Abstract
Recently, many resolution enhancing techniques are demonstrated, but most of them are severely limited for deep tissue applications. For example, wide-field based localization techniques lack the ability of optical sectioning, and structured light based techniques are susceptible to beam distortion due to scattering/aberration. Saturated excitation (SAX) microscopy, which relies on temporal modulation that is less affected when penetrating into tissues, should be the best candidate for deep-tissue resolution enhancement. Nevertheless, although fluorescence saturation has been successfully adopted in SAX, it is limited by photobleaching, and its practical resolution enhancement is less than two-fold. Recently, we demonstrated plasmonic SAX which provides bleaching-free imaging with three-fold resolution enhancement. Here we show that the three-fold resolution enhancement is sustained throughout the whole working distance of an objective, i.e., 200 μm, which is the deepest super-resolution record to our knowledge, and is expected to extend into deeper tissues. In addition, SAX offers the advantage of background-free imaging by rejecting unwanted scattering background from biological tissues. This study provides an inspirational direction toward deep-tissue super-resolution imaging and has the potential in tumor monitoring and beyond.
Highlights
Resolution and penetration depths are two key factors in far-field optical imaging of biological tissues
The examples of a stochastic approach are photo-activated localization microscopy (PALM)[2] and stochastic optical reconstruction microscopy (STORM),[3] which are based on wide-field imaging schemes, and lack the ability of optical sectioning, in turn ineffective for deep tissue applications
For deterministic resolution enhancement approaches, such as stimulated emission depletion (STED)[5] microscopy and ground state depletion (GSD)[8] microscopy, they are based on confocal detection and provide optical sectioning for tissue imaging
Summary
Resolution and penetration depths are two key factors in far-field optical imaging of biological tissues. Resolution enhancement in deep-tissue nanoparticle imaging based on plasmonic saturated excitation microscopy
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