Cargando…

Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive

Hydrolysis resistance is essential to the durability of the dentin bonding interface. Urushiol is a natural monomer that has been used in different fields over thousands of years but has the disadvantage of a long drying time. In this study, we evaluated a novel photocurable derivative of urushiol a...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ying, He, Xi, Wang, Han, Zhu, Jiufu, Wang, Huimin, Zheng, Yan, Zhu, Song, Cui, Zhanchen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033433/
https://www.ncbi.nlm.nih.gov/pubmed/35480923
http://dx.doi.org/10.1039/d1ra00471a
_version_ 1784692887459463168
author Zhao, Ying
He, Xi
Wang, Han
Zhu, Jiufu
Wang, Huimin
Zheng, Yan
Zhu, Song
Cui, Zhanchen
author_facet Zhao, Ying
He, Xi
Wang, Han
Zhu, Jiufu
Wang, Huimin
Zheng, Yan
Zhu, Song
Cui, Zhanchen
author_sort Zhao, Ying
collection PubMed
description Hydrolysis resistance is essential to the durability of the dentin bonding interface. Urushiol is a natural monomer that has been used in different fields over thousands of years but has the disadvantage of a long drying time. In this study, we evaluated a novel photocurable derivative of urushiol as the main monomer for polymerization in dentin adhesive and its effect on hydrolysis resistance. The derivative was characterized by Fourier transform infrared spectroscopy and (1)H nuclear magnetic resonance spectroscopy. Compared with the Adper Single Bond 2, the experimentally synthesized adhesives had higher contact angles. In particular, the water sorption/solubility of the experimental samples were significantly lower than that of Adper Single Bond 2. The microtensile bond strengths of the test groups were higher than that of the control group, even after 5000 thermocycles. Cytotoxicity test results showed that adhesives based on the original derivative induced low toxicity to L929 cells. The results of this study may shift the focus of future research to natural monomers and even their derivatives which may perform well in dentistry.
format Online
Article
Text
id pubmed-9033433
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90334332022-04-26 Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive Zhao, Ying He, Xi Wang, Han Zhu, Jiufu Wang, Huimin Zheng, Yan Zhu, Song Cui, Zhanchen RSC Adv Chemistry Hydrolysis resistance is essential to the durability of the dentin bonding interface. Urushiol is a natural monomer that has been used in different fields over thousands of years but has the disadvantage of a long drying time. In this study, we evaluated a novel photocurable derivative of urushiol as the main monomer for polymerization in dentin adhesive and its effect on hydrolysis resistance. The derivative was characterized by Fourier transform infrared spectroscopy and (1)H nuclear magnetic resonance spectroscopy. Compared with the Adper Single Bond 2, the experimentally synthesized adhesives had higher contact angles. In particular, the water sorption/solubility of the experimental samples were significantly lower than that of Adper Single Bond 2. The microtensile bond strengths of the test groups were higher than that of the control group, even after 5000 thermocycles. Cytotoxicity test results showed that adhesives based on the original derivative induced low toxicity to L929 cells. The results of this study may shift the focus of future research to natural monomers and even their derivatives which may perform well in dentistry. The Royal Society of Chemistry 2021-05-21 /pmc/articles/PMC9033433/ /pubmed/35480923 http://dx.doi.org/10.1039/d1ra00471a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhao, Ying
He, Xi
Wang, Han
Zhu, Jiufu
Wang, Huimin
Zheng, Yan
Zhu, Song
Cui, Zhanchen
Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title_full Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title_fullStr Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title_full_unstemmed Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title_short Synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
title_sort synthesis of an urushiol derivative and its use for hydrolysis resistance in dentin adhesive
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033433/
https://www.ncbi.nlm.nih.gov/pubmed/35480923
http://dx.doi.org/10.1039/d1ra00471a
work_keys_str_mv AT zhaoying synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT hexi synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT wanghan synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT zhujiufu synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT wanghuimin synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT zhengyan synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT zhusong synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive
AT cuizhanchen synthesisofanurushiolderivativeanditsuseforhydrolysisresistanceindentinadhesive