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dc.contributor.authorWasu Witoonsaridsilpen_US
dc.contributor.authorOrnlaksana Paeratakulen_US
dc.contributor.authorBusaba Panyarachunen_US
dc.contributor.authorNarong Sarisutaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.date.accessioned2018-06-11T05:23:26Z-
dc.date.available2018-06-11T05:23:26Z-
dc.date.issued2012-06-01en_US
dc.identifier.citationAAPS PharmSciTech. Vol.13, No.2 (2012), 699-706en_US
dc.identifier.issn15309932en_US
dc.identifier.other2-s2.0-84862904378en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862904378&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/15164-
dc.description.abstractThe lysozyme (LZ)-entrapped mannosylated liposomes were prepared in this study by the use of N-octadecyl-d-mannopyranosylamine (SAMAN), which had been synthesized in-house and confirmed by characterization with FTIR and NMR. The reactant residues of synthesized SAMAN were found to be less than 1%. The mean sizes, zeta potentials, drug entrapment efficiencies, and loading capacities of all liposomal formulations were in the ranges of 234.7 to 431.0 nm, -10.97 to -25.80 mV, 7.52 to 14.10%, and 1.44 to 2.77%, respectively. The permeability of mannosylated LZ liposomes across Caco-2 cell monolayers was significantly enhanced to about 2.5- and 7-folds over those of conventional liposomes and solution, respectively, which might be due to the role of mannose receptor or mannose-binding protein on the intestinal enterocytes. © 2012 American Association of Pharmaceutical Scientists.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862904378&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleDevelopment of mannosylated liposomes using synthesized N-octadecyl-D-mannopyranosylamine to enhance gastrointestinal permeability for protein deliveryen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1208/s12249-012-9788-1en_US
Appears in Collections:Scopus 2011-2015

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