Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13912
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dc.contributor.authorPan-In P.
dc.contributor.authorTachapruetinun A.
dc.contributor.authorChaichanawongsaroj N.
dc.contributor.authorBanlunara W.
dc.contributor.authorSuksamrarn S.
dc.contributor.authorWanichwecharungruang S.
dc.date.accessioned2021-04-05T03:32:39Z-
dc.date.available2021-04-05T03:32:39Z-
dc.date.issued2014
dc.identifier.issn17435889
dc.identifier.other2-s2.0-84898936119
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13912-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84898936119&doi=10.2217%2fnnm.13.30&partnerID=40&md5=0bdd3bda21deea7f14f0491906eb356a
dc.description.abstractAim: To combat the resistance of Helicobacter pylori to antibiotics through the use of Garcinia mangostana extract (GME) in the form that can be localized at stomach mucosa. Materials & methods: GME and its major active component, α-mangostin, are encapsulated into the moderately acid stable mucoadhesive nanocarriers, and tested for anti-H. pylori and antiadhesion activities in vitro and their ability to eradicate H. pylori in infected mice. Results: The two in vitro activities are observed and are enhanced when the materials are encapsulated into nanocarriers. Preliminary in vivo tests revealed the ability to combat H. pylori in mice following oral administration of the encapsulated GME, but not the unencapsulated GME. Conclusion: Nanoencapsulated GME is a potential anti-H. pylori agent. Original submitted 10 August 2012; Revised submitted 9 December 2012; Published online 3 June 201. © 2014 Future Medicine Ltd.
dc.subjectalpha mangostin
dc.subjectamoxicillin
dc.subjectantiinfective agent
dc.subjectclarithromycin
dc.subjectGarcinia mangostana extract
dc.subjectmetronidazole
dc.subjectnanocarrier
dc.subjectplant extract
dc.subjectunclassified drug
dc.subjectadhesin
dc.subjectdrug carrier
dc.subjectmangostin
dc.subjectnanoparticle
dc.subjectplant extract
dc.subjectxanthone derivative
dc.subjectacidity
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantiadhesion activity
dc.subjectantibacterial activity
dc.subjectarticle
dc.subjectbacterial strain
dc.subjectbacterium detection
dc.subjectcolumn chromatography
dc.subjectcontrolled study
dc.subjectdifferential scanning calorimetry
dc.subjectdrug activity
dc.subjectdrug delivery system
dc.subjectdrug isolation
dc.subjectdrug stability
dc.subjectGarcinia mangostana
dc.subjectHelicobacter infection
dc.subjectHelicobacter pylori
dc.subjecthigh performance liquid chromatography
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectin vivo study
dc.subjectminimum inhibitory concentration
dc.subjectmouse
dc.subjectmucoadhesion
dc.subjectnanoencapsulation
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectscanning electron microscope
dc.subjectscanning electron microscopy
dc.subjectspectrophotometer
dc.subjectstomach mucosa
dc.subjectsustained drug release
dc.subjectanimal
dc.subjectC57BL mouse
dc.subjectcell line
dc.subjectchemistry
dc.subjectdrug effects
dc.subjectGarcinia mangostana
dc.subjectHelicobacter Infections
dc.subjectmicrobiology
dc.subjectphysiology
dc.subjectstomach
dc.subjectAdhesins, Bacterial
dc.subjectAnimals
dc.subjectCell Line
dc.subjectDrug Carriers
dc.subjectGarcinia mangostana
dc.subjectHelicobacter Infections
dc.subjectHelicobacter pylori
dc.subjectHumans
dc.subjectMice
dc.subjectMice, Inbred C57BL
dc.subjectNanoparticles
dc.subjectPlant Extracts
dc.subjectStomach
dc.subjectXanthones
dc.titleCombating Helicobacter pylori infections with mucoadhesive nanoparticles loaded with Garcinia mangostana extract
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationNanomedicine. Vol 9, No.3 (2014), p.457-468
dc.identifier.doi10.2217/nnm.13.30
Appears in Collections:Scopus 1983-2021

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