Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115606
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dc.contributorDepartment of Applied Physics-
dc.contributorResearch Centre for Nanoscience and Nanotechnology-
dc.creatorLao, X-
dc.creatorBai, Q-
dc.creatorZhao, Y-
dc.creatorDai, X-
dc.creatorLiu, Y-
dc.creatorHan, X-
dc.creatorHao, J-
dc.date.accessioned2025-10-08T01:16:59Z-
dc.date.available2025-10-08T01:16:59Z-
dc.identifier.issn1616-301X-
dc.identifier.urihttp://hdl.handle.net/10397/115606-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2025 The Author(s). Advanced Functional Materials published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.en_US
dc.rightsThe following publication X. Lao, Q. Bai, Y. Zhao, X. Dai, Y. Liu, X. Han, J. Hao, Enhanced Sonodynamic Bacterial Elimination and Wound Healing Therapy Based on Lanthanide Ion Doped Bi2WO6 Nanosheets and Hydrogel Platform. Adv. Funct. Mater. 2025, 2511512 is available at https://doi.org/10.1002/adfm.202511512.en_US
dc.subjectAntibacterialen_US
dc.subjectBi2WO6 nanosheetsen_US
dc.subjectSonodynamic therapyen_US
dc.subjectWound healingen_US
dc.titleEnhanced sonodynamic bacterial elimination and wound healing therapy based on lanthanide ion doped Bi₂WO₆ nanosheets and hydrogel platformen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1002/adfm.202511512-
dcterms.abstractSonodynamic therapy (SDT) offers tremendous potential in preventing multidrug-resistant bacterial infections, as it is noninvasive and requires no antibiotic dependence, effectively addressing the issue of bacterial resistance. This study implements an ultrasound (US) responsive 2D Bi2WO6 nanosheets (BWO NSs) as sonosensitizers to generate reactive oxygen species (ROS), resulting in sonodynamic broad-spectrum bacterial elimination. Notably, lanthanide Ytterbium ions are introduced (BWO-x%Yb NSs) to boost the generation of ROS, leading to an enhanced antibacterial effect. The RNA sequencing further reveals the underlying antibacterial mechanism, wherein ROS induces lipid oxidation in bacterial cell membranes and deterioration of membrane integrity, ultimately leading to cellular death. In vitro experiments verify that BWO-x%Yb NSs sonosensitizers attain 100% elimination on Methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli) under US irradiation, demonstrating a broad-spectrum bactericidal ability. Furthermore, to improve the biocompatibility for in vivo SDT, BWO-x%Yb NSs are integrated with hydrogel, serving as a sonosensitizer-hydrogel platform. This platform expedites the healing process of MRSA-infected wounds under ultrasonic stimulation and reduces the wound area by 75% in 10 Days. Therefore, this work highlights the potential of 2D BWO NSs as US-responsive sonosensitizers and a prospective biocompatible sonosensitizer-hydrogel platform for in vivo SDT applications.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced functional materials, First published: 11 June 2025, Early View, 2511512, https://doi.org/10.1002/adfm.202511512-
dcterms.isPartOfAdvanced functional materials-
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105007883110-
dc.identifier.eissn1616-3028-
dc.identifier.artn2511512-
dc.description.validate202510 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TAen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by grants from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. CRF No. C5110-20G and PolyU SRFS2122-5S02), and PolyU Grants (1-CE0H, 1-W30M, 1-W327, and 1-CD7V).en_US
dc.description.pubStatusEarly releaseen_US
dc.description.TAWiley (2025)en_US
dc.description.oaCategoryTAen_US
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