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HERO ID
7916624
Reference Type
Journal Article
Title
Investigating Photocurable Thiol-Yne Resins for Biomedical Materials
Author(s)
Oesterreicher, A; Moser, A; Edler, M; Griesser, H; Schloegl, S; Pichelmayer, M; Griesser, T
Year
2017
Is Peer Reviewed?
1
Journal
Macromolecular Materials & Engineering
ISSN:
1438-7492
Publisher
Wiley-VCH Verlag
Volume
302
Issue
5
Language
English
DOI
10.1002/mame.201600450
Web of Science Id
WOS:000401186200001
Abstract
This study deals with the investigation of photocurable thiol-yne resins covering several important aspects for the production of medical devices by UV-based manufacturing processes. In this context, the performance of different low-toxic photoinitiators (PIs) and stabilizers are evaluated in thiol-yne formulations based on di(but-1-yn-4-yl) carbonate and various multifunctional thiol monomers. Photodifferential scanning calorimetry measurements reveal that the conversion of all resin formulations is mostly independent on the type and concentration of the applied photoinitiator; however, significant differences in their curing speed are observed. It turns out that the migration of an alkyne derivatized photoinitiator is significantly reduced while providing almost similar photoactivity as its nonfunctionalized reference. Moreover, it is found that lauryl gallate and butylated hydroxytoluene lead to significant stabilization without affecting the overall photoreactivity. Notably, the thermomechanical properties of the investigated photopolymers are only slightly affected by water absorption. Using ester free thiols, water absorption can be reduced and hydrolytically stable polymers are realized. These results highlight the versatility of the present thiol-yne system for the production of medical materials by photopolymerization. (Figure presented.). © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
biomedical materials; photopolymerization; thiol-yne
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