6533b829fe1ef96bd128a98b

RESEARCH PRODUCT

Structure of matrices based on pectin : formulation, characterization, functionality and controlled release during the encapsulation

Thi Diem Uyen Huynh

subject

Divalent cationsGelNaClMécanisme d’associationBinding mechanismCations divalentsPectinsStructureEncapsulationPectines[SDV.IDA] Life Sciences [q-bio]/Food engineering[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]

description

In this thesis, we studied the interactions between an anionic polysaccharide (pectin) and monovalent cation (Na+) and divalent cations (Ca2+, Zn2+, Ba2+, Mg2+) in dilute regime (c Ca2+ > Zn2+ > Mg2+; this may be related to the affinity between the water molecules from the coordination sphere and the cation. Indeed, the affinity of the cation for water molecules increases in the reverse order: Ba2+ < Ca2+ < Zn2+ < Mg2+. Finally, we have used the three polysaccharides (PGA, LMP and ALMP - amidated low methoxyl pectin) in association with calcium ions to produce microparticles containing rutin to target drug release in the intestine. We have linked the rutin release kinetics to the network structure established in the gelation step. ALMP microparticles had higher ability to uptake water and thus higher drug release rate than two others microparticles (Ca-LMP and Ca-PGA). The Ca-ALMP gel was more flexible and had the lower viscoelastic modulus than Ca-PGA and Ca-LMP gels. We attributed this to the random distribution of ester and/or amide groups in ALMP, which hinders the formation of dimers: the hydrogen bonds between the amine groups and carboxylate groups are responsible for the flexibility of the network formed.

https://theses.hal.science/tel-01508191