Three-Dimensional Printing of Drug-Eluting Implants: Preparation of an Antimicrobial Polylactide Feedstock Material

被引:114
|
作者
Water, Jorrit Jeroen [1 ]
Bohr, Adam [2 ]
Boetker, Johan [2 ]
Aho, Johanna [2 ]
Sandler, Niklas [3 ]
Nielsen, Hanne Morck [1 ]
Rantanen, Jukka [2 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, Sect Biol, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, Sect Pharmaceut Technol & Engn, DK-2100 Copenhagen, Denmark
[3] Abo Akad Univ, Dept Biosci, Pharmaceut Sci Lab, FI-20520 Turku, Finland
关键词
biomaterials; extrusion; polymeric drug delivery systems; poly(lactic; glycolic) acid (PLGA or PLA); controlled release; anti-infectives; spectroscopy; polymers; microscopy; drug delivery systems; BIOFILM FORMATION; HYDROXYAPATITE; DEVICES; BIOMATERIALS; FABRICATION; SCAFFOLDS; INFECTION; MATRICES; TABLETS; DESIGN;
D O I
10.1002/jps.24305
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of the present work was to investigate the potential of three-dimensional (3D) printing as a manufacturing method for products intended for personalized treatments by exploring the production of novel polylactide-based feedstock materials for 3D printing purposes. Nitrofurantoin (NF) and hydroxyapatite (HA) were successfully mixed and extruded with up to 30% drug load with and without addition of 5% HA in polylactide strands, which were subsequently 3D-printed into model disc geometries (10 x 2 mm). X-ray powder diffraction analysis showed that NF maintained its anhydrate solid form during the processing. Release of NF from the disks was dependent on the drug loading in a concentration-dependent manner as a higher level of released drug was observed from disks with higher drug loads. Disks with 30% drug loading were able to prevent surface-associated and planktonic growth of Staphylococcus aureus over a period of 7 days. At 10% drug loading, the disks did not inhibit planktonic growth, but still inhibited surface-associated growth. Elemental analysis indicated the presence of microdomains of solid drug supporting the observed slow and partial drug release. This work demonstrates the potential of custom-made, drug-loaded feedstock materials for 3D printing of pharmaceutical products for controlled release. (c) 2015 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:1099-1107, 2015
引用
收藏
页码:1099 / 1107
页数:9
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