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Preparation of Hop Estrogen-Active Material for Production of Food Supplements
M. Karabín, T. Haimannová, K. Fialová, L. Jelínek, P. Dostálek
Language English Country Switzerland
Document type Journal Article
Grant support
TE02000177
Technology Agency of the Czech Republic
NLK
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- MeSH
- Flavanones chemistry metabolism MeSH
- Flavonoids chemistry metabolism MeSH
- Phytoestrogens chemistry metabolism MeSH
- Humulus chemistry MeSH
- Catalysis MeSH
- Humans MeSH
- Magnesium Oxide chemistry metabolism MeSH
- Beer analysis MeSH
- Dietary Supplements analysis MeSH
- Propiophenones chemistry metabolism MeSH
- Plant Extracts metabolism MeSH
- Plant Preparations chemistry metabolism MeSH
- Temperature MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
In recent years, the interest in the health-promoting effects of hop prenylflavonoids, especially its estrogenic effects, has grown. Unfortunately, one of the most potent phytoestrogens identified so far, 8-prenylnaringenin, is only a minor component of hops, so its isolation from hop materials for the production of estrogenically active food supplements has proved to be problematic. The aim of this study was to optimize the conditions (e.g., temperature, the length of the process and the amount of the catalyst) to produce 8-prenylnaringenin-rich material by the magnesium oxide-catalyzed thermal isomerization of desmethylxanthohumol. Under these optimized conditions, the yield of 8-prenylnaringenin was 29 mg per 100 gDW of product, corresponding to a >70% increase in its content relative to the starting material. This process may be applied in the production of functional foods or food supplements rich in 8-prenylnaringenin, which may then be utilized in therapeutic agents to help alleviate the symptoms of menopausal disorders.
References provided by Crossref.org
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- $a In recent years, the interest in the health-promoting effects of hop prenylflavonoids, especially its estrogenic effects, has grown. Unfortunately, one of the most potent phytoestrogens identified so far, 8-prenylnaringenin, is only a minor component of hops, so its isolation from hop materials for the production of estrogenically active food supplements has proved to be problematic. The aim of this study was to optimize the conditions (e.g., temperature, the length of the process and the amount of the catalyst) to produce 8-prenylnaringenin-rich material by the magnesium oxide-catalyzed thermal isomerization of desmethylxanthohumol. Under these optimized conditions, the yield of 8-prenylnaringenin was 29 mg per 100 gDW of product, corresponding to a >70% increase in its content relative to the starting material. This process may be applied in the production of functional foods or food supplements rich in 8-prenylnaringenin, which may then be utilized in therapeutic agents to help alleviate the symptoms of menopausal disorders.
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