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dc.contributor.authorHossieni-Aghdam, SJ
dc.contributor.authorForoughi-Nia, B
dc.contributor.authorZare-Akbari, Z
dc.contributor.authorMojarad-Jabali, S
dc.contributor.authorMotasadizadeh, H
dc.contributor.authorFarhadnejad, H
dc.date.accessioned2018-08-26T04:55:48Z
dc.date.available2018-08-26T04:55:48Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38405
dc.description.abstractThe main aim of the present study was to design pH-sensitive bionanocomposite hydrogel beads based on CMC and HNT-AT nanohybrid and evaluate whether prepared bionanocomposite beads have the potential to be used in drug delivery applications. Atenolol (AT), as a model drug, was incorporated into the lumen of HA nanotubes via the co-precipitation technique. HNT/AT nanohybrid and CMC/HNT-AT beads were characterized via XRD, SEM, TGA, and FT-IR techniques. Drug loading and encapsulation efficiency was found to be high for CMC/HNT3 beads. Moreover, the swelling and drug release properties of the prepared CMC/HA-AT beads were investigated, and showed a pH sensitive swelling behavior with maximum its content at pH 6.8. Also, it was found that the swelling ratio of CMC/HNT beads was lower than that of pristine CMC beads. Drug release behavior of CMC/HNT-AT bionanocomposite hydrogel beads were investigated. A more sustained and controlled drug releases were observed for CMC/HNT-AT beads.
dc.language.isoEnglish
dc.relation.ispartofInternational journal of biological macromolecules
dc.subjectAluminum Silicates
dc.subjectAtenolol
dc.subjectCarboxymethylcellulose Sodium
dc.subjectDrug Delivery Systems
dc.subjectDrug Liberation
dc.subjectHumans
dc.subjectHydrogel, Polyethylene Glycol Dimethacrylate
dc.subjectHydrogen-Ion Concentration
dc.subjectNanocomposites
dc.titleFacile fabrication and characterization of a novel oral pH-sensitive drug delivery system based on CMC hydrogel and HNT-AT nanohybrid.
dc.typearticle
dc.citation.volume107
dc.citation.issuePt B
dc.citation.spage2436
dc.citation.epage2449
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.ijbiomac.2017.10.128


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