Azad Mohammad A, Olawuni Deborah, Kimbell Georgia, Badruddoza Abu Zayed Md, Hossain Md Shahadat, Sultana Tasnim
Department of Chemical, Biological and Bioengineering, North Carolina A&T State University, Greensboro, NC 27411, USA.
Department of Chemical and Life Sciences Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA.
Pharmaceutics. 2020 Feb 3;12(2):124. doi: 10.3390/pharmaceutics12020124.
Three dimensional (3D) printing as an advanced manufacturing technology is progressing to be established in the pharmaceutical industry to overcome the traditional manufacturing regime of 'one size fits for all'. Using 3D printing, it is possible to design and develop complex dosage forms that can be suitable for tuning drug release. Polymers are the key materials that are necessary for 3D printing. Among all 3D printing processes, extrusion-based (both fused deposition modeling (FDM) and pressure-assisted microsyringe (PAM)) 3D printing is well researched for pharmaceutical manufacturing. It is important to understand which polymers are suitable for extrusion-based 3D printing of pharmaceuticals and how their properties, as well as the behavior of polymer-active pharmaceutical ingredient (API) combinations, impact the printing process. Especially, understanding the rheology of the polymer and API-polymer mixtures is necessary for successful 3D printing of dosage forms or printed structures. This review has summarized a holistic materials-process perspective for polymers on extrusion-based 3D printing. The main focus herein will be both FDM and PAM 3D printing processes. It elaborates the discussion on the comparison of 3D printing with the traditional direct compression process, the necessity of rheology, and the characterization techniques required for the printed structure, drug, and excipients. The current technological challenges, regulatory aspects, and the direction toward which the technology is moving, especially for personalized pharmaceuticals and multi-drug printing, are also briefly discussed.
三维(3D)打印作为一种先进的制造技术,正在制药行业中逐步确立,以克服传统的“一刀切”制造模式。使用3D打印,可以设计和开发适合调节药物释放的复杂剂型。聚合物是3D打印所需的关键材料。在所有3D打印工艺中,基于挤出的3D打印(包括熔融沉积建模(FDM)和压力辅助微注射器(PAM))在药物制造方面得到了充分研究。了解哪些聚合物适用于基于挤出的药物3D打印,以及它们的性能以及聚合物-活性药物成分(API)组合的行为如何影响打印过程非常重要。特别是,了解聚合物和API-聚合物混合物的流变学对于成功进行剂型或打印结构的3D打印是必要的。本综述从整体材料-工艺角度总结了聚合物在基于挤出的3D打印方面的情况。本文的主要重点将是FDM和PAM 3D打印工艺。它详细讨论了3D打印与传统直接压缩工艺的比较、流变学的必要性以及打印结构、药物和辅料所需的表征技术。还简要讨论了当前的技术挑战、监管方面以及该技术的发展方向,特别是针对个性化药物和多药物打印。