Qian Haonan, Chen Di, Xu Xiangyu, Li Rui, Yan Guangrong, Fan Tianyuan
The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
School Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Pharmaceutics. 2022 Jan 25;14(2):281. doi: 10.3390/pharmaceutics14020281.
The aim of this work was to design and fabricate fused deposition modeling (FDM) 3D-printed sustained-release gastric-floating formulations with different shapes (cylinder, capsule and hemisphere) and infill percentages (0% and 15%), and to investigate the influence of shape and infill percentage on the properties of the printed formulations. Drug-loaded filaments containing HPMC, Soluplus and verapamil hydrochloride were prepared via hot-melt extrusion (HME) and then used to print the following gastric-floating formulations: cylinder-15, capsule-0, capsule-15, hemisphere-0 and hemisphere-15. The morphology of the filaments and the printed formulations were observed by scanning electron microscopy (SEM). The physical state of the drugs in the filaments and the printed formulations were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The printed formulations were evaluated in vitro, including the weight variation, hardness, floating time, drug content and drug release. The results showed that the drug-loaded filament prepared was successful in printing the gastric floating formulations. Verapamil hydrochloride was proved thermally stable during HME and FDM, and in an amorphous state in the filament and the printed formulations. The shape and infill percentage of the printed formulations effected the hardness, floating time and in vitro drug release.
本研究旨在设计并制造具有不同形状(圆柱体、胶囊和半球体)和填充率(0%和15%)的熔融沉积建模(FDM)3D打印缓释胃漂浮制剂,并研究形状和填充率对打印制剂性能的影响。通过热熔挤出(HME)制备含羟丙基甲基纤维素(HPMC)、固体分散体(Soluplus)和盐酸维拉帕米的载药长丝,然后用于打印以下胃漂浮制剂:圆柱体-15、胶囊-0、胶囊-15、半球体-0和半球体-15。通过扫描电子显微镜(SEM)观察长丝和打印制剂的形态。通过X射线衍射(XRD)、热重分析(TGA)和差示扫描量热法(DSC)对长丝和打印制剂中药物的物理状态进行表征。对打印制剂进行体外评价,包括重量变化、硬度、漂浮时间、药物含量和药物释放。结果表明,制备的载药长丝成功打印出胃漂浮制剂。盐酸维拉帕米在热熔挤出和熔融沉积建模过程中热稳定,在长丝和打印制剂中呈无定形状态。打印制剂的形状和填充率影响硬度、漂浮时间和体外药物释放。