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Development of a fast curing tissue adhesive for meniscus tear repair
Isocyanate-terminated adhesive amphiphilic block copolymers are attractive materials to treat meniscus tears due to their tuneable mechanical properties and good adhesive characteristics. However, a drawback of this class of materials is their relatively long curing time. In this study, we evaluate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116306/ https://www.ncbi.nlm.nih.gov/pubmed/27866344 http://dx.doi.org/10.1007/s10856-016-5790-6 |
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author | Bochyńska, Agnieszka Izabela Hannink, Gerjon Janssen, Dennis Buma, Pieter Grijpma, Dirk W. |
author_facet | Bochyńska, Agnieszka Izabela Hannink, Gerjon Janssen, Dennis Buma, Pieter Grijpma, Dirk W. |
author_sort | Bochyńska, Agnieszka Izabela |
collection | PubMed |
description | Isocyanate-terminated adhesive amphiphilic block copolymers are attractive materials to treat meniscus tears due to their tuneable mechanical properties and good adhesive characteristics. However, a drawback of this class of materials is their relatively long curing time. In this study, we evaluate the use of an amine cross-linker and addition of catalysts as two strategies to accelerate the curing rates of a recently developed biodegradable reactive isocyanate-terminated hyper-branched adhesive block copolymer prepared from polyethylene glycol (PEG), trimethylene carbonate, citric acid and hexamethylene diisocyanate. The curing kinetics of the hyper-branched adhesive alone and in combination with different concentrations of spermidine solutions, and after addition of 2,2-dimorpholinodiethylether (DMDEE) or 1,4-diazabicyclo [2.2.2] octane (DABCO) were determined using FTIR. Additionally, lap-shear adhesion tests using all compositions at various time points were performed. The two most promising compositions of the fast curing adhesives were evaluated in a meniscus bucket handle lesion model and their performance was compared with that of fibrin glue. The results showed that addition of both spermidine and catalysts to the adhesive copolymer can accelerate the curing rate and that firm adhesion can already be achieved after 2 h. The adhesive strength to meniscus tissue of 3.2–3.7 N was considerably higher for the newly developed compositions than for fibrin glue (0.3 N). The proposed combination of an adhesive component and a cross-linking component or catalyst is a promising way to accelerate curing rates of isocyanate-terminated tissue adhesives. |
format | Online Article Text |
id | pubmed-5116306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-51163062016-12-02 Development of a fast curing tissue adhesive for meniscus tear repair Bochyńska, Agnieszka Izabela Hannink, Gerjon Janssen, Dennis Buma, Pieter Grijpma, Dirk W. J Mater Sci Mater Med Biomaterials Synthesis and Characterization Isocyanate-terminated adhesive amphiphilic block copolymers are attractive materials to treat meniscus tears due to their tuneable mechanical properties and good adhesive characteristics. However, a drawback of this class of materials is their relatively long curing time. In this study, we evaluate the use of an amine cross-linker and addition of catalysts as two strategies to accelerate the curing rates of a recently developed biodegradable reactive isocyanate-terminated hyper-branched adhesive block copolymer prepared from polyethylene glycol (PEG), trimethylene carbonate, citric acid and hexamethylene diisocyanate. The curing kinetics of the hyper-branched adhesive alone and in combination with different concentrations of spermidine solutions, and after addition of 2,2-dimorpholinodiethylether (DMDEE) or 1,4-diazabicyclo [2.2.2] octane (DABCO) were determined using FTIR. Additionally, lap-shear adhesion tests using all compositions at various time points were performed. The two most promising compositions of the fast curing adhesives were evaluated in a meniscus bucket handle lesion model and their performance was compared with that of fibrin glue. The results showed that addition of both spermidine and catalysts to the adhesive copolymer can accelerate the curing rate and that firm adhesion can already be achieved after 2 h. The adhesive strength to meniscus tissue of 3.2–3.7 N was considerably higher for the newly developed compositions than for fibrin glue (0.3 N). The proposed combination of an adhesive component and a cross-linking component or catalyst is a promising way to accelerate curing rates of isocyanate-terminated tissue adhesives. Springer US 2016-11-19 2017 /pmc/articles/PMC5116306/ /pubmed/27866344 http://dx.doi.org/10.1007/s10856-016-5790-6 Text en © The Author(s) 2016 This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Biomaterials Synthesis and Characterization Bochyńska, Agnieszka Izabela Hannink, Gerjon Janssen, Dennis Buma, Pieter Grijpma, Dirk W. Development of a fast curing tissue adhesive for meniscus tear repair |
title | Development of a fast curing tissue adhesive for meniscus tear repair |
title_full | Development of a fast curing tissue adhesive for meniscus tear repair |
title_fullStr | Development of a fast curing tissue adhesive for meniscus tear repair |
title_full_unstemmed | Development of a fast curing tissue adhesive for meniscus tear repair |
title_short | Development of a fast curing tissue adhesive for meniscus tear repair |
title_sort | development of a fast curing tissue adhesive for meniscus tear repair |
topic | Biomaterials Synthesis and Characterization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116306/ https://www.ncbi.nlm.nih.gov/pubmed/27866344 http://dx.doi.org/10.1007/s10856-016-5790-6 |
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