Cargando…
Nature-Derived Epoxy Resin Monomers with Reduced Sensitizing Capacity—Isosorbide-Based Bis-Epoxides
[Image: see text] Epoxy resin systems (ERSs) are a class of thermosetting resins that become thermostable and insoluble polymers upon curing. They are widely used as components of protective surfaces, adhesives, and paints and in the manufacturing of composites in the plastics industry. The diglycid...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945177/ https://www.ncbi.nlm.nih.gov/pubmed/36652206 http://dx.doi.org/10.1021/acs.chemrestox.2c00347 |
_version_ | 1784892081006706688 |
---|---|
author | Karlsson, Isabella Ponting, David J. Ortega, Miguel A. Niklasson, Ida B. Ndreu, Lorena Stéen, E. Johanna L. Seifert, Tina Luthman, Kristina Karlberg, Ann-Therese |
author_facet | Karlsson, Isabella Ponting, David J. Ortega, Miguel A. Niklasson, Ida B. Ndreu, Lorena Stéen, E. Johanna L. Seifert, Tina Luthman, Kristina Karlberg, Ann-Therese |
author_sort | Karlsson, Isabella |
collection | PubMed |
description | [Image: see text] Epoxy resin systems (ERSs) are a class of thermosetting resins that become thermostable and insoluble polymers upon curing. They are widely used as components of protective surfaces, adhesives, and paints and in the manufacturing of composites in the plastics industry. The diglycidyl ether of bisphenol A (DGEBA) is used in 75–90% of ERSs and is thus by far the most used epoxy resin monomer (ERM). Unfortunately, DGEBA is a strong skin sensitizer and it is one of the most common causes of occupational contact dermatitis. Furthermore, DGEBA is synthesized from bisphenol A (BPA), which is a petroleum-derived chemical with endocrine-disruptive properties. In this work, we have used isosorbide, a renewable and nontoxic sugar-based material, as an alternative to BPA in the design of ERMs. Three different bis-epoxide isosorbide derivatives were synthesized: the diglycidyl ether of isosorbide (1) and two novel isosorbide-based bis-epoxides containing either a benzoic ester (2) or a benzyl ether linkage (3). Assessment of the in vivo sensitizing potency of the isosorbide bis-epoxides in the murine local lymph node assay (LLNA) showed that all three compounds were significantly less sensitizing than DGEBA, especially 2 which was nonsensitizing up to 25% w/v. The peptide reactivity showed the same order of reactivity as the LLNA, i.e., 2 being the least reactive, followed by 3 and then 1, which displayed similar peptide reactivity as DGEBA. Skin permeation of 2 and 3 was compared to DGEBA using ex vivo pig skin and static Franz cells. The preliminary investigations of the technical properties of the polymers formed from 1–3 were promising. Although further investigations of the technical properties are needed, all isosorbide bis-epoxides have the potential to be less sensitizing renewable replacements of DGEBA, especially 2 that had the lowest sensitizing potency in vivo as well as the lowest peptide reactivity. |
format | Online Article Text |
id | pubmed-9945177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99451772023-02-23 Nature-Derived Epoxy Resin Monomers with Reduced Sensitizing Capacity—Isosorbide-Based Bis-Epoxides Karlsson, Isabella Ponting, David J. Ortega, Miguel A. Niklasson, Ida B. Ndreu, Lorena Stéen, E. Johanna L. Seifert, Tina Luthman, Kristina Karlberg, Ann-Therese Chem Res Toxicol [Image: see text] Epoxy resin systems (ERSs) are a class of thermosetting resins that become thermostable and insoluble polymers upon curing. They are widely used as components of protective surfaces, adhesives, and paints and in the manufacturing of composites in the plastics industry. The diglycidyl ether of bisphenol A (DGEBA) is used in 75–90% of ERSs and is thus by far the most used epoxy resin monomer (ERM). Unfortunately, DGEBA is a strong skin sensitizer and it is one of the most common causes of occupational contact dermatitis. Furthermore, DGEBA is synthesized from bisphenol A (BPA), which is a petroleum-derived chemical with endocrine-disruptive properties. In this work, we have used isosorbide, a renewable and nontoxic sugar-based material, as an alternative to BPA in the design of ERMs. Three different bis-epoxide isosorbide derivatives were synthesized: the diglycidyl ether of isosorbide (1) and two novel isosorbide-based bis-epoxides containing either a benzoic ester (2) or a benzyl ether linkage (3). Assessment of the in vivo sensitizing potency of the isosorbide bis-epoxides in the murine local lymph node assay (LLNA) showed that all three compounds were significantly less sensitizing than DGEBA, especially 2 which was nonsensitizing up to 25% w/v. The peptide reactivity showed the same order of reactivity as the LLNA, i.e., 2 being the least reactive, followed by 3 and then 1, which displayed similar peptide reactivity as DGEBA. Skin permeation of 2 and 3 was compared to DGEBA using ex vivo pig skin and static Franz cells. The preliminary investigations of the technical properties of the polymers formed from 1–3 were promising. Although further investigations of the technical properties are needed, all isosorbide bis-epoxides have the potential to be less sensitizing renewable replacements of DGEBA, especially 2 that had the lowest sensitizing potency in vivo as well as the lowest peptide reactivity. American Chemical Society 2023-01-18 /pmc/articles/PMC9945177/ /pubmed/36652206 http://dx.doi.org/10.1021/acs.chemrestox.2c00347 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Karlsson, Isabella Ponting, David J. Ortega, Miguel A. Niklasson, Ida B. Ndreu, Lorena Stéen, E. Johanna L. Seifert, Tina Luthman, Kristina Karlberg, Ann-Therese Nature-Derived Epoxy Resin Monomers with Reduced Sensitizing Capacity—Isosorbide-Based Bis-Epoxides |
title | Nature-Derived
Epoxy Resin Monomers with Reduced Sensitizing
Capacity—Isosorbide-Based Bis-Epoxides |
title_full | Nature-Derived
Epoxy Resin Monomers with Reduced Sensitizing
Capacity—Isosorbide-Based Bis-Epoxides |
title_fullStr | Nature-Derived
Epoxy Resin Monomers with Reduced Sensitizing
Capacity—Isosorbide-Based Bis-Epoxides |
title_full_unstemmed | Nature-Derived
Epoxy Resin Monomers with Reduced Sensitizing
Capacity—Isosorbide-Based Bis-Epoxides |
title_short | Nature-Derived
Epoxy Resin Monomers with Reduced Sensitizing
Capacity—Isosorbide-Based Bis-Epoxides |
title_sort | nature-derived
epoxy resin monomers with reduced sensitizing
capacity—isosorbide-based bis-epoxides |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945177/ https://www.ncbi.nlm.nih.gov/pubmed/36652206 http://dx.doi.org/10.1021/acs.chemrestox.2c00347 |
work_keys_str_mv | AT karlssonisabella naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT pontingdavidj naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT ortegamiguela naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT niklassonidab naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT ndreulorena naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT steenejohannal naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT seiferttina naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT luthmankristina naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides AT karlberganntherese naturederivedepoxyresinmonomerswithreducedsensitizingcapacityisosorbidebasedbisepoxides |