Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117637
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dc.contributorDepartment of Biomedical Engineering-
dc.creatorCheung, HPH-
dc.creatorLauwers, M-
dc.creatorWang, Z-
dc.creatorWang, J-
dc.creatorNing, C-
dc.creatorKer, DFE-
dc.creatorWang, DM-
dc.date.accessioned2026-02-26T03:47:38Z-
dc.date.available2026-02-26T03:47:38Z-
dc.identifier.urihttp://hdl.handle.net/10397/117637-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rights© The Author(s) 2025en_US
dc.rightsThe following publication Cheung, H., Lauwers, M., Wang, Z. et al. Rapid sonication-assisted whole tissue clearing and immunostaining. Sci Rep 15, 35101 (2025) is available at https://doi.org/10.1038/s41598-025-18928-5.en_US
dc.subjectOptical imagingen_US
dc.subjectSonicationen_US
dc.subjectTissue clearingen_US
dc.subjectWhole-tissue immunostainingen_US
dc.titleRapid sonication-assisted whole tissue clearing and immunostainingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume15-
dc.identifier.doi10.1038/s41598-025-18928-5-
dcterms.abstractHigh-resolution mapping of three-dimensional structures in biological tissues is essential for understanding various biological processes. However, the optical heterogeneity of these tissues, marked by varying optical properties, causes light scattering and absorption, complicating imaging. Current tissue clearing methods can take between 48 h and 32 days, and the limited diffusion depth of fluorescent probes restricts whole-tissue imaging. This study introduces an innovative Sonication-Assisted Tissue Clearing and Immunofluorescent Staining method (SoniC/S), which combines low-frequency ultrasound with a commercial chemical clearing kit and iDISCO staining techniques. When tested on the soft tissue of mouse muscle, the dense collagenous tissue of rat tendon, and the heme-rich tissue of mouse spleen, SoniC/S achieved complete clearing in just 36 h and uniform labeling in 15 h. Overall, SoniC/S provides a rapid and effective approach for tissue clearing and deep immunostaining, facilitating high-resolution volumetric imaging in biological research.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationScientific reports, 2025, v. 15, 35101-
dcterms.isPartOfScientific reports-
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105018282707-
dc.identifier.pmid41062556-
dc.identifier.eissn2045-2322-
dc.identifier.artn35101-
dc.description.validate202602 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the Research Grants Council of Hong Kong SAR (GRF 14118620 and 14121121, D.M.W.), The National Natural Science Foundation of China/Research Grants Council Joint Research Scheme (N_CUHK409/23, D.M.W.), and the Innovation and Technology Commission of the Hong Kong SAR Government (ITS-020-23MX, D.M.W.). This study was funded in part by the InnoHK initiative of the Innovation and Technology Commission of the Hong Kong Special Administrative Region Government (D.F.E.K., and D.M.W.).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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