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A biocompatible macromolecular two-photon initiator based on hyaluronan
The possibility of the direct encapsulation of living cells via two-photon induced photopolymerization enables the microfabrication of hydrogel scaffolds with high initial cell loadings and intimate matrix–cell contact. While highly efficient water-soluble two-photon initiators based on benzylidene...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310395/ https://www.ncbi.nlm.nih.gov/pubmed/28261331 http://dx.doi.org/10.1039/c6py01787h |
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author | Tromayer, Maximilian Gruber, Peter Markovic, Marica Rosspeintner, Arnulf Vauthey, Eric Redl, Heinz Ovsianikov, Aleksandr Liska, Robert |
author_facet | Tromayer, Maximilian Gruber, Peter Markovic, Marica Rosspeintner, Arnulf Vauthey, Eric Redl, Heinz Ovsianikov, Aleksandr Liska, Robert |
author_sort | Tromayer, Maximilian |
collection | PubMed |
description | The possibility of the direct encapsulation of living cells via two-photon induced photopolymerization enables the microfabrication of hydrogel scaffolds with high initial cell loadings and intimate matrix–cell contact. While highly efficient water-soluble two-photon initiators based on benzylidene ketone dyes have been developed, they exhibit considerable cyto- and phototoxicity. To address the problem of photoinitiator migration from the extracellular matrix into the cytosol, a two-photon initiator bound to a polymeric hyaluronan backbone (HAPI) was synthesized in this work. HAPI exhibited a distinct improvement of cytocompatibility compared to a reference two-photon initiator. Basic photophysical investigations were performed to characterize the absorption and fluorescence behavior of HAPI. Laser scanning microscopy was used to visualize and confirm the hindered transmembrane migration behavior of HAPI. The performance of HAPI was tested in two-photon polymerization at exceedingly high printing speeds of 100 mm s(–1) producing gelatin-based complex 3D hydrogel scaffolds with a water content of 85%. The photodamage of the structuring process was low and viable MC3T3 cells embedded in the gel were monitored for several days after structuring. |
format | Online Article Text |
id | pubmed-5310395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-53103952017-03-01 A biocompatible macromolecular two-photon initiator based on hyaluronan Tromayer, Maximilian Gruber, Peter Markovic, Marica Rosspeintner, Arnulf Vauthey, Eric Redl, Heinz Ovsianikov, Aleksandr Liska, Robert Polym Chem Chemistry The possibility of the direct encapsulation of living cells via two-photon induced photopolymerization enables the microfabrication of hydrogel scaffolds with high initial cell loadings and intimate matrix–cell contact. While highly efficient water-soluble two-photon initiators based on benzylidene ketone dyes have been developed, they exhibit considerable cyto- and phototoxicity. To address the problem of photoinitiator migration from the extracellular matrix into the cytosol, a two-photon initiator bound to a polymeric hyaluronan backbone (HAPI) was synthesized in this work. HAPI exhibited a distinct improvement of cytocompatibility compared to a reference two-photon initiator. Basic photophysical investigations were performed to characterize the absorption and fluorescence behavior of HAPI. Laser scanning microscopy was used to visualize and confirm the hindered transmembrane migration behavior of HAPI. The performance of HAPI was tested in two-photon polymerization at exceedingly high printing speeds of 100 mm s(–1) producing gelatin-based complex 3D hydrogel scaffolds with a water content of 85%. The photodamage of the structuring process was low and viable MC3T3 cells embedded in the gel were monitored for several days after structuring. Royal Society of Chemistry 2017-01-14 2016-11-29 /pmc/articles/PMC5310395/ /pubmed/28261331 http://dx.doi.org/10.1039/c6py01787h Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Tromayer, Maximilian Gruber, Peter Markovic, Marica Rosspeintner, Arnulf Vauthey, Eric Redl, Heinz Ovsianikov, Aleksandr Liska, Robert A biocompatible macromolecular two-photon initiator based on hyaluronan |
title | A biocompatible macromolecular two-photon initiator based on hyaluronan
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title_full | A biocompatible macromolecular two-photon initiator based on hyaluronan
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title_fullStr | A biocompatible macromolecular two-photon initiator based on hyaluronan
|
title_full_unstemmed | A biocompatible macromolecular two-photon initiator based on hyaluronan
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title_short | A biocompatible macromolecular two-photon initiator based on hyaluronan
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title_sort | biocompatible macromolecular two-photon initiator based on hyaluronan |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310395/ https://www.ncbi.nlm.nih.gov/pubmed/28261331 http://dx.doi.org/10.1039/c6py01787h |
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