Tetrahydrocurcumin encapsulation in ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Tetrahydrocurcumin encapsulation in cyclodextrins for water solubility improvement: synthesis, characterization and antifungal activity as a new biofungicide
Auteur(s) :
Loron, Anne [Auteur]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Gardrat, Christian [Auteur]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Tabary, Nicolas [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Martel, Bernard [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Coma, Véronique [Auteur]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Gardrat, Christian [Auteur]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Tabary, Nicolas [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Martel, Bernard [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Coma, Véronique [Auteur]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Titre de la revue :
Carbohydrate Polymer Technologies and Applications
Pagination :
100113
Éditeur :
Elsevier BV
Date de publication :
2021-07-03
Statut de l’article :
À paraître
ISSN :
2666-8939
Mot(s)-clé(s) en anglais :
Cyclodextrins tetrahydrocurcumin encapsulation
methylated β-cyclodextrin
F. graminearum
antifungal activity
methylated β-cyclodextrin
F. graminearum
antifungal activity
Discipline(s) HAL :
Chimie/Matériaux
Chimie/Polymères
Chimie/Polymères
Résumé en anglais : [en]
The solubility of the scarcely water-soluble molecule tetrahydrocurcumin (THC), a promising curcumin derivative to be used as biopesticide, was enhanced through the formation of inclusion complexes with different cyclodextrins ...
Lire la suite >The solubility of the scarcely water-soluble molecule tetrahydrocurcumin (THC), a promising curcumin derivative to be used as biopesticide, was enhanced through the formation of inclusion complexes with different cyclodextrins (CDs). Randomly methylated β-cyclodextrin (MeβCD) gave the best results among the different CDs whose size, substituent or structure was changing. Differential scanning calorimetry as well as 1H- and 2D-Nuclear Magnetic Resonance (NMR) proved the inclusion of THC in MeβCD. Rotating-frame Overhauser effect spectroscopy NMR especially illustrated specific interactions of aromatic protons of THC and protons located inside the CD cavity. The complex formation between THC and MeβCD was studied using the Higuchi and Connor method, giving an association constant of 591 M−1. THC-loaded MeβCD did not show any growth inhibition of the target fungus Fusarium graminearum. However, THC-loaded MeβCD polymers exhibited 25 % inhibition of the fungal growth, thus making them promising material for solvent-free, aqueous and bio-based fungicide formulations.Lire moins >
Lire la suite >The solubility of the scarcely water-soluble molecule tetrahydrocurcumin (THC), a promising curcumin derivative to be used as biopesticide, was enhanced through the formation of inclusion complexes with different cyclodextrins (CDs). Randomly methylated β-cyclodextrin (MeβCD) gave the best results among the different CDs whose size, substituent or structure was changing. Differential scanning calorimetry as well as 1H- and 2D-Nuclear Magnetic Resonance (NMR) proved the inclusion of THC in MeβCD. Rotating-frame Overhauser effect spectroscopy NMR especially illustrated specific interactions of aromatic protons of THC and protons located inside the CD cavity. The complex formation between THC and MeβCD was studied using the Higuchi and Connor method, giving an association constant of 591 M−1. THC-loaded MeβCD did not show any growth inhibition of the target fungus Fusarium graminearum. However, THC-loaded MeβCD polymers exhibited 25 % inhibition of the fungal growth, thus making them promising material for solvent-free, aqueous and bio-based fungicide formulations.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
INRA
ENSCL
CNRS
INRA
ENSCL
Collections :
Équipe(s) de recherche :
Ingénierie des Systèmes Polymères
Date de dépôt :
2021-07-05T12:06:15Z
2021-07-06T13:14:26Z
2021-07-06T13:14:26Z