Fabricating Oral Disintegrating Tablets Without Disintegrant Using Powder-Based 3D Printing
<b>Background</b>: Powder-based 3D printing, an advanced additive manufacturing technique, can produce oral disintegrating tablets (ODTs) without disintegrants, creating larger-pored tablets via layer-by-layer powder stacking for better water absorption than traditional tablets. <b>Methods</b>: This study focused on using powder-based 3D printing to fabricate clozapine-based ODTs. Through central composite design (CCD), the formulation of ODTs was optimized for rapid disintegration. Analytical techniques such as X-ray Powder Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and Differential Scanning Calorimetry (DSC) were employed to investigate the compatibility between clozapine and excipients. <b>Results</b>: The optimized 3D-printed ODTs exhibited a remarkably short disintegration time of (9.9 ± 0.7) s compared to (40) s for compressed tablets. The contact angle of the 3D-printed ODTs was measured as 60.48 ± 0.36°, indicating favorable wettability for disintegration. Scanning Electron Microscopy (SEM) analysis revealed a porous structure in 3D-printed tablets, with a porosity of 48.97% (over two times higher than that of compressed tablets as determined by mercury injection meter). <b>Conclusions</b>: Collectively, this finding demonstrates the feasibility of fabricating highly hydrophilic and non-distensible ODTs without disintegrants using powder-based 3D printing.
Authors
- Yuanfen Liu
- Hee‐Gyeong Yi (ORCID: https://orcid.org/0000-0002-3042-8564)
- Shunfang Liu (ORCID: https://orcid.org/0009-0007-3178-5196)
- Jiu Wang (ORCID: https://orcid.org/0009-0005-8594-3706)
- Min-Mei Lin
- Zhufen Lv
- Peihong Chen (ORCID: https://orcid.org/0000-0003-1094-1560)
Institutions
- Guangdong Pharmaceutical University (CN)
- People 's Hospital of Jilin Province (CN)
- Jiangsu Vocational College of Medicine (CN)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2025-03-28
- DOI
- https://doi.org/10.3390/pharmaceutics17040435
- Citations
- 1
- Primary Topic
- Drug Solubulity and Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.79