Development of mesalazine pellets coated with methacrylic-derived polymer

Authors

  • Simone Cristina Déo Federal University of Paraná; Pharmacy Department
  • Itamar Francisco Andreazza Federal University of Paraná; Pharmacy Department
  • João Carlos Possamai Federal University of Paraná; Plant Science and Plant Health Department

DOI:

https://doi.org/10.1590/S1984-82502011000100013

Keywords:

Mesalazine, Coated pellets^i1^sevaluat, Coated pellets^i1^sdissolution prof, Extrusion- Spheronisation^i1^spellets obtent, Drugs^i1^smodified rele

Abstract

Mesalazine (5-ASA) is the standard drug for the treatment of inflammatory bowel disease (IBD) due to its local effect on intestinal and colonic mucosa. The effective and safe treatment of this disease requires more efficient delivery of the active substance to its site of action. The focus of this study was the use of multiparticulate systems, a modified release form in which the drug is divided into several functional subunits of release in the form of granules or pellets. When these forms are administered, they are rapidly disintegrated, distributing their content throughout the gastrointestinal tract. The aim of this study was to develop and evaluate a multiparticulate system consisting of pellets coated with polymer for pH-dependent release, derived from methacrylic acid and incorporated into the tablet dosage form of mesalazine as a model drug. The extrusion-spheronisation technique was used, resulting in smooth and spherical pellets with uniform size distribution, which were coated in fluidized bed using Opadry® Enteric 94K28327 containing Eudragit® S100 as the agent regulating drug release. The dissolution profile of coated pellets showed good control of drug release from the polymer at the two levels of coating evaluated (8% and 10%), but only the 10% coated pellets were statistically similar to Asalit® 400 mg.

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Published

2011-03-01

Issue

Section

Articles

How to Cite

Development of mesalazine pellets coated with methacrylic-derived polymer . (2011). Brazilian Journal of Pharmaceutical Sciences, 47(1), 103-109. https://doi.org/10.1590/S1984-82502011000100013