Statistical estimation theory detection limits for label-free imaging

TL;DR

This paper develops a unified statistical estimation framework to evaluate detection limits across various label-free microscopy techniques, enabling comparison of their sensitivity and fundamental constraints on measurement precision.

Contribution

It introduces a comprehensive model and analysis method based on Fisher information and CRLB to compare detection sensitivities of multiple label-free optical imaging modalities.

Findings

Unified framework for evaluating detection limits

Quantitative comparison of sensitivity across modalities

Fundamental bounds on estimation precision established

Abstract

The emergence of label-free microscopy techniques has significantly improved our ability to precisely characterize biochemical targets, enabling non-invasive visualization of cellular organelles and tissue organization. Each label-free method has specific benefits, drawbacks, and varied varied sensitivity under measurement conditions across different types of specimens. To link all these disparate label-free optical interactions together and to compare detection sensitivity of these modalities, we investigate their sensitivity within the framework of statistical estimation theory. This paper introduces a comprehensive unified framework for evaluating the bounds for signal detection with label-free microscopy methods, including second harmonic generation (SHG), third harmonic generation (THG), coherent anti-Stokes Raman scattering (CARS), coherent Stokes Raman scattering (CSRS), stimulated Raman loss (SRL), stimulated Raman gain (SRG), stimulated emission (SE), impulsive stimulated Raman scattering (ISRS), transient absorption (TA), and photothermal effect (PTE). A general model for signal generation induced by optical scattering is developed. Based on this model, the information obtained is quantitatively analyzed using Fisher information, and the fundamental constraints on estimation precision are evaluated through the Cram\'er-Rao Lower Bound (CRLB).