2022
DOI: 10.3389/fchem.2022.921354
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Two-Photon Absorption: An Open Door to the NIR-II Biological Window?

Abstract: The way in which photons travel through biological tissues and subsequently become scattered or absorbed is a key limitation for traditional optical medical imaging techniques using visible light. In contrast, near-infrared wavelengths, in particular those above 1000 nm, penetrate deeper in tissues and undergo less scattering and cause less photo-damage, which describes the so-called “second biological transparency window”. Unfortunately, current dyes and imaging probes have severely limited absorption profile… Show more

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Cited by 24 publications
(31 citation statements)
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References 179 publications
(242 reference statements)
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“…Figures 3(a-d) show LSFM images taken at 400, 525, and 650 µm below from the embryo surface facing the detection objective, respectively. However, the imaging resolution is less than the single-photon system since we utilized two-photon excitation 17 .…”
Section: Resultsmentioning
confidence: 99%
“…Figures 3(a-d) show LSFM images taken at 400, 525, and 650 µm below from the embryo surface facing the detection objective, respectively. However, the imaging resolution is less than the single-photon system since we utilized two-photon excitation 17 .…”
Section: Resultsmentioning
confidence: 99%
“…In both experiments we found a measurable increase in the ratio values that is useful in the determination of TYR activity in cells through fluorescence microscopy. Excitation by NIR radiation has been widely used to prevent or reduce autofluorescence of cells and tissues, as well as the absorption and scattering of excitation light, which allows obtaining sharper images at greater depths, although its use is limited in the range of wavelength of higher transmittance in biological samples [6].…”
Section: Discussionmentioning
confidence: 99%
“…autofluorescence, and light scattering. To avoid these drawbacks, a technique can be used that consists in the excitation of the fluorophore by means of two simultaneous photons of a wavelength that doubles or exceeds that needed to excite the same fluorophore with a single photon [4][5][6]. Two-photon microscopy (TPM) was predicted by Nobel laureate Maria Goeppert Mayer in 1931 [7] and was applied by Webb in a cellular environment in 1990 [8].…”
Section: Introductionmentioning
confidence: 99%
“…In addition, this AIETP polymeric nanoparticle demonstrated two-photon NIR-II (1040 nm) excitability, which enables high-contrast vascular brain imaging with increased penetration depth. The NIR-II biological window (1000–1700 nm) is more promising for two-photon bioimaging because tissue components scatter and absorb less at the longer wavelengths, resulting in deeper penetration depth and higher spatial resolution, compared to the visible or conventional NIR-I window [ 31 , 32 ]. However, the design and synthesis of efficient fluorophores are crucial in NIR-II bioimaging.…”
Section: Polymeric Nanoplatforms For Two-photon-assisted Imagingmentioning
confidence: 99%