TY - JOUR
T1 - Multi-Photon Super-Linear Image Scanning Microscopy Using Upconversion Nanoparticles
AU - Wang, Yao
AU - Liu, Baolei
AU - Ding, Lei
AU - Chen, Chaohao
AU - Shan, Xuchen
AU - Wang, Dajing
AU - Tian, Menghan
AU - Song, Jiaqi
AU - Zheng, Ze
AU - Xu, Xiaoxue
AU - Zhong, Xiaolan
AU - Wang, Fan
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/12
Y1 - 2024/12
N2 - Super-resolution fluorescence microscopy is of great interest in life science studies for visualizing subcellular structures at the nanometer scale. Among various kinds of super-resolution approaches, image scanning microscopy (ISM) offers a doubled resolution enhancement in a simple and straightforward manner, based on the commonly used confocal microscopes. ISM is also suitable to be integrated with multi-photon microscopy techniques, such as two-photon excitation and second-harmonic generation imaging, for deep tissue imaging, but it remains the twofold limited resolution enhancement and requires expensive femtosecond lasers. Here, the super-linear ISM (SL-ISM) pushes the resolution enhancement beyond the factor of two is presented and experimentally demonstrated, with a single low-power, continuous-wave, and near-infrared laser, by harnessing the emission nonlinearity within the multiphoton excitation process of lanthanide-doped upconversion nanoparticles (UCNPs). Based on a modified confocal microscope, a resolution of ≈120 nm, 1/8th of the excitation wavelength is achieved. Furthermore, a parallel detection strategy of SL-ISM with the multifocal structured excitation pattern is demonstrated, to speed up the acquisition frame rate. This method suggests a new perspective for super-resolution imaging or sensing, multi-photon imaging, and deep-tissue imaging with simple, low-cost, and straightforward implementations.
AB - Super-resolution fluorescence microscopy is of great interest in life science studies for visualizing subcellular structures at the nanometer scale. Among various kinds of super-resolution approaches, image scanning microscopy (ISM) offers a doubled resolution enhancement in a simple and straightforward manner, based on the commonly used confocal microscopes. ISM is also suitable to be integrated with multi-photon microscopy techniques, such as two-photon excitation and second-harmonic generation imaging, for deep tissue imaging, but it remains the twofold limited resolution enhancement and requires expensive femtosecond lasers. Here, the super-linear ISM (SL-ISM) pushes the resolution enhancement beyond the factor of two is presented and experimentally demonstrated, with a single low-power, continuous-wave, and near-infrared laser, by harnessing the emission nonlinearity within the multiphoton excitation process of lanthanide-doped upconversion nanoparticles (UCNPs). Based on a modified confocal microscope, a resolution of ≈120 nm, 1/8th of the excitation wavelength is achieved. Furthermore, a parallel detection strategy of SL-ISM with the multifocal structured excitation pattern is demonstrated, to speed up the acquisition frame rate. This method suggests a new perspective for super-resolution imaging or sensing, multi-photon imaging, and deep-tissue imaging with simple, low-cost, and straightforward implementations.
KW - ISM
KW - nonlinearity
KW - super-resolution microscopy
KW - upconversion nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85202646577&partnerID=8YFLogxK
U2 - 10.1002/lpor.202400746
DO - 10.1002/lpor.202400746
M3 - Article
AN - SCOPUS:85202646577
SN - 1863-8880
VL - 18
JO - Laser and Photonics Reviews
JF - Laser and Photonics Reviews
IS - 12
M1 - 2400746
ER -