Multilamellar ceramide core-structured microvehicles with substantial skin barrier function recovery

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dc.contributor.authorShin, Kyoungheeko
dc.contributor.authorLee, Kun Bongko
dc.contributor.authorHwang, Jee-Hyunko
dc.contributor.authorLee, Boryeongko
dc.contributor.authorRyu, Hyunsunko
dc.contributor.authorNoh, Minjooko
dc.contributor.authorLee, Jun Baeko
dc.contributor.authorNam, Yoon Sungko
dc.contributor.authorLim, Kyung-Minko
dc.contributor.authorKim, Jin Woongko
dc.date.accessioned2023-03-22T06:01:15Z-
dc.date.available2023-03-22T06:01:15Z-
dc.date.created2023-03-13-
dc.date.issued2023-03-
dc.identifier.citationJOURNAL OF MATERIALS CHEMISTRY B, v.11, no.10, pp.2135 - 2144-
dc.identifier.issn2050-7518-
dc.identifier.urihttp://hdl.handle.net/10203/305726-
dc.description.abstractThis study introduces a multilamellar ceramide core-structured microvehicle platform for substantial skin barrier function recovery. Our approach essentially focused on fabricating bacterial cellulose nanofiber (BCNF)-enveloped ceramide-rich lipid microparticles (CerMPs) by solidifying BCNF-armored oil-in-water Pickering emulsions. The oil drops consisted of Ceramide NP (a phytosphingosine backbone N-acylated with a saturated stearic acid) and fatty alcohols (FAs) with a designated stoichiometry. The thin BCNF shell layer completely blocked the growth of ceramide molecular crystals from the CerMPs for a long time. The CerMP cores displayed a multilamellar structure wherein the interlayer distance and lateral packing could be manipulated using FAs with different alkyl chain lengths. The CerMPs remarkably lowered the trans-epidermal water loss while restoring the structural integrity of the epidermis in damaged skin. The results obtained herein highlight that the CerMP system provides a practical methodology for developing various types of skin-friendly formulations that can strengthen the skin barrier function.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleMultilamellar ceramide core-structured microvehicles with substantial skin barrier function recovery-
dc.typeArticle-
dc.identifier.wosid000933157800001-
dc.identifier.scopusid2-s2.0-85148675171-
dc.type.rimsART-
dc.citation.volume11-
dc.citation.issue10-
dc.citation.beginningpage2135-
dc.citation.endingpage2144-
dc.citation.publicationnameJOURNAL OF MATERIALS CHEMISTRY B-
dc.identifier.doi10.1039/d2tb02734h-
dc.contributor.localauthorNam, Yoon Sung-
dc.contributor.nonIdAuthorShin, Kyounghee-
dc.contributor.nonIdAuthorLee, Kun Bong-
dc.contributor.nonIdAuthorHwang, Jee-Hyun-
dc.contributor.nonIdAuthorLee, Boryeong-
dc.contributor.nonIdAuthorRyu, Hyunsun-
dc.contributor.nonIdAuthorNoh, Minjoo-
dc.contributor.nonIdAuthorLee, Jun Bae-
dc.contributor.nonIdAuthorLim, Kyung-Min-
dc.contributor.nonIdAuthorKim, Jin Woong-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusNANOEMULSION-
dc.subject.keywordPlusFORMULATION-
dc.subject.keywordPlusVESICLES-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusPHASE-
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