Publication:
A comparison of eugenol and menthol on encapsulation characteristics with water-soluble quaternized β-cyclodextrin grafted chitosan

dc.contributor.authorSarunya Phunpeeen_US
dc.contributor.authorSomsak Saesooen_US
dc.contributor.authorIssara Sramalaen_US
dc.contributor.authorSuwatchai Jarussophonen_US
dc.contributor.authorWarayuth Sajomsangen_US
dc.contributor.authorSatit Puttipipatkhajornen_US
dc.contributor.authorApinan Soottitantawaten_US
dc.contributor.authorUracha Rungsardthong Ruktanonchaien_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.date.accessioned2018-12-11T02:18:32Z
dc.date.accessioned2019-03-14T08:04:05Z
dc.date.available2018-12-11T02:18:32Z
dc.date.available2019-03-14T08:04:05Z
dc.date.issued2016-03-01en_US
dc.description.abstract© 2015 Elsevier B.V. Two guest molecules (eugenol and (-)-menthol) were investigated on inclusion complex formation with water-soluble quaternized β-CD grafted with chitosan (QCD-g-CS). The inclusion complexes were prepared at varying mole ratios between eugenol or (-)-menthol and β-CD (substituted on QCD-g-CS) by a conventional shaking method and obtained as solid powder by freeze-drying process. The results showed that encapsulation efficiency %EE decreased with increasing of initial eugenol or (-)-menthol loading whereas %loading increased with increasing of initial eugenol or (-)-menthol loading. The results indicated that inclusion complex formation between eugenol and QCD-g-CS was more favorable than that of (-)-menthol. To clarify this mechanism, molecular dynamics simulations were performed to explore their binding energy, solvation energy and total free energy of those complexes. It was found that the total free energy (ΔG) of eugenol and (-)-menthol against QCD-g-CS (mole ratio of 1) in water-explicit system were -2108.91 kJ/mol and -344.45 kJ/mol, respectively. Moreover, molecular dynamic simulation of eugenol absorbed on surface QCD-g-CS (-205.73 kJ/mol) was shown to have a higher negative value than that of (-)-menthol on QCD-gCS (3182.31 kJ/mol). Furthermore, the release characteristics of the encapsulated powder were also investigated in simulated saliva pH 6.8 at 32 °C. The results suggested that (-)-menthol had higher release rate from the complexes than eugenol. In all cases, the release characteristics for those guest molecules could be characterized by the limited-diffusion kinetics.en_US
dc.identifier.citationInternational Journal of Biological Macromolecules. Vol.84, (2016), 472-480en_US
dc.identifier.doi10.1016/j.ijbiomac.2015.11.006en_US
dc.identifier.issn18790003en_US
dc.identifier.issn01418130en_US
dc.identifier.other2-s2.0-84956582512en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43029
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84956582512&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleA comparison of eugenol and menthol on encapsulation characteristics with water-soluble quaternized β-cyclodextrin grafted chitosanen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84956582512&origin=inwarden_US

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