共 31 条
Three-Dimensional Printing of Drug-Eluting Implants: Preparation of an Antimicrobial Polylactide Feedstock Material
被引:118
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
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页码:1099 / 1107
页数:9
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