| Literature DB >> 25640314 |
Jorrit Jeroen Water1, Adam Bohr, Johan Boetker, Johanna Aho, Niklas Sandler, Hanne Mørck Nielsen, Jukka Rantanen.
Abstract
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 × 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.Entities:
Keywords: anti-infectives; biomaterials; controlled release; drug delivery systems; extrusion; microscopy; poly(lactic/glycolic) acid (PLGA or PLA); polymeric drug delivery systems; polymers; spectroscopy
Mesh:
Substances:
Year: 2015 PMID: 25640314 DOI: 10.1002/jps.24305
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534