Publication:
Controllable encapsulation of α-mangostin with quaternized β-cyclodextrin grafted chitosan using high shear mixing

dc.contributor.authorSarunya Phunpeeen_US
dc.contributor.authorKunat Sukthamen_US
dc.contributor.authorSuvimol Surassmoen_US
dc.contributor.authorSuwatchai Jarussophonen_US
dc.contributor.authorChompoonut Rungnimen_US
dc.contributor.authorApinan Soottitantawaten_US
dc.contributor.authorSatit Puttipipatkhachornen_US
dc.contributor.authorUracha Rungsardthong Ruktanonchaien_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.date.accessioned2019-08-28T06:53:00Z
dc.date.available2019-08-28T06:53:00Z
dc.date.issued2018-03-01en_US
dc.description.abstract© 2017 Elsevier B.V. In this study, the inclusion complex formation between α-mangostin and water-soluble quaternized β-CD grafted-chitosan (QCD-g-CS) was investigated. Inclusion complex formation with encapsulation efficiency (%EE) of 5, 15 and 75% can be varied using high speed homogenizer. Tuning %EE plays a role on physicochemical and biological properties of α-mangostin/QCD-g-CS complex. Molecular dynamics simulations indicate that α-mangostin is included within the hydrophobic β-CD cavity and being absorbed on the QCD-g-CS surface, with these results being confirmed by Fourier transform infrared (FTIR) spectroscopy. Probing the release characteristics of the inclusion complex at various %EE (5%, 15% and 75%) in simulated saliva (pH 6.8) demonstrated that α-mangostin release rates were dependent on % EE (order 5% > 15% > 75%). Additionally, higher antimicrobial and anti-inflammation activities were observed for the inclusion complex than those of free α-mangostin due to enhance the solubility of α-mangostin through the inclusion complex with QCD-g-CS.en_US
dc.identifier.citationInternational Journal of Pharmaceutics. Vol.538, No.1-2 (2018), 21-29en_US
dc.identifier.doi10.1016/j.ijpharm.2017.12.016en_US
dc.identifier.issn18733476en_US
dc.identifier.issn03785173en_US
dc.identifier.other2-s2.0-85040354898en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/47324
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85040354898&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleControllable encapsulation of α-mangostin with quaternized β-cyclodextrin grafted chitosan using high shear mixingen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85040354898&origin=inwarden_US

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