2022
DOI: 10.1038/s41592-022-01394-6
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Targeted multicolor in vivo imaging over 1,000 nm enabled by nonamethine cyanines

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Cited by 91 publications
(97 citation statements)
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“…In FRET and secondary absorption systems, molecular dyes absorb and quench the emission light of inorganic emitters to quench the fluorescence signal or influence luminescence lifetime (MY-1057, 49 Flav7, 53 5H5, 54 CX-3, 55 BTC1070, 56 Rh-1029, 57 VIX-4, 58 NIRII-HD5, 59 LET-1052, 51 NRh, 42 NIR-1380, 60 and FNIR-1072. 61 ). However, in dye sensitizing and ACIE systems, molecular dyes absorb excitation light, and then either transfer energy to emitters (in a dye sensitizing system, such as ICG, 62 ALK-pi, 63 and NPh 64 ) or quench the emitters (in ACIE systems, such as IR-808, 65 and NPTAT 66 ).…”
Section: Construction Of Nir-ii Organic/inorganic Nanohybridsmentioning
confidence: 99%
“…In FRET and secondary absorption systems, molecular dyes absorb and quench the emission light of inorganic emitters to quench the fluorescence signal or influence luminescence lifetime (MY-1057, 49 Flav7, 53 5H5, 54 CX-3, 55 BTC1070, 56 Rh-1029, 57 VIX-4, 58 NIRII-HD5, 59 LET-1052, 51 NRh, 42 NIR-1380, 60 and FNIR-1072. 61 ). However, in dye sensitizing and ACIE systems, molecular dyes absorb excitation light, and then either transfer energy to emitters (in a dye sensitizing system, such as ICG, 62 ALK-pi, 63 and NPh 64 ) or quench the emitters (in ACIE systems, such as IR-808, 65 and NPTAT 66 ).…”
Section: Construction Of Nir-ii Organic/inorganic Nanohybridsmentioning
confidence: 99%
“…We recently demonstrated that dichloro-substituted nonamethine cyanine derivatives could be modified with either catechols or through direct aryl fusion to generate FNIR-866 and FNIR-1072, respectively ( Figure 3 b). These probes can be used as mAb-targeted agents for multicolor surgical applications [ 142 ]. Overall, the rapid progress in the field of long-wavelength probe chemistry is opening up a range of exciting possibilities.…”
Section: Recent Developments In Nir and Swir Fluorophoresmentioning
confidence: 99%
“…The current array of preclinically validated SWIR targeting agents will still require further validation and toxicology studies before reaching clinical deployment. (36,40,42) Clinical SWIR translation has predominantly focused on non-targeted ICG based imaging and has already shown significant improvements over NIR imaging for liver tumor surgery, glioma resection, cystic renal mass removal and brain metastasis. (43)(44)(45)(46) Fortunately, pHLIP ICG (pH low insertion peptide, conjugated to ICG), which until this point has not been validated with SWIR imaging, is a tumor targeting agent that is currently undergoing clinical trials for imaging-guided breast cancer resection (NCT05130801).…”
Section: Introductionmentioning
confidence: 99%
“…( 39 ) In addition to ICG imaging there has been a rapid development of dedicated SWIR fluorescence agents for in vivo applications. ( 40, 41 ) One area which would greatly benefit from SWIR imaging is that of clinical cancer resection. In comparison to functional imaging of e.g., calcium dynamics, cancer resection provides a more facile translation for SWIR imaging where imaging can be performed with a binary output of tumor/no tumor for resection if a dye can be targeted and localized to a tumor.…”
Section: Introductionmentioning
confidence: 99%
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