Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes

The water sorption and physical properties of freeze-dried β-cyclodextrin (BCD) and 2-hydroxypropyl-β-cyclodextrin (HBCD) were studied. The stability of the inclusion complexes of these cyclodextrins with different hydrophobic ingredients, such as myristic acid and α-terpineol, was investigated as a...

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Autores principales: Dos Santos, C., Buera, M.P., Mazzobre, M.F.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03088146_v132_n4_p2030_DosSantos
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spelling todo:paper_03088146_v132_n4_p2030_DosSantos2023-10-03T15:22:54Z Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes Dos Santos, C. Buera, M.P. Mazzobre, M.F. α-Terpineol Freeze-dried complexes Hydroxypropyl-β-cyclodextrin Myristic acid Physical properties Water sorption CdS Freeze-dried complexes Hydrocarbon chains Inclusion complex Inner cavities Ligand structure Myristic acid Non-polar ligands Sorption properties Storage time Transition values Water adsorption Water interactions Water molecule Water sorption Adsorption Cyclodextrins Glass transition Hydrates Hydrocarbons Ligands Physical properties Saturated fatty acids Dewatering 2 hydroxypropyl beta cyclodextrin beta cyclodextrin derivative myristic acid terpineol water adsorption chemical structure complex formation conference paper encapsulation glass transition temperature solubility time water absorption water content The water sorption and physical properties of freeze-dried β-cyclodextrin (BCD) and 2-hydroxypropyl-β-cyclodextrin (HBCD) were studied. The stability of the inclusion complexes of these cyclodextrins with different hydrophobic ingredients, such as myristic acid and α-terpineol, was investigated as a function of the storage time and water content of the systems. Besides increasing its solubility, BCD ring modification with hydroxypropyl groups conferred amorficity to the dehydrated matrices, and modified the sorption properties and their ability to form hydrates. Both ligands decreased BCD and HBCD water adsorption, in comparison with the pure cyclodextrins. The water adsorption data and glass transition values obtained are consistent with the displacement of water molecules from the inner cavity of the CDs when the ligand is included. Encapsulation of non-polar ligands of linear hydrocarbon chain, like myristic acid, was initially incomplete, depending on the ligand/CD ratio, and increased with the time of storage and water content. © 2011 Elsevier Ltd. All rights reserved. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03088146_v132_n4_p2030_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 α-Terpineol
Freeze-dried complexes
Hydroxypropyl-β-cyclodextrin
Myristic acid
Physical properties
Water sorption
CdS
Freeze-dried complexes
Hydrocarbon chains
Inclusion complex
Inner cavities
Ligand structure
Myristic acid
Non-polar ligands
Sorption properties
Storage time
Transition values
Water adsorption
Water interactions
Water molecule
Water sorption
Adsorption
Cyclodextrins
Glass transition
Hydrates
Hydrocarbons
Ligands
Physical properties
Saturated fatty acids
Dewatering
2 hydroxypropyl beta cyclodextrin
beta cyclodextrin derivative
myristic acid
terpineol
water
adsorption
chemical structure
complex formation
conference paper
encapsulation
glass transition temperature
solubility
time
water absorption
water content
spellingShingle α-Terpineol
Freeze-dried complexes
Hydroxypropyl-β-cyclodextrin
Myristic acid
Physical properties
Water sorption
CdS
Freeze-dried complexes
Hydrocarbon chains
Inclusion complex
Inner cavities
Ligand structure
Myristic acid
Non-polar ligands
Sorption properties
Storage time
Transition values
Water adsorption
Water interactions
Water molecule
Water sorption
Adsorption
Cyclodextrins
Glass transition
Hydrates
Hydrocarbons
Ligands
Physical properties
Saturated fatty acids
Dewatering
2 hydroxypropyl beta cyclodextrin
beta cyclodextrin derivative
myristic acid
terpineol
water
adsorption
chemical structure
complex formation
conference paper
encapsulation
glass transition temperature
solubility
time
water absorption
water content
Dos Santos, C.
Buera, M.P.
Mazzobre, M.F.
Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
topic_facet α-Terpineol
Freeze-dried complexes
Hydroxypropyl-β-cyclodextrin
Myristic acid
Physical properties
Water sorption
CdS
Freeze-dried complexes
Hydrocarbon chains
Inclusion complex
Inner cavities
Ligand structure
Myristic acid
Non-polar ligands
Sorption properties
Storage time
Transition values
Water adsorption
Water interactions
Water molecule
Water sorption
Adsorption
Cyclodextrins
Glass transition
Hydrates
Hydrocarbons
Ligands
Physical properties
Saturated fatty acids
Dewatering
2 hydroxypropyl beta cyclodextrin
beta cyclodextrin derivative
myristic acid
terpineol
water
adsorption
chemical structure
complex formation
conference paper
encapsulation
glass transition temperature
solubility
time
water absorption
water content
description The water sorption and physical properties of freeze-dried β-cyclodextrin (BCD) and 2-hydroxypropyl-β-cyclodextrin (HBCD) were studied. The stability of the inclusion complexes of these cyclodextrins with different hydrophobic ingredients, such as myristic acid and α-terpineol, was investigated as a function of the storage time and water content of the systems. Besides increasing its solubility, BCD ring modification with hydroxypropyl groups conferred amorficity to the dehydrated matrices, and modified the sorption properties and their ability to form hydrates. Both ligands decreased BCD and HBCD water adsorption, in comparison with the pure cyclodextrins. The water adsorption data and glass transition values obtained are consistent with the displacement of water molecules from the inner cavity of the CDs when the ligand is included. Encapsulation of non-polar ligands of linear hydrocarbon chain, like myristic acid, was initially incomplete, depending on the ligand/CD ratio, and increased with the time of storage and water content. © 2011 Elsevier Ltd. All rights reserved.
format JOUR
author Dos Santos, C.
Buera, M.P.
Mazzobre, M.F.
author_facet Dos Santos, C.
Buera, M.P.
Mazzobre, M.F.
author_sort Dos Santos, C.
title Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
title_short Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
title_full Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
title_fullStr Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
title_full_unstemmed Influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
title_sort influence of ligand structure and water interactions on the physical properties of β-cyclodextrins complexes
url http://hdl.handle.net/20.500.12110/paper_03088146_v132_n4_p2030_DosSantos
work_keys_str_mv AT dossantosc influenceofligandstructureandwaterinteractionsonthephysicalpropertiesofbcyclodextrinscomplexes
AT bueramp influenceofligandstructureandwaterinteractionsonthephysicalpropertiesofbcyclodextrinscomplexes
AT mazzobremf influenceofligandstructureandwaterinteractionsonthephysicalpropertiesofbcyclodextrinscomplexes
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