Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/94422
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.contributorMainland Development Officeen_US
dc.creatorYao, Jen_US
dc.creatorGao, Yen_US
dc.creatorYin, Yen_US
dc.creatorLai, Pen_US
dc.creatorYe, Sen_US
dc.creatorZheng, Wen_US
dc.date.accessioned2022-08-16T07:41:23Z-
dc.date.available2022-08-16T07:41:23Z-
dc.identifier.issn0146-9592en_US
dc.identifier.urihttp://hdl.handle.net/10397/94422-
dc.language.isoenen_US
dc.publisherOptical Society of Americaen_US
dc.rights© 2022 Optica Publishing Groupen_US
dc.rights© 2022 Optical Society of America. One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modifications of the content of this paper are prohibited.en_US
dc.rightsThe following publication Jing Yao, Yufeng Gao, Yixuan Yin, Puxiang Lai, Shiwei Ye, and Wei Zheng, "Exploiting the potential of commercial objectives to extend the field of view of two-photon microscopy by adaptive optics," Opt. Lett. 47, 989-992 (2022) is available at https://dx.doi.org/10.1364/OL.450973.en_US
dc.titleExploiting the potential of commercial objectives to extend the field of view of two-photon microscopy by adaptive opticsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage989en_US
dc.identifier.epage992en_US
dc.identifier.volume47en_US
dc.identifier.issue4en_US
dc.identifier.doi10.1364/OL.450973en_US
dcterms.abstractTwo-photon microscopy (TPM) has provided critical in situ and in vivo information in biomedical studies due to its high resolution, intrinsic optical sectioning, and deep penetration. However, its relatively small field of view (FOV), which is usually determined by objectives, restricts its wide application. In this paper, we propose a segment-scanning sensorless adaptive optics method to extend the FOV and achieve high-resolution and large-FOV two-photon imaging. We demonstrated the proposed method by imaging fluorescent beads, cerebral nerve cells of mouse brain slices, and cerebral vasculature and microglia of live mice. The method extended the FOV of a commercial objective from 1.8 to 3.46 mm while maintaining a lateral resolution of 840 nm and high signal-to-noise ratio. Our technology is compatible with a standard TPM and can be used for large-scale biological exploration.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOptics letters, 15 Feb. 2022, v. 47, no. 4, p. 989-992en_US
dcterms.isPartOfOptics lettersen_US
dcterms.issued2022-02-15-
dc.identifier.isiWOS:000756709400065-
dc.identifier.scopus2-s2.0-85124679744-
dc.identifier.pmid35167576-
dc.identifier.eissn1539-4794en_US
dc.description.validate202208 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera1563-
dc.identifier.SubFormID45434-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
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