisolone and zein was used in the core tablets created with two mucoadhesive polymers, which included Carbopol 940 and hydroxypropyl methylcellulose K4M. In addition, the properties of a single-layer coating, created from the combination of zein and Kollicoat MAE 100P to delay release through the upper parts of the gastrointestinal tract, were investigated in the presence of the above mucoadhesive polymers; these properties included drug dissolution, mucoadhesion, surface morphology, swelling and erosion.

Results: The mucoadhesive polymer concentrations and types were integrated not only into the core tablets through a swelling/erosion mechanism but also into the surface polymer coatings for controlled drug release. HPMC was preferred in the formulations due to the ability to form pores on the surface coating, allowing water uptake so that the coating could control drug release for a later stage via a swelling/erosion mechanism.

Conclusion: The proposed mechanism determined in this project could be beneficial in the selection of polymers for applications targeting the colon with coated mucoadhesive tablets. Graphical abstract.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7704813PMC
http://dx.doi.org/10.1007/s40199-020-00360-xDOI Listing

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