Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13912
Title: Combating Helicobacter pylori infections with mucoadhesive nanoparticles loaded with Garcinia mangostana extract
Authors: Pan-In P.
Tachapruetinun A.
Chaichanawongsaroj N.
Banlunara W.
Suksamrarn S.
Wanichwecharungruang S.
Keywords: alpha mangostin
amoxicillin
antiinfective agent
clarithromycin
Garcinia mangostana extract
metronidazole
nanocarrier
plant extract
unclassified drug
adhesin
drug carrier
mangostin
nanoparticle
plant extract
xanthone derivative
acidity
animal cell
animal experiment
animal model
animal tissue
antiadhesion activity
antibacterial activity
article
bacterial strain
bacterium detection
column chromatography
controlled study
differential scanning calorimetry
drug activity
drug delivery system
drug isolation
drug stability
Garcinia mangostana
Helicobacter infection
Helicobacter pylori
high performance liquid chromatography
human
human cell
in vitro study
in vivo study
minimum inhibitory concentration
mouse
mucoadhesion
nanoencapsulation
nonhuman
priority journal
scanning electron microscope
scanning electron microscopy
spectrophotometer
stomach mucosa
sustained drug release
animal
C57BL mouse
cell line
chemistry
drug effects
Garcinia mangostana
Helicobacter Infections
microbiology
physiology
stomach
Adhesins, Bacterial
Animals
Cell Line
Drug Carriers
Garcinia mangostana
Helicobacter Infections
Helicobacter pylori
Humans
Mice
Mice, Inbred C57BL
Nanoparticles
Plant Extracts
Stomach
Xanthones
Issue Date: 2014
Abstract: Aim: 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.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13912
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84898936119&doi=10.2217%2fnnm.13.30&partnerID=40&md5=0bdd3bda21deea7f14f0491906eb356a
ISSN: 17435889
Appears in Collections:Scopus 1983-2021

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