Competitive Binding of Aroma Compounds by β-Cyclodextrin
Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and β-cyclodextrin. A maximal retention of a mole of aroma per mole of β-cyclodextrin has been observed for five of the aroma compounds, whereas retention of benzyl alcohol can be twice as high. Re...
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Published in | Journal of agricultural and food chemistry Vol. 49; no. 12; pp. 5916 - 5922 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Washington, DC
American Chemical Society
01.12.2001
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Abstract | Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and β-cyclodextrin. A maximal retention of a mole of aroma per mole of β-cyclodextrin has been observed for five of the aroma compounds, whereas retention of benzyl alcohol can be twice as high. Retention of a mixture of aroma compounds has also been studied. It has been noted that when volatile compounds compete for the same binding sites on β-cyclodextrin, ethyl hexanoate, 2-methylbutyric acid, and benzyl alcohol are, respectively, better retained than ethyl propionate, hexanoic acid, and hexanol. Preferential retention observed with esters can be simply explained by their difference of physicochemical properties, but for the acids and alcohols a study at the molecular scale has been necessary. The better retention of 2-methylbutyric acid can be explained by differences in the nature of interaction between the acids and their carrier. At least selectivity of retention noted for the alcohol could be due to a difference in the location of the guest and also a difference in the number of aroma molecules that can be bound per polysaccharide molecule. Keywords: Aroma; encapsulation; competition; β-cyclodextrinn; interaction; NMR |
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AbstractList | Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and beta-cyclodextrin. A maximal retention of a mole of aroma per mole of beta-cyclodextrin has been observed for five of the aroma compounds, whereas retention of benzyl alcohol can be twice as high. Retention of a mixture of aroma compounds has also been studied. It has been noted that when volatile compounds compete for the same binding sites on beta-cyclodextrin, ethyl hexanoate, 2-methylbutyric acid, and benzyl alcohol are, respectively, better retained than ethyl propionate, hexanoic acid, and hexanol. Preferential retention observed with esters can be simply explained by their difference of physicochemical properties, but for the acids and alcohols a study at the molecular scale has been necessary. The better retention of 2-methylbutyric acid can be explained by differences in the nature of interaction between the acids and their carrier. At least selectivity of retention noted for the alcohol could be due to a difference in the location of the guest and also a difference in the number of aroma molecules that can be bound per polysaccharide molecule. Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and β-cyclodextrin. A maximal retention of a mole of aroma per mole of β-cyclodextrin has been observed for five of the aroma compounds, whereas retention of benzyl alcohol can be twice as high. Retention of a mixture of aroma compounds has also been studied. It has been noted that when volatile compounds compete for the same binding sites on β-cyclodextrin, ethyl hexanoate, 2-methylbutyric acid, and benzyl alcohol are, respectively, better retained than ethyl propionate, hexanoic acid, and hexanol. Preferential retention observed with esters can be simply explained by their difference of physicochemical properties, but for the acids and alcohols a study at the molecular scale has been necessary. The better retention of 2-methylbutyric acid can be explained by differences in the nature of interaction between the acids and their carrier. At least selectivity of retention noted for the alcohol could be due to a difference in the location of the guest and also a difference in the number of aroma molecules that can be bound per polysaccharide molecule. Keywords: Aroma; encapsulation; competition; β-cyclodextrinn; interaction; NMR |
Author | Guichard, E Dahout, C Goubet, I Le Quéré, J.-L Sémon, E Voilley, A |
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Cites_doi | 10.1006/fstl.1994.1107 10.1246/bcsj.31.1081 10.1021/ja00294a021 10.1111/j.1365-2621.1986.tb11224.x 10.1111/j.1365-2621.1997.tb15037.x 10.1042/bst0110136 10.1021/jf00095a030 10.1016/0308-8146(92)90226-R 10.1080/10601329608010886 10.1021/i160065a009 10.1021/bk-1995-0590 10.1295/polymj.28.91 10.1080/10408399309527645 10.1021/jf00125a056 10.1007/978-94-009-7855-3_49 10.1051/jcp/1993900545 |
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Keywords | Volatile compound Encapsulation Oligosaccharide Organoleptic properties Binding site Dehydration Retention Flavor Competitive fixation Cyclodextrin Cyclic compound Molecular competition Aroma Comparative study BETA-CYCLODEXTRINE |
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Snippet | Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and β-cyclodextrin. A maximal retention of a mole of... Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and beta-cyclodextrin. A maximal retention of a mole of... Retention of six aroma compounds has been studied after dehydration of ternary mixtures of aroma water and beta -cyclodextrin. A maximal retention of a mole of... |
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SubjectTerms | Alcohols - chemistry Aroma and flavouring agent industries beta-Cyclodextrins Binding, Competitive Biological and medical sciences Carboxylic Acids - chemistry Cyclodextrins - chemistry Esters - chemistry Food engineering Food industries Freeze Drying Fundamental and applied biological sciences. Psychology Kinetics Life Sciences Odorants - analysis |
Title | Competitive Binding of Aroma Compounds by β-Cyclodextrin |
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