| Literature DB >> 34044092 |
Ioannis Koutsamanis1, Amrit Paudel2, Carolina Patricia Alva Zúñiga1, Laura Wiltschko1, Martin Spoerk3.
Abstract
To improve patient compliance and personalised drug delivery, long-acting drug delivery devices (LADDDs), such as implants and inserts, greatly benefit from a customisation in their shape through the emerging 3D-printing technology, since their production usually follows a one-size-fits-most approach. The use of 3D-printing for LADDDs, however, is mainly limited by the shortage of flawlessly 3D-printable, yet biocompatible materials. The present study tackles this issue by introducing a novel, non-biodegradable material, namely a polyester-based thermoplastic elastomer (TPC) - a multi-block copolymer containing alternating semi-crystalline polybutylene terephthalate hard segments and poly-ether-terephthalate amorphous soft segments. Next to a detailed description of the material's 3D-printability by mechanical, rheological and thermal analyses, which was found to be superior to that of conventional polymers (ethylene-vinyl acetates (EVA)), this study establishes the fundamental understandings of the interactions between progesterone (P4) and TPC and drug-releasing properties of TPC for the first time. P4-loaded LADDDs based on TPC, prepared via an elaborated solvent-immersion technique, enable the release of P4 at pharmacologically relevant rates, similar to those of marketed formulations based on EVA and silicones. Additionally, TPC demonstrated an exceptional 3D-printability for a wide selection of implant sizes and complex geometries.Entities:
Keywords: 3D-printing; Hot-melt extrusion; Implant; Non-biodegradable polymer; Progesterone; Urethra pessary; Vaginal drug delivery
Year: 2021 PMID: 34044092 DOI: 10.1016/j.jconrel.2021.05.030
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776