Abstract
To establish photopolymers for the production of class II or class III medical products by additive manufacturing it is essential to know which components of photopolymeric systems, consisting of monomers, photoinitiators and additives, are the determining factors on their biocompatible properties. In this study the leachable substances of a cured photopolymeric system were eluted and identified by HPLC-MS detection. In addition the cured photopolymer was testes for cytotoxicity and genotoxicity according to DIN EN ISO 10993 for long time applications. The results showed that uncured residual monomers are the determining factor on the biocompatible properties of the photopolymeric system. Strategies to reduce these residual monomers in the cured photopolymer are presented.
Original language | English |
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Pages (from-to) | 113-116 |
Number of pages | 4 |
Journal | Current Directions in Biomedical Engineering |
Volume | 2 |
Issue number | 1 |
DOIs | |
State | Published - Sep 2016 |
Keywords
- Additive manufacturing
- Biocompatibility
- Digital light processing
- Monomers
- Patient individual medical products
- Photopolymeric system