Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95761
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorBei, HPen_US
dc.creatorXu, Ten_US
dc.creatorZhou, Jen_US
dc.creatorDong, Zen_US
dc.creatorWang, Yen_US
dc.creatorWong, KYen_US
dc.creatorWang, Hen_US
dc.creatorZhao, Xen_US
dc.date.accessioned2022-10-06T06:04:22Z-
dc.date.available2022-10-06T06:04:22Z-
dc.identifier.urihttp://hdl.handle.net/10397/95761-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2022 Elsevier Ltd. All rights reserved.en_US
dc.rights© 2022. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.en_US
dc.rightsThe following publication Bei, H.-P., Xu, T., Zhou, J., Dong, Z., Wang, Y., Wong, K.-Y., Wang, H., & Zhao, X. (2022). Evaporation-based, co-axial lock-and-key fibrous reservoir for long-term prevention of hypertrophic scars. Applied Materials Today, 27, 101463 is available at https://dx.doi.org/10.1016/j.apmt.2022.101463.en_US
dc.subjectDrug deliveryen_US
dc.subjectElectrospinningen_US
dc.subjectGatekeeper nanoparticlesen_US
dc.subjectHypertrophic scarringen_US
dc.subjectLong-term releaseen_US
dc.titleEvaporation-based, co-axial lock-and-key fibrous reservoir for long-term prevention of hypertrophic scarsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume27en_US
dc.identifier.doi10.1016/j.apmt.2022.101463en_US
dcterms.abstractMany diseases and conditions such as hypertrophic scarring require long-term maintenance over the healing cycle to achieve full recovery. However, there is a lack of wound dressings that can sustain over 90 days of therapeutic release. Inspired by the enhancement of wound healing by the nanofibrous morphology and diverse structures of electrospinning, we report an evaporation-based co-axial electrospun fibrous scaffold incorporating polymer brush gatekept nanocarriers for sustained delivery of therapeutics. The release rates of the system were demonstrated to be tunable through polymer graft length, while the system experienced minimal burst release when submerged under aqueous conditions. As a proof-of-concept, we target hypertrophic scarring by loading the system with doxorubicin, which led to inhibition of fibroblast activity without interfering with cell adhesion. Application of our scaffolds on rabbit ear hypertrophic scar models displayed that our scaffolds effectively reduced collagen density and scar-related gene expression in healing tissues, with improved tissue elevation outcomes. We envision that our long-term release scaffolds will be useful in combating long unresolved clinical dilemma such as tendon adhesion and tumor regression.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationApplied materials today, June 2022, v. 27, 101463en_US
dcterms.isPartOfApplied materials todayen_US
dcterms.issued2022-06-
dc.identifier.scopus2-s2.0-85127813543-
dc.identifier.eissn2352-9407en_US
dc.identifier.artn101463en_US
dc.description.validate202210 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera1755-
dc.identifier.SubFormID45891-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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