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Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate

Polycaprolactone (PCL) is drawing increasing attention in the field of medical 3D printing and tissue engineering because of its biodegradability. This study developed polycaprolactone prepolymers that can be cured using visible light. Three PCL acrylates were synthesized: polycaprolactone-530 diacr...

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Autores principales: Tzeng, Jy-Jiunn, Hsiao, Yi-Ting, Wu, Yun-Ching, Chen, Hsuan, Lee, Shyh-Yuan, Lin, Yuan-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964557/
https://www.ncbi.nlm.nih.gov/pubmed/29854803
http://dx.doi.org/10.1155/2018/8719624
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author Tzeng, Jy-Jiunn
Hsiao, Yi-Ting
Wu, Yun-Ching
Chen, Hsuan
Lee, Shyh-Yuan
Lin, Yuan-Min
author_facet Tzeng, Jy-Jiunn
Hsiao, Yi-Ting
Wu, Yun-Ching
Chen, Hsuan
Lee, Shyh-Yuan
Lin, Yuan-Min
author_sort Tzeng, Jy-Jiunn
collection PubMed
description Polycaprolactone (PCL) is drawing increasing attention in the field of medical 3D printing and tissue engineering because of its biodegradability. This study developed polycaprolactone prepolymers that can be cured using visible light. Three PCL acrylates were synthesized: polycaprolactone-530 diacrylate (PCL530DA), glycerol-3 caprolactone triacrylate (Glycerol-3CL-TA), and glycerol-6 caprolactone triacrylate (Glycerol-6CL-TA). PCL530DA has two acrylates, whereas Glycerol-3CL-TA and Glycerol-6CL-TA have three acrylates. The Fourier transform infrared and nuclear magnetic resonance spectra suggested successful synthesis of all PCL acrylates. All are liquid at room temperature and can be photopolymerized into a transparent solid after exposure to 470 nm blue LED light using 1% camphorquinone as photoinitiator and 2% dimethylaminoethyl methacrylate as coinitiator. The degree of conversion for all PCL acrylates can reach more than 80% after 1 min of curing. The compressive modulus of PCL530DA, Glycerol-3CL-TA, and Glycerol-6CL-TA is 65.7 ± 12.7, 80.9 ± 6.1, and 32.1 ± 4.1 MPa, respectively, and their compressive strength is 5.3 ± 0.29, 8.3 ± 0.18, and 3.0 ± 0.53 MPa, respectively. Thus, all PCL acrylates synthesized in this study can be photopolymerized and because of their solid structure and low viscosity, they are applicable to soft tissue engineering and medical 3D printing.
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spelling pubmed-59645572018-05-31 Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate Tzeng, Jy-Jiunn Hsiao, Yi-Ting Wu, Yun-Ching Chen, Hsuan Lee, Shyh-Yuan Lin, Yuan-Min Biomed Res Int Research Article Polycaprolactone (PCL) is drawing increasing attention in the field of medical 3D printing and tissue engineering because of its biodegradability. This study developed polycaprolactone prepolymers that can be cured using visible light. Three PCL acrylates were synthesized: polycaprolactone-530 diacrylate (PCL530DA), glycerol-3 caprolactone triacrylate (Glycerol-3CL-TA), and glycerol-6 caprolactone triacrylate (Glycerol-6CL-TA). PCL530DA has two acrylates, whereas Glycerol-3CL-TA and Glycerol-6CL-TA have three acrylates. The Fourier transform infrared and nuclear magnetic resonance spectra suggested successful synthesis of all PCL acrylates. All are liquid at room temperature and can be photopolymerized into a transparent solid after exposure to 470 nm blue LED light using 1% camphorquinone as photoinitiator and 2% dimethylaminoethyl methacrylate as coinitiator. The degree of conversion for all PCL acrylates can reach more than 80% after 1 min of curing. The compressive modulus of PCL530DA, Glycerol-3CL-TA, and Glycerol-6CL-TA is 65.7 ± 12.7, 80.9 ± 6.1, and 32.1 ± 4.1 MPa, respectively, and their compressive strength is 5.3 ± 0.29, 8.3 ± 0.18, and 3.0 ± 0.53 MPa, respectively. Thus, all PCL acrylates synthesized in this study can be photopolymerized and because of their solid structure and low viscosity, they are applicable to soft tissue engineering and medical 3D printing. Hindawi 2018-05-08 /pmc/articles/PMC5964557/ /pubmed/29854803 http://dx.doi.org/10.1155/2018/8719624 Text en Copyright © 2018 Jy-Jiunn Tzeng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tzeng, Jy-Jiunn
Hsiao, Yi-Ting
Wu, Yun-Ching
Chen, Hsuan
Lee, Shyh-Yuan
Lin, Yuan-Min
Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title_full Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title_fullStr Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title_full_unstemmed Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title_short Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate
title_sort synthesis, characterization, and visible light curing capacity of polycaprolactone acrylate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964557/
https://www.ncbi.nlm.nih.gov/pubmed/29854803
http://dx.doi.org/10.1155/2018/8719624
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