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Article: Biological imaging without autofluorescence in the second near-infrared region

TitleBiological imaging without autofluorescence in the second near-infrared region
Authors
Keywordsautofluorescence
fluorescence imaging
nanotechnology
second near-infrared
Issue Date2015
Citation
Nano Research, 2015, v. 8, n. 9, p. 3027-3034 How to Cite?
AbstractFluorescence imaging is capable of acquiring anatomical and functional information with high spatial and temporal resolution. This imaging technique has been indispensable in biological research and disease detection/diagnosis. Imaging in the visible and to a lesser degree, in the near-infrared (NIR) regions below 900 nm, suffers from autofluorescence arising from endogenous fluorescent molecules in biological tissues. This autofluorescence interferes with fluorescent molecules of interest, causing a high background and low detection sensitivity. Here, we report that fluorescence imaging in the 1,500–1,700-nm region (termed “NIR-IIb”) under 808-nm excitation results in nearly zero tissue autofluorescence, allowing for background-free imaging of fluorescent species in otherwise notoriously autofluorescent biological tissues, including liver. Imaging of the intrinsic fluorescence of individual fluorophores, such as a single carbon nanotube, can be readily achieved with high sensitivity and without autofluorescence background in mouse liver within the 1,500–1,700-nm wavelength region. [Figure not available: see fulltext.]
Persistent Identifierhttp://hdl.handle.net/10722/334401
ISSN
2023 Impact Factor: 9.5
2023 SCImago Journal Rankings: 2.539
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDiao, Shuo-
dc.contributor.authorHong, Guosong-
dc.contributor.authorAntaris, Alexander L.-
dc.contributor.authorBlackburn, Jeffrey L.-
dc.contributor.authorCheng, Kai-
dc.contributor.authorCheng, Zhen-
dc.contributor.authorDai, Hongjie-
dc.date.accessioned2023-10-20T06:47:52Z-
dc.date.available2023-10-20T06:47:52Z-
dc.date.issued2015-
dc.identifier.citationNano Research, 2015, v. 8, n. 9, p. 3027-3034-
dc.identifier.issn1998-0124-
dc.identifier.urihttp://hdl.handle.net/10722/334401-
dc.description.abstractFluorescence imaging is capable of acquiring anatomical and functional information with high spatial and temporal resolution. This imaging technique has been indispensable in biological research and disease detection/diagnosis. Imaging in the visible and to a lesser degree, in the near-infrared (NIR) regions below 900 nm, suffers from autofluorescence arising from endogenous fluorescent molecules in biological tissues. This autofluorescence interferes with fluorescent molecules of interest, causing a high background and low detection sensitivity. Here, we report that fluorescence imaging in the 1,500–1,700-nm region (termed “NIR-IIb”) under 808-nm excitation results in nearly zero tissue autofluorescence, allowing for background-free imaging of fluorescent species in otherwise notoriously autofluorescent biological tissues, including liver. Imaging of the intrinsic fluorescence of individual fluorophores, such as a single carbon nanotube, can be readily achieved with high sensitivity and without autofluorescence background in mouse liver within the 1,500–1,700-nm wavelength region. [Figure not available: see fulltext.]-
dc.languageeng-
dc.relation.ispartofNano Research-
dc.subjectautofluorescence-
dc.subjectfluorescence imaging-
dc.subjectnanotechnology-
dc.subjectsecond near-infrared-
dc.titleBiological imaging without autofluorescence in the second near-infrared region-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s12274-015-0808-9-
dc.identifier.scopuseid_2-s2.0-84941740985-
dc.identifier.volume8-
dc.identifier.issue9-
dc.identifier.spage3027-
dc.identifier.epage3034-
dc.identifier.eissn1998-0000-
dc.identifier.isiWOS:000361057000025-

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