Evidence map›Paper›PMID 35465773›Full record

ArticleToxicology and industrial health2022

Nature-derived epoxy resins: Synthesis, allergenicity, and thermosetting properties of pinoresinol diglycidyl ether.

Niamh M O'Boyle, Ida B Niklasson, David J Ponting, Miguel A Ortega, Tina Seifert, Andreas Natsch, Kristina Luthman, Ann-Therese Karlberg

Open access · hybridAbstract read
In one paragraph

Article in Toxicology and industrial health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Niamh M O'BoyleDepartment of Chemistry and Molecular Biology, Dermatochemistry and Skin Allergy, 3570University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0001-5660-4944
Ida B NiklassonDepartment of Chemistry and Molecular Biology, Dermatochemistry and Skin Allergy, 3570University of Gothenburg, Gothenburg, Sweden.
David J PontingDepartment of Chemistry and Molecular Biology, Dermatochemistry and Skin Allergy, 3570University of Gothenburg, Gothenburg, Sweden.
Miguel A OrtegaDepartment of Chemistry and Molecular Biology, Dermatochemistry and Skin Allergy, 3570University of Gothenburg, Gothenburg, Sweden.
Tina SeifertDepartment of Chemistry and Molecular Biology, Medicinal Chemistry, 3570University of Gothenburg, Gothenburg, Sweden.
Andreas Natsch118530Givaudan Schweiz AG, Duebendorf, Switzerland.
Kristina LuthmanDepartment of Chemistry and Molecular Biology, Medicinal Chemistry, 3570University of Gothenburg, Gothenburg, Sweden.
Ann-Therese KarlbergDepartment of Chemistry and Molecular Biology, Dermatochemistry and Skin Allergy, 3570University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0003-2691-3644
University of Gothenburg · SEGivaudan (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a novel nature-derived epoxy resin monomer (ERM) derived from the plant lignan pinoresinol. Epoxy resins are thermosetting materials in global usage owing to their excellent technical properties such as flexibility and durability. However, their adverse health effects are often not considered and affect users of epoxy resins worldwide. Components of epoxy resin systems are strong skin sensitizers and cause allergic contact dermatitis. The reported prevalence attributable to epoxy chemicals is between 11.7 and 12.5% of all cases of occupational allergic contact dermatitis. We are committed to developing epoxy resins with reduced allergenic effect, while maintaining their excellent properties. The novel ERM, pinoresinol diglycidyl ether (PinoDGE), was synthesized in one step from pinoresinol and epichlorohydrin in 88% yield. It was not classified as a skin sensitizer in the in vivo local lymph node assay, at concentrations up to 0.17 m, as it did not cause a stimulation index >3 compared to control. Pinoresinol diglycidyl ether reacted with the model peptide AcPHCKRM in a reactivity assay and was predicted to be a skin sensitizer in the KeratinoSens assay. Preliminary cross-linking studies indicate that it has promising properties compared to commercially used ERMs. Pinoresinol diglycidyl ether could be seen as a lead compound for further development of alternative ERMs with a better safety profile based on natural and renewable sources for construction of epoxy resin polymers.

Indexed as

Dermatitis, Allergic ContactLignansAllergensBenzhydryl CompoundsEpoxy CompoundsEpoxy ResinsFuransHumansAllergensBenzhydryl CompoundsEpoxy CompoundsEpoxy ResinsFuransLignanspinoresinolcontact allergyepoxidesEpoxy resinsoccupational contact dermatitispinoresinolskin

Identifiers

PMID35465773
PMCPMC9082971
OpenAlexW4224326172

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.