4.7 Article

Preparation and advanced characterization of highly drug-loaded, 3D printed orodispersible tablets containing fluconazole

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 630, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2022.122444

Keywords

Fused deposition modeling; Orodispersible tablets; Stability; High drug loading; Hot -melt extrusion; Surface dissolution imaging

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Due to the versatility of 3D printing in designing spatial structures, it can be applied to customized medicine production. However, further optimization and development of quality verification mechanisms are required for using this method in dosage form production. In this study, the authors prepared and characterized 3D printed oro-dispersible tablets containing fluconazole using FDM. The tablets showed good quality, precision, and met the required criteria for ODTs according to the European Pharmacopeia. The stability of the formulation was also confirmed.
Due to the possibility of designing various spatial structures, three-dimensional printing can be implemented in the production of customized medicines. Nevertheless, the use of these methods for the production of dosage forms requires further optimization, understanding, and development of printouts' quality verification mecha-nisms. Therefore, the goal of our work was the preparation and advanced characterization of 3D printed oro-dispersible tablets (ODTs) containing fluconazole, printed by the fused deposition modeling (FDM) method.We prepared and analyzed 7 printable filaments containing from 10% to 70% fluconazole, used as model API. Obtaining a FDM-printable filament with such a high API content makes our work unique. In addition, we confirmed the 12-month stability of the formulation, which, to our knowledge, is the first study of this type.Next, we printed 10 series of porous tablets containing 50 mg of API from both fresh and stored filaments containing 20 %, 40 %, or 70 % fluconazole. We confirmed the high quality and precision of the printouts using scanning electron microscopy. The detailed analysis of the tablets' disintegration process included the Phar-macopeial test, but also the surface dissolution imaging analysis (SDI) and the test simulating oral conditions performed in own-constructed apparatus.For each composition, we obtained tablets disintegrating in less than 3 min, i.e., meeting the criteria for ODTs required by the European Pharmacopeia. The filaments' storage at ambient conditions did not affect the quality of the tablets. All printed tablets released over 95% of the fluconazole within 30 min. Moreover, the printouts were stable for two weeks.

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