Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-019-13512-8
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dc.titleSuperhydrophobic hemostatic nanofiber composites for fast clotting and minimal adhesion
dc.contributor.authorLi, Z.
dc.contributor.authorMilionis, A.
dc.contributor.authorZheng, Y.
dc.contributor.authorYee, M.
dc.contributor.authorCodispoti, L.
dc.contributor.authorTan, F.
dc.contributor.authorPoulikakos, D.
dc.contributor.authorYap, C.H.
dc.date.accessioned2021-12-16T07:44:07Z
dc.date.available2021-12-16T07:44:07Z
dc.date.issued2019
dc.identifier.citationLi, Z., Milionis, A., Zheng, Y., Yee, M., Codispoti, L., Tan, F., Poulikakos, D., Yap, C.H. (2019). Superhydrophobic hemostatic nanofiber composites for fast clotting and minimal adhesion. Nature Communications 10 (1) : 5562. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-019-13512-8
dc.identifier.issn20411723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/210688
dc.description.abstractHemostatic materials are of great importance in medicine. However, their successful implementation is still challenging as it depends on two, often counteracting, attributes; achieving blood coagulation rapidly, before significant blood loss, and enabling subsequent facile wound-dressing removal, without clot tears and secondary bleeding. Here we illustrate an approach for achieving hemostasis, rationally targeting both attributes, via a superhydrophobic surface with immobilized carbon nanofibers (CNFs). We find that CNFs promote quick fibrin growth and cause rapid clotting, and due to their superhydrophobic nature they severely limit blood wetting to prevent blood loss and drastically reduce bacteria attachment. Furthermore, minimal contact between the clot and the superhydrophobic CNF surface yields an unforced clot detachment after clot shrinkage. All these important attributes are verified in vitro and in vivo with rat experiments. Our work thereby demonstrates that this strategy for designing hemostatic patch materials has great potential. © 2019, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.1038/s41467-019-13512-8
dc.description.sourcetitleNature Communications
dc.description.volume10
dc.description.issue1
dc.description.page5562
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