UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
AAPS PharmSciTech. 2018 Nov;19(8):3355-3361. doi: 10.1208/s12249-018-1075-3. Epub 2018 Jun 8.
Additive manufacturing (3D printing) permits the fabrication of tablets in shapes unattainable by powder compaction, and so the effects of geometry on drug release behavior is easily assessed. Here, tablets (printlets) comprising of paracetamol dispersed in polyethylene glycol were printed using stereolithographic 3D printing. A number of geometric shapes were produced (cube, disc, pyramid, sphere and torus) with either constant surface area (SA) or constant surface area/volume ratio (SA/V). Dissolution testing showed that printlets with constant SA/V ratio released drug at the same rate, while those with constant SA released drug at different rates. A series of tori with increasing SA/V ratio (from 0.5 to 2.4) were printed, and it was found that dissolution rate increased as the SA/V ratio increased. The data show that printlets can be fabricated in multiple shapes and that dissolution performance can be maintained if the SA/V ratio is constant or that dissolution performance of printlets can be fine-tuned by varying SA/V ratio. The results suggest that 3D printing is therefore a suitable manufacturing method for personalized dosage forms.
增材制造(3D 打印)可以制造出通过粉末压实无法实现的片剂形状,因此很容易评估几何形状对药物释放行为的影响。在这里,使用立体光刻 3D 打印技术打印了包含聚乙二醇分散的扑热息痛的片剂(打印片)。制作了许多具有恒定表面积(SA)或恒定表面积/体积比(SA/V)的几何形状(立方体、圆盘、金字塔、球体和圆环)。溶解试验表明,具有恒定 SA/V 比的打印片以相同的速度释放药物,而具有恒定 SA 的打印片则以不同的速度释放药物。打印了一系列具有递增 SA/V 比(从 0.5 到 2.4)的圆环,发现随着 SA/V 比的增加,溶解速率增加。数据表明,如果保持 SA/V 比不变,可以制造出多种形状的打印片并保持溶解性能,或者可以通过改变 SA/V 比来微调打印片的溶解性能。结果表明,因此 3D 打印是一种适合个性化剂型制造的方法。