Roadmap to 3D-Printed Oral Pharmaceutical Dosage Forms: Feedstock Filament Properties and Characterization for Fused Deposition Modeling

被引:106
作者
Aho, Johanna [1 ]
Botker, Johan Peter [1 ]
Genina, Natalja [1 ]
Edinger, Magnus [1 ]
Arnfast, Laerke [1 ]
Rantanen, Jukka [1 ]
机构
[1] Univ Copenhagen, Dept Pharm, Univ Pk 2, DK-2100 Copenhagen, Denmark
关键词
rheology; extrusion; polymer(s); printing (3D); simulation(s); thermal analysis; mechanical properties; HOT-MELT EXTRUSION; POLY-EPSILON-CAPROLACTONE; SOLID DISPERSIONS; DRUG-RELEASE; EXTRUDATE SWELL; 3D; FDM; BEHAVIOR; TABLETS; FRACTURE;
D O I
10.1016/j.xphs.2018.11.012
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Application of additive manufacturing techniques (3D printing) for mass-customized products has boomed in the recent years. In pharmaceutical industry and research, the interest has grown particularly with the future scenario of more personalized medicinal products. Understanding a broad range of material properties and process behavior of the drug-excipient combinations is necessary for successful 3D printing of dosage forms. This commentary reviews recent 3D-printing studies by fused deposition modeling (FDM) technique in pharmaceutical sciences, extending into the fields of polymer processing and rapid prototyping, where more in-depth studies on the feedstock material properties, modeling, and simulation of the FDM process have been performed. A case study of a model oral dosage form from custom-prepared indomethacin-polycaprolactone feedstock filament was used as an example in the pharmaceutical context. The printability was assessed in the different process steps: preparation of customized filaments for FDM, filament feeding, deposition, and solidification. These were linked with the rheological, thermal, and mechanical properties and their characterization, relevant for understanding the printability of drug products by FDM. (c) 2019 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:26 / 35
页数:10
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