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 inJournal of agricultural and food chemistry Vol. 49; no. 12; pp. 5916 - 5922
Main Authors Goubet, I, Dahout, C, Sémon, E, Guichard, E, Le Quéré, J.-L, Voilley, A
Format Journal Article
LanguageEnglish
Published 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
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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Issue 12
Keywords Volatile compound
Encapsulation
Oligosaccharide
Organoleptic properties
Binding site
Dehydration
Retention
Flavor
Competitive fixation
Cyclodextrin
Cyclic compound
Molecular competition
Aroma
Comparative study
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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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StartPage 5916
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
URI http://dx.doi.org/10.1021/jf0101049
https://api.istex.fr/ark:/67375/TPS-2M2J01HS-V/fulltext.pdf
https://www.ncbi.nlm.nih.gov/pubmed/11743785
https://search.proquest.com/docview/18433569
https://hal.inrae.fr/hal-02671836
Volume 49
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