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熔融沉积成型增材制造的研究 I:工艺温度对剂型质量和结晶度的影响。

Investigation of the Fused Deposition Modeling Additive Manufacturing I: Influence of Process Temperature on the Quality and Crystallinity of the Dosage Forms.

机构信息

Pharmaceutical Engineering and 3D Printing (PharmE3D) Lab, Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX, 78712, USA.

出版信息

AAPS PharmSciTech. 2021 Oct 25;22(8):258. doi: 10.1208/s12249-021-02094-8.

DOI:10.1208/s12249-021-02094-8
PMID:34697652
Abstract

With the advancements in cutting-edge technologies and rapid development of medical sciences, patient-focused drug development (PFDD) through additive manufacturing (AM) processes is gathering more interest in the pharmaceutical area than ever. Hence, there is an urgent need for researchers to comprehensively understand the influence of three-dimensional design on the development of novel drug delivery systems (DDSs). For this research, fused deposition modeling (FDM) 3D printing was investigated, and phenytoin (PHT) was selected as the model drug. The primary purpose of the current investigation was to understand the influence of AM process on the pharmaceutical products' quality. A series of comparative studies, including morphology, solid-state analysis, and in vitro drug release studies between additive manufactured filaments (printlets) and extruded filaments, were conducted. The FDM-based AM showed adequate reproducibility by manufacturing printlets with consistent qualities; however, the model slicing orientation significantly affected the print qualities. The texture analysis studies showed that the mechanical properties (breaking behavior) of additive manufactured printlets were varied from the extruded filaments. Additionally, the higher printing temperature also influenced the solid state of the drug where the process assisted in PHT's amorphization in the printed products, which further affected their mechanical properties and in vitro drug release performances. The current investigation illustrated that the AM process would change the printed objects' macrostructure over the conventional products, and the printing temperature and slicing will significantly affect the printing process and product qualities.

摘要

随着尖端技术的进步和医学科学的快速发展,通过增材制造(AM)工艺以患者为中心的药物开发(PFDD)在制药领域比以往任何时候都更受关注。因此,研究人员迫切需要全面了解三维设计对新型药物输送系统(DDS)开发的影响。为此,研究了熔融沉积建模(FDM)3D 打印,并选择苯妥英(PHT)作为模型药物。本研究的主要目的是了解 AM 工艺对药物产品质量的影响。进行了一系列对比研究,包括形态学、固态分析和体外药物释放研究,比较了增材制造丝(printlets)和挤出丝之间的差异。基于 FDM 的 AM 通过制造具有一致质量的 printlets 显示出足够的可重复性;然而,模型切片方向显著影响打印质量。纹理分析研究表明,增材制造的 printlets 的机械性能(断裂行为)与挤出丝不同。此外,较高的打印温度也会影响药物的固态,其中该工艺有助于在打印产品中使 PHT 非晶化,这进一步影响了它们的机械性能和体外药物释放性能。本研究表明,AM 工艺会改变打印物体相对于传统产品的宏观结构,而打印温度和切片会显著影响打印过程和产品质量。

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