## Abstract Numerous studies have demonstrated the potential of isoflavones occurring in soy (__Glycine max__ L.) and red clover (__Trifolium pratense__ L.) to alleviate climacteric complaints. They have also shown beneficial effects on the cardiovascular system and in the prevention of osteoporosi
Thermal degradation kinetics of isoflavone aglycones from soy and red clover
β Scribed by Florian Conrad Stintzing; Manuel Hoffmann; Reinhold Carle
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 664 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1613-4125
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β¦ Synopsis
Abstract
Driven by their beneficial effects on human metabolism, isoflavonoids have gained considerable importance reflected by an increased number of isoflavoneβrich foods, food supplements and pharmaceutical products on the market, mainly derived from soy and red clover. While it is well known that the genuine isoflavone pattern will be altered during processing, data on aglycone stability are rare. Therefore, a thorough study into the thermal sensitivities of biochanin A, daidzein, formononetin, flavone, genistein, glycitein and isoflavone was performed. Samples were heated at 150Β°C over a period of 7 h at three different pH values, and degradation of the aglycones was monitored by HPLCβDAD analyses. Therefrom, structureβrelated stability characteristics could be established. While virtually no decay was observed at pH 7.0 and 5.6, degradation was most prominent at pH 3. 1. Individual aglycone retention was further dependent on heating time with daidzein being the most labile compound after any time interval. Curve fitting of the data revealed firstβorder degradation kinetics for flavone and glycitein, while the remaining aglycones exhibited a sigmoidal degradation pattern.
π SIMILAR VOLUMES
Thermal degradation of polydimethylsiloxane (PDMS) polymers having hydroxyl (PS) and vinyl (PS-V) terminals was studied by pyrolysis-gas chromatography (PGC) in the temperature range from 550 to 950Β°C. The degradation products were primarily cyclic oligomers ranging from trimer (D 3 ) to cyclomer D