Abstract

Superresolution (SR) optical microscopy has allowed the investigation of many biological structures below the diffraction limit; however, most of the techniques are hampered by the need for fluorescent labels. Nonlinear label-free techniques such as second-harmonic generation (SHG) provide structurally specific contrast without the addition of exogenous labels, allowing observation of unperturbed biological systems. We use the photonic nanojet (PNJ) phenomena to achieve SR-SHG. A resolution of with respect to the fundamental wavelength, that is, a -fold improvement over conventional or diffraction-limited SHG under the same imaging conditions is achieved. Crucially we find that the polarization properties of excitation are maintained in a PNJ. This is observed in experiment and simulations. This may have widespread implications to increase sensitivity by detection of polarization-resolved SHG by observing anisotropy in signals. These new, to the best of our knowledge, findings allowed us to visualize biological SHG-active structures such as collagen at an unprecedented and previously unresolvable spatial scale. Moreover, we demonstrate that the use of an array of self-assembled high-index spheres overcomes the issue of a limited field of view for such a method, allowing PNJ-assisted SR-SHG to be used over a large area. Dysregulation of collagen at the nanoscale occurs in many diseases and is an underlying cause in diseases such as lung fibrosis. Here we demonstrate that pSR-SHG allows unprecedented observation of changes at the nanoscale that are invisible by conventional diffraction-limited SHG imaging. The ability to nondestructively image SHG-active biological structures without labels at the nanoscale with a relatively simple optical method heralds the promise of a new tool to understand biological phenomena and drive drug discovery.

Highlights

  • The Abbe “diffraction limit” states that the resolution of an optical microscope is limited by its wavelength to ∼λ/(2NA), with NA being the numerical aperture of the imaging system

  • Since signal-to-noise ratio (SNR) is inherently linked to resolution, further experiments were conducted at the highest excitation power possible within the damage threshold of the sample to obtain the highest resolution within the imaging conditions

  • While imaging in the far field, we show that near-field components of the photonic nanojet (PNJ) contribute to the subdiffraction-limited spot sizes to enable SR-SHG observed with this method

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Summary

INTRODUCTION

The Abbe “diffraction limit” states that the resolution of an optical microscope is limited by its wavelength to ∼λ/(2NA), with NA being the numerical aperture of the imaging system. Many techniques exist to surpass this limit, both in the far field: stimulated emission depletion (STED) microscopy, localization microscopies such as PALM/STORM, structured illumination microscopy (SIM) and in the near field: near-field scanning optical. Such as barium titanate (BaTiO3) and biological macromolecules including the actin-myosin complex, microtubules, and fibrillar collagen. The ability to perform far-field label-free SHG imaging with subdiffraction-limited resolution holds significant potential for biomedical research, as changes in collagen structure and function underlie many diseases including fibrosis and cancers. Our work heralds the role that label-free SR techniques can play to unravel underlying biological phenomena and improve our understanding of disease mechanisms

RESULTS AND DISCUSSION
CONCLUSIONS
SHG Imaging System
Lung Tissue
Spheroid Sample Preparation
SHG Resolution Standard Fabrication
Simulations
10. Calculation of Polarization Anisotropy
11. Collagen Fiber Analysis
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