Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/27481
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dc.contributor.authorSahatsapan N.
dc.contributor.authorPamornpathomkul B.
dc.contributor.authorRojanarata T.
dc.contributor.authorNgawhirunpat T.
dc.contributor.authorPoonkhum R.
dc.contributor.authorOpanasopit P.
dc.contributor.authorPatrojanasophon P.
dc.date.accessioned2022-12-14T03:17:27Z-
dc.date.available2022-12-14T03:17:27Z-
dc.date.issued2022
dc.identifier.issn17732247
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85124595467&doi=10.1016%2fj.jddst.2022.103173&partnerID=40&md5=6767a63b4aa24a4c2732614e309692bd
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/27481-
dc.description.abstractChitosan-maleimide (CSMHA) coated liposomes were developed for the buccal delivery of protein. Albumin–fluorescein isothiocyanate conjugate (FITC-BSA) was used as a protein replica to be loaded in the liposomes. The liposomes were formed by a thin-film hydration technique before being decorated with CSMHA. The mucoadhesive capability of the CSMHA-coated liposomes on the porcine buccal mucosa, the loading efficiency and loading capacity, drug release, permeation through buccal mucosa, protein integrity, the cytotoxicity on oral fibroblast cells, and biocompatibility were investigated. The liposome formulations were obtained with sizes of 35–166 nm. CSMHA-coated FITC-BSA-loaded liposomes remained on the buccal tissue to the highest extent. Moreover, CSMHA-coated liposomes provided the highest buccal permeation of FITC-BSA and were safe for normal gingival fibroblast cells and buccal tissue. Therefore, the CSMHA-coated liposomes may have the capability to improve protein delivery via the buccal route. © 2022 Elsevier B.V.
dc.languageen
dc.titleFeasibility of mucoadhesive chitosan maleimide-coated liposomes for improved buccal delivery of a protein drug
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of Drug Delivery Science and Technology. Vol 69, No. (2022)
dc.identifier.doi10.1016/j.jddst.2022.103173
Appears in Collections:Scopus 2022

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