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DC Field | Value | Language |
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dc.contributor.author | Juvekar, Vinayak | - |
dc.contributor.author | Lee, Hyo Won | - |
dc.contributor.author | Lee, Dong Joon | - |
dc.contributor.author | Kim, Hwan Myung | - |
dc.date.issued | 2022-12-01 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/dev/handle/2018.oak/32982 | - |
dc.description.abstract | Two-photon (TP) microscopy (TPM) is an indispensable visualization tool for deep-tissue imaging. TPM uses the low energy light of the near-infrared window as an excitation source of fluorophores which reduces autofluorescence, photodamage, and light scattering, resulting in high resolution fluorescence images potentially beyond several millimeter depths in living systems. Due to the continuous development of the microscope and advances in optical output algorithms, it is crucial to develop innovative strategies for the quantitative analysis of biomedically relevant target analytes in living systems using TP fluorescence probes. In this review, we have highlighted ratiometric TP probe design strategies with representative ratiometric TP sensors in the last decade. We have also summarized the recent progress in the development of TP probes published between 2017 and 2022 for quantitatively detecting analytes such as enzymes, reactive species, bio-thiols, pH, neutral molecules, and metal ions in live cells and tissues. | - |
dc.description.sponsorship | This work was supported by grants from the National Leading Research Lab Program of the National Research Foundation of Korea (NRF) , funded by the Korean government ( MSIP ) ( NRF-2022R1A2B5B03001607 ), Center for Convergence Research of Neurological Disorders ( NRF-2019R1A5A2026045 ), Basic Science Research Program ( NRF-2021R1A6A1A10044950 ), and the Ajou University Research Fund . | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.subject.mesh | Bio-imaging | - |
dc.subject.mesh | Fluorescent probes | - |
dc.subject.mesh | Imaging analysis | - |
dc.subject.mesh | Live tissue | - |
dc.subject.mesh | Living systems | - |
dc.subject.mesh | Ratiometric | - |
dc.subject.mesh | Tissue imaging | - |
dc.subject.mesh | Two photon | - |
dc.subject.mesh | Two photon microscopy | - |
dc.subject.mesh | Two-photon probes | - |
dc.title | Two-photon fluorescent probes for quantitative bio-imaging analysis in live tissues | - |
dc.type | Review | - |
dc.citation.title | TrAC - Trends in Analytical Chemistry | - |
dc.citation.volume | 157 | - |
dc.identifier.bibliographicCitation | TrAC - Trends in Analytical Chemistry, Vol.157 | - |
dc.identifier.doi | 10.1016/j.trac.2022.116787 | - |
dc.identifier.scopusid | 2-s2.0-85139592986 | - |
dc.identifier.url | www.elsevier.com/locate/trac | - |
dc.subject.keyword | Bio-imaging | - |
dc.subject.keyword | Quantitative analysis | - |
dc.subject.keyword | Tissue imaging | - |
dc.subject.keyword | Two-photon microscopy | - |
dc.subject.keyword | Two-photon probes | - |
dc.description.isoa | false | - |
dc.subject.subarea | Analytical Chemistry | - |
dc.subject.subarea | Spectroscopy | - |
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