Περίληψη:
Background: Mesalazine (5-aminosalicylic acid, 5-ASA) is a drug substance with an anti-inflammatory activity, which is mainly used in the symptomatic treatment of diseases, such as Ulcerative Colitis, the Crohn's disease and the idiopathic inflammatory bowel disease. Mesalazine exerts its effect locally in the inflamed area of the intestine and not through systematic absorption, therefore the investigation of its release characteristics from solid pharmaceutical formulations is of great importance. Objective: The development of novel mesalazine modified release formulations with improved properties, regarding drug release in the gastrointestinal tract, by utilisation of the Design of Experiments (DoE) approach. Methods: D-optimal experimental design was applied. A Simplex Lattice mixture design was used for the development of suitable capsules containing 4 mini tablets and a D-optimal mixture design was used for compression-coated tablets, with the following characteristics: ≤10% release in 2 h, to minimize its degradation in the upper gastrointestinal tract, 20-40% release in 5 h for mesalazine administration in the small intestine, and quantitative release in 12 h for colonic delivery. The dissolution experiments were conducted in gastrointestinal-like fluids and pectinases to simulate the pectinolytic enzymes present in the colon. Results: The optimal compositions were reached via the desirability function, as a compromise to the different responses. The optimal solutions for both formulations led to colon-specific delivery of the active substance with minimal 5-ASA release in the upper gastrointestinal tract and appeared to conform with the pre-determined characteristics. Hard gelatin capsules, when filled with mini-tablets led to the aimed modified release profile, having sigmoidal characteristics and compression coated tablets led to colonic delivery. Conclusion: Two novel mesalazine formulations were developed with the desirable colonic release, by conducting a minimal number of experiments, as suggested by DoE experimental design. © 2020 Bentham Science Publishers.
Συγγραφείς:
Vlachou, M.
Siamidi, A.
Dotsikas, Y.
Λέξεις-κλειδιά:
esterase; gelatin; mesalazine; pectin; pectin lyase; polygalacturonase; xanthan, Article; drug coating; drug degradation; drug release; drug solubility; experimental design; gastrointestinal tract; in vitro study; large intestine; microcapsule; priority journal; process optimization; small intestine; tablet compression; tablet formulation; tablet friability; tablet hardness; tablet thickness; upper gastrointestinal tract
