Goyanes Alvaro, Fina Fabrizio, Martorana Annalisa, Sedough Daniel, Gaisford Simon, Basit Abdul W
FabRx Ltd., 3 Romney Road, Ashford, Kent, TN24 0RW, UK.
UCL School of Pharmacy, University College London,29-39 Brunswick Square, London, WC1N 1AX, UK.
Int J Pharm. 2017 Jul 15;527(1-2):21-30. doi: 10.1016/j.ijpharm.2017.05.021. Epub 2017 May 11.
The aim of this study was to manufacture 3D printed tablets (printlets) from enteric polymers by single filament fused deposition modeling (FDM) 3D printing (3DP). Hot melt extrusion was used to generate paracetamol-loaded filaments from three different grades of the pharmaceutical excipient hypromellose acetate succinate (HPMCAS), grades LG, MG and HG. One-step 3DP was used to process these filaments into enteric printlets incorporating up to 50% drug loading with two different infill percentages (20 and 100%). X-ray Micro Computed Tomography (Micro-CT) analysis revealed that printlets with 20% infill had cavities in the core compared to 100% infill, and that the density of the 50% drug loading printlets was higher than the equivalent formulations loaded with 5% drug. In biorelevant bicarbonate dissolution media, drug release from the printlets was dependent on the polymer composition, drug loading and the internal structure of the formulations. All HPMCAS-based printlets showed delayed drug release properties, and in the intestinal conditions, drug release was faster from the printlets prepared with polymers with a lower pH-threshold: HPMCAS LG > HPMCAS MG > HPMCAS HG. These results confirm that FDM 3D printing makes it possible not only to manufacture delayed release printlets without the need for an outer enteric coating, but it is also feasible to adapt the release profile in response to the personal characteristics of the patient, realizing the full potential of additive manufacturing in the development of personalised dose medicines.
本研究的目的是通过单丝熔融沉积建模(FDM)3D打印(3DP)技术,使用肠溶聚合物制造3D打印片剂(打印片)。采用热熔挤出法,以三种不同等级的药用辅料醋酸羟丙甲纤维素琥珀酸酯(HPMCAS)(LG、MG和HG等级)制备了载有扑热息痛的长丝。采用一步3D打印法将这些长丝加工成肠溶打印片,药物载量高达50%,填充率分别为20%和100%。X射线微计算机断层扫描(Micro-CT)分析显示,填充率为20%的打印片与填充率为100%的打印片相比,其核心有孔洞,且载药量为50%的打印片密度高于载药量为5%的等效制剂。在生物相关的碳酸氢盐溶解介质中,打印片中药物的释放取决于聚合物组成、药物载量和制剂的内部结构。所有基于HPMCAS的打印片均显示出延迟释药特性,且在肠道条件下,由pH阈值较低的聚合物制备的打印片中药物释放更快:HPMCAS LG > HPMCAS MG > HPMCAS HG。这些结果证实,FDM 3D打印不仅能够制造无需外部肠溶包衣的延迟释放打印片,而且根据患者的个人特征调整释放曲线也是可行的,这实现了增材制造在个性化给药开发中的全部潜力。