材料科学
差示扫描量热法
扫描电子显微镜
傅里叶变换红外光谱
多孔性
粉末衍射
化学工程
接触角
复合材料
化学
结晶学
热力学
物理
工程类
作者
Jiu Wang,Shunfang Liu,Min-Mei Lin,Peihong Chen,Hee‐Gyeong Yi,Zhufen Lv,Yuanfen Liu
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2025-03-28
卷期号:17 (4): 435-435
标识
DOI:10.3390/pharmaceutics17040435
摘要
Background: 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. Methods: 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. Results: 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). Conclusions: Collectively, this finding demonstrates the feasibility of fabricating highly hydrophilic and non-distensible ODTs without disintegrants using powder-based 3D printing.
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