A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use

It has been a great challenge to develop aldehyde-free tissue adhesives that can function rapidly and controllably on wet internal tissues with fine adhesion strength, sound biocompatibility and degradability. To this end, we have devised a mussel-inspired easy-to-use double-crosslink tissue adhesiv...

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Main Authors: Fan, Changjiang, Fu, Jiayin, Zhu, Wenzhen, Wang, Dong-An
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/84685
http://hdl.handle.net/10220/41957
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-846852020-03-07T11:35:28Z A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use Fan, Changjiang Fu, Jiayin Zhu, Wenzhen Wang, Dong-An School of Chemical and Biomedical Engineering Tissue adhesive Dopamine It has been a great challenge to develop aldehyde-free tissue adhesives that can function rapidly and controllably on wet internal tissues with fine adhesion strength, sound biocompatibility and degradability. To this end, we have devised a mussel-inspired easy-to-use double-crosslink tissue adhesive (DCTA) comprising a dopamine-conjugated gelatin macromer, a rapid crosslinker (namely, Fe3+), and a long-term acting crosslinker (namely, genipin). As a mussel-inspired gluing macromer, dopamine is grafted onto gelatin backbone via an one-step reaction, the catechol groups of which are capable of performing strong wet adhesion on tissue surfaces. By addition of genipin and Fe3+, the formation of catechol–Fe3+ complexation and accompanying spontaneous curing of genipin-primed covalent crosslinking of gluing macromers in one pot endows DCTA with the double-crosslink adhesion mechanism. Namely, the reversible catechol–Fe3+ crosslinking executes an controllable and instant adhesive curing; while genipin-induced stable covalent crosslinking promises it with long-term effectiveness. This novel DCTA exhibits significantly higher wet tissue adhesion capability than the commercially available fibrin glue when applied on wet porcine skin and cartilage. In addition, this DCTA also demonstrates fine elasticity, sound biodegradability, and biocompatibility when contacting in vitro cultured cells and blood. In vivo biocompatibility and biodegradability are checked and confirmed via trials of subcutaneous implantation in nude mice model. This newly developed DCTA may be a highly promising product as a biological glue for internal medical use including internal tissue adhesion, sealing, and hemostasis. MOE (Min. of Education, S’pore) 2016-12-28T09:12:44Z 2019-12-06T15:49:29Z 2016-12-28T09:12:44Z 2019-12-06T15:49:29Z 2016 Journal Article Fan, C., Fu, J., Zhu, W., & Wang, D.-A. (2016). A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use. Acta Biomaterialia, 33, 51-63. 1742-7061 https://hdl.handle.net/10356/84685 http://hdl.handle.net/10220/41957 10.1016/j.actbio.2016.02.003 en Acta Biomaterialia © 2016 Acta Materialia Inc. (published by Elsevier). 13 p.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Tissue adhesive
Dopamine
spellingShingle Tissue adhesive
Dopamine
Fan, Changjiang
Fu, Jiayin
Zhu, Wenzhen
Wang, Dong-An
A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
description It has been a great challenge to develop aldehyde-free tissue adhesives that can function rapidly and controllably on wet internal tissues with fine adhesion strength, sound biocompatibility and degradability. To this end, we have devised a mussel-inspired easy-to-use double-crosslink tissue adhesive (DCTA) comprising a dopamine-conjugated gelatin macromer, a rapid crosslinker (namely, Fe3+), and a long-term acting crosslinker (namely, genipin). As a mussel-inspired gluing macromer, dopamine is grafted onto gelatin backbone via an one-step reaction, the catechol groups of which are capable of performing strong wet adhesion on tissue surfaces. By addition of genipin and Fe3+, the formation of catechol–Fe3+ complexation and accompanying spontaneous curing of genipin-primed covalent crosslinking of gluing macromers in one pot endows DCTA with the double-crosslink adhesion mechanism. Namely, the reversible catechol–Fe3+ crosslinking executes an controllable and instant adhesive curing; while genipin-induced stable covalent crosslinking promises it with long-term effectiveness. This novel DCTA exhibits significantly higher wet tissue adhesion capability than the commercially available fibrin glue when applied on wet porcine skin and cartilage. In addition, this DCTA also demonstrates fine elasticity, sound biodegradability, and biocompatibility when contacting in vitro cultured cells and blood. In vivo biocompatibility and biodegradability are checked and confirmed via trials of subcutaneous implantation in nude mice model. This newly developed DCTA may be a highly promising product as a biological glue for internal medical use including internal tissue adhesion, sealing, and hemostasis.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Fan, Changjiang
Fu, Jiayin
Zhu, Wenzhen
Wang, Dong-An
format Article
author Fan, Changjiang
Fu, Jiayin
Zhu, Wenzhen
Wang, Dong-An
author_sort Fan, Changjiang
title A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
title_short A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
title_full A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
title_fullStr A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
title_full_unstemmed A mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
title_sort mussel-inspired double-crosslinked tissue adhesive intended for internal medical use
publishDate 2016
url https://hdl.handle.net/10356/84685
http://hdl.handle.net/10220/41957
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