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1. (Article ID: 12676)
Selim K, Tsimidou M, Biliaderis CG
Kinetic studies of degradation of saffron carotenoids encapsulated in amorphous polymer matrices
Food Chemistry 71(2) (2000)
199-206
Kinetic studies on degradation of saffron water soluble carotenoids (mainly crocins) encapsulated in three different amorphous matrices (pullulan and two polyvinylpyrrolidone, PVP, samples differing in their molecular weight) were carried out at different water activity (aw) conditions (0.43, 0.53, 0.64 and 0.75) in the dark at 35°C. Degradation of the polar pigments was monitored by periodic measurements of the coloring strength. Among the polymeric matrices used as wall materials, which largely decreased the oxidation rates of crocetin glycosides, PVP 40 was the most effective carrier under all storage conditions. In the vicinity of the glass transition temperature (Tg) zone, where pullulan and PVP360 undergo state transformations, there was a change in the reaction rate. The lower degradation rates were observed for PVP40 under conditions where this matrix was fully plasticized (i.e. rubbery) and “collapsed”, implying that the degradation kinetics are not governed by factors related to the physical state and molecular mobility of the inert matrix. Carotenoid losses have been observed even at temperatures below the Tg of the polymeric matrices.
saffron; crocins; degradation; encapsulation; glass transition temperature
Publication DOI: 10.1016/S0308-8146(00)00156-4Journal NLM ID: 7702639Publisher: Elsevier Applied Science Publishers
Correspondence: biliader

agro.auth.gr
Institutions: Mediterranean Agronomic Institute of Chania (MAICH), Alsillion Agrokipiou, Chania, Greece, Laboratory of Food Chemistry and Technology, Faculty of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece, Department of Food Science and Technology, School of Agriculture, Aristotle University of Thessaloniki, Thessaloniki, Greece
The publication contains the following compound(s):
- Compound ID: 29150
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-+
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-16)-Subst
Subst = all-trans-crocetin = SMILES C/C(=C\C=C\C=C(C)\C=C\C=C(C)\{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Trivial name: all-trans-digentiobiosyl crocin, crocin
Compound class: glycoside, carotenoid
- Compound ID: 29151
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-+
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-16)-Subst
Subst = 13-cis-crocetin = SMILES C/C(=C\C=C\C=C(C)/C=C/C=C(C)/{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Trivial name: 13-cis-gentiobiosyl glycosyl crocin
Compound class: glycoside, carotenoid
- Compound ID: 29879
|
b-D-Glcp-(1-16)-+
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-Subst
Subst = all-trans-crocetin = SMILES C/C(=C\C=C\C=C(C)\C=C\C=C(C)\{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Compound class: glycoside, carotenoid
- Compound ID: 31478
|
b-D-Glcp-(1-1)-+
|
b-D-Glcp-(1-16)-Subst
Subst = all-trans-crocetin = SMILES C/C(=C\C=C\C=C(C)\C=C\C=C(C)\{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Compound class: glycoside, carotenoid
- Compound ID: 31479
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-Subst
Subst = all-trans-crocetin = SMILES C/C(=C\C=C\C=C(C)\C=C\C=C(C)\{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Trivial name: crocin
Compound class: glycoside, carotenoid
- Compound ID: 32882
|
b-D-Glcp-(1-16)-+
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-Subst
Subst = 13-cis-crocetin = SMILES C/C(=C\C=C\C=C(C)/C=C/C=C(C)/{1}C(=O)O)/C=C/C=C(C)/{16}C(=O)O |
Show graphically |
Structure type: oligomer
Compound class: glycoside, carotenoid
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