Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/146651
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dc.contributor.authorLiu, Yu-Chien_US
dc.contributor.authorKe, Linen_US
dc.contributor.authorYang, Steve Wu Qingen_US
dc.contributor.authorNan, Zhangen_US
dc.contributor.authorTeo, Ericia Pei Wenen_US
dc.contributor.authorLwin, Nyein Chanen_US
dc.contributor.authorLin, Molly Tzu-Yuen_US
dc.contributor.authorLee, Isabelle Xin Yuen_US
dc.contributor.authorChan, Anita Sook-Yeeen_US
dc.contributor.authorSchmetterer, Leopolden_US
dc.contributor.authorMehta, Jodhbir Singhen_US
dc.date.accessioned2021-03-04T05:49:08Z-
dc.date.available2021-03-04T05:49:08Z-
dc.date.issued2021-
dc.identifier.citationLiu, Y.-C., Ke, L., Yang, S. W. Q., Nan, Z., Teo, E. P. W., Lwin, N. C., . . . Mehta, J. S. (2021). Safety profiles of terahertz scanning in ophthalmology. Scientific Reports, 11(1), 2448-. doi:10.1038/s41598-021-82103-9en_US
dc.identifier.issn2045-2322en_US
dc.identifier.urihttps://hdl.handle.net/10356/146651-
dc.description.abstractTerahertz (THz) technology has emerged recently as a potential novel imaging modality in biomedical fields, including ophthalmology. However, the ocular biological responses after THz electromagnetic exposure have not been investigated. We conducted a rabbit study to evaluate the safety profiles of THz scanning on eyes, at a tissue, cellular, structural and functional level. Eight animals (16 eyes) were analysed after excessive THz exposure (control, 1 h, 4 h, and 1 week after continuous 4-h exposure; THz frequency = 0.3 THz with continuous pulse generated at 40 µW). We found that at all the time points, the corneas and lens remained clear with no corneal haze or lens opacity formation clinically and histopathologically. No thermal effect, assessed by thermographer, was observed. The rod and cone cell-mediated electroretinography responses were not significantly altered, and the corneal keratocytes activity as well as endothelial viability, assessed by in-vivo confocal microscopy, was not affected. Post-exposed corneas, lens and retinas exhibited no significant changes in the mRNA expression of heat shock protein (HSP)90AB1), DNA damage inducible transcript 3 (DDIT3), and early growth response (EGR)1. These tissues were also negative for the inflammatory (CD11b), fibrotic (fibronectin and α-smooth muscle actin), stress (HSP-47) and apoptotic (TUNEL assay) responses on the immunohistochemical analyses. The optical transmittance of corneas did not change significantly, and the inter-fibrillar distances of the corneal stroma evaluated with transmission electron microscopy were not significantly altered after THz exposure. These results provide the basis for future research work on the development of THz imaging system for its application in ophthalmology.en_US
dc.description.sponsorshipNational Medical Research Council (NMRC)en_US
dc.language.isoenen_US
dc.relationR1482/65/2017en_US
dc.relation.ispartofScientific Reportsen_US
dc.rights© 2021 The Author(s). 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.subjectEngineering::Bioengineeringen_US
dc.titleSafety profiles of terahertz scanning in ophthalmologyen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen_US
dc.identifier.doi10.1038/s41598-021-82103-9-
dc.description.versionPublished versionen_US
dc.identifier.pmid33510290-
dc.identifier.scopus2-s2.0-85100021760-
dc.identifier.issue1en_US
dc.identifier.volume11en_US
dc.subject.keywordsMedical Imagingen_US
dc.subject.keywordsTranslational Researchen_US
dc.description.acknowledgementThis research was supported by the Transition Award, National Medical Research Council (R1482/65/2017), Singapore.en_US
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