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spelling paper:paper_00225142_v91_n14_p2551_dosSantos2023-06-08T14:51:20Z Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes Buera, María del Pilar Mazzobre, María Florencia Cholesterol Cyclodextrin Phase solubility Stability constants beta cyclodextrin derivative cholesterol coordination compound food additive ligand phytosterol water adsorption article chemical phenomena chemistry diet supplementation differential scanning calorimetry food handling freeze drying heat kinetics phase transition solubility Adsorption beta-Cyclodextrins Calorimetry, Differential Scanning Cholesterol Coordination Complexes Food Additives Food Handling Food, Fortified Freeze Drying Hot Temperature Hydrophobic and Hydrophilic Interactions Kinetics Ligands Phase Transition Phytosterols Solubility Water Background: Cyclodextrins (CDs) are able to enhance the solubility, stability and bioavailability of several bioactive hydrophobic compounds by complex formation. They can also be used for removal of undesired components (such as cholesterol, off-flavors or bitter components) present in foods. Although many patents account for the use of cyclodextrins for removal of cholesterol from dairy foods, there is no available information on the effect of water on encapsulation efficiency and on the stability of sterols in CDs. The aim of this work was to study the inclusion properties and the factors affecting the encapsulation and stability of cholesterol in β-cyclodextrin (BCD). The optimum encapsulation conditions (ligand-CD molar ratio, stirring time and temperature), and stability of the complexes as a function of storage time and water content were analyzed. Results: Phase solubility study pointed out the formation of 1:1 stoichiometric complexes between cholesterol and β-cyclodextrin, which was influenced by temperature variations. The process was shown to be exothermic and energetically favored. The presence of cholesterol greatly modified the BCD water sorption curves, being the amount of adsorbed water smaller in the combined systems. The principal 'driving force' for complex formation is the substitution of the high-enthalpy water molecules by an appropriate hydrophobic ligand. The freeze-dried complexes probed to be stable at different storage conditions. Conclusion: The phase solubility and stability data obtained could be essential for selecting the most suitable conditions when CDs are employed either for removing cholesterol or to incorporate functional ingredients (i.e. sitosterol) in the development of innovative food products. © 2011 Society of Chemical Industry. Fil:Buera, M.P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Mazzobre, M.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00225142_v91_n14_p2551_dosSantos http://hdl.handle.net/20.500.12110/paper_00225142_v91_n14_p2551_dosSantos
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cholesterol
Cyclodextrin
Phase solubility
Stability constants
beta cyclodextrin derivative
cholesterol
coordination compound
food additive
ligand
phytosterol
water
adsorption
article
chemical phenomena
chemistry
diet supplementation
differential scanning calorimetry
food handling
freeze drying
heat
kinetics
phase transition
solubility
Adsorption
beta-Cyclodextrins
Calorimetry, Differential Scanning
Cholesterol
Coordination Complexes
Food Additives
Food Handling
Food, Fortified
Freeze Drying
Hot Temperature
Hydrophobic and Hydrophilic Interactions
Kinetics
Ligands
Phase Transition
Phytosterols
Solubility
Water
spellingShingle Cholesterol
Cyclodextrin
Phase solubility
Stability constants
beta cyclodextrin derivative
cholesterol
coordination compound
food additive
ligand
phytosterol
water
adsorption
article
chemical phenomena
chemistry
diet supplementation
differential scanning calorimetry
food handling
freeze drying
heat
kinetics
phase transition
solubility
Adsorption
beta-Cyclodextrins
Calorimetry, Differential Scanning
Cholesterol
Coordination Complexes
Food Additives
Food Handling
Food, Fortified
Freeze Drying
Hot Temperature
Hydrophobic and Hydrophilic Interactions
Kinetics
Ligands
Phase Transition
Phytosterols
Solubility
Water
Buera, María del Pilar
Mazzobre, María Florencia
Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
topic_facet Cholesterol
Cyclodextrin
Phase solubility
Stability constants
beta cyclodextrin derivative
cholesterol
coordination compound
food additive
ligand
phytosterol
water
adsorption
article
chemical phenomena
chemistry
diet supplementation
differential scanning calorimetry
food handling
freeze drying
heat
kinetics
phase transition
solubility
Adsorption
beta-Cyclodextrins
Calorimetry, Differential Scanning
Cholesterol
Coordination Complexes
Food Additives
Food Handling
Food, Fortified
Freeze Drying
Hot Temperature
Hydrophobic and Hydrophilic Interactions
Kinetics
Ligands
Phase Transition
Phytosterols
Solubility
Water
description Background: Cyclodextrins (CDs) are able to enhance the solubility, stability and bioavailability of several bioactive hydrophobic compounds by complex formation. They can also be used for removal of undesired components (such as cholesterol, off-flavors or bitter components) present in foods. Although many patents account for the use of cyclodextrins for removal of cholesterol from dairy foods, there is no available information on the effect of water on encapsulation efficiency and on the stability of sterols in CDs. The aim of this work was to study the inclusion properties and the factors affecting the encapsulation and stability of cholesterol in β-cyclodextrin (BCD). The optimum encapsulation conditions (ligand-CD molar ratio, stirring time and temperature), and stability of the complexes as a function of storage time and water content were analyzed. Results: Phase solubility study pointed out the formation of 1:1 stoichiometric complexes between cholesterol and β-cyclodextrin, which was influenced by temperature variations. The process was shown to be exothermic and energetically favored. The presence of cholesterol greatly modified the BCD water sorption curves, being the amount of adsorbed water smaller in the combined systems. The principal 'driving force' for complex formation is the substitution of the high-enthalpy water molecules by an appropriate hydrophobic ligand. The freeze-dried complexes probed to be stable at different storage conditions. Conclusion: The phase solubility and stability data obtained could be essential for selecting the most suitable conditions when CDs are employed either for removing cholesterol or to incorporate functional ingredients (i.e. sitosterol) in the development of innovative food products. © 2011 Society of Chemical Industry.
author Buera, María del Pilar
Mazzobre, María Florencia
author_facet Buera, María del Pilar
Mazzobre, María Florencia
author_sort Buera, María del Pilar
title Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
title_short Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
title_full Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
title_fullStr Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
title_full_unstemmed Phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
title_sort phase solubility studies and stability of cholesterol/β-cyclodextrin inclusion complexes
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00225142_v91_n14_p2551_dosSantos
http://hdl.handle.net/20.500.12110/paper_00225142_v91_n14_p2551_dosSantos
work_keys_str_mv AT bueramariadelpilar phasesolubilitystudiesandstabilityofcholesterolbcyclodextrininclusioncomplexes
AT mazzobremariaflorencia phasesolubilitystudiesandstabilityofcholesterolbcyclodextrininclusioncomplexes
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