基于相量的时域荧光寿命成像显微镜的不确定度定量。

IF 3.2 2区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Biomedical optics express Pub Date : 2025-07-08 eCollection Date: 2025-08-01 DOI:10.1364/BOE.565990
Qinyi Chen, Jongchan Park, Shuqi Mu, Liang Gao
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引用次数: 0

摘要

时域荧光寿命成像显微镜(FLIM)的相量方法为分析复杂的荧光衰减信号提供了一种强大的、无拟合的方法。然而,它的定量精度从根本上受到噪声的限制,特别是光子发射噪声,这在寿命估计和荧光团分离中引入了可变性和偏差。在这项研究中,我们提出了一个基于相量的时域FLIM的理论不确定性模型,该模型可以解析地捕获散粒噪声的传播,并量化其对相量坐标和荧光团权重估计的影响。我们使用蒙特卡罗模拟和从标准荧光染料和生物组织样本中获得的实验数据来验证该模型。我们的模型提高了基于相量的时域FLIM的整体可靠性和效率,特别是在光子限制成像应用中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantifying uncertainty in phasor-based time-domain fluorescence lifetime imaging microscopy.

The phasor approach to time-domain fluorescence lifetime imaging microscopy (FLIM) offers a powerful, fit-free method for analyzing complex fluorescence decay signals. However, its quantitative accuracy is fundamentally limited by noise-particularly photon shot noise-which introduces variability and deviations in lifetime estimation and fluorophore unmixing. In this study, we present a theoretical uncertainty model for phasor-based time-domain FLIM that analytically captures the propagation of shot noise and quantifies its impact on phasor coordinates and fluorophore weight estimation. We validate the model using Monte Carlo simulations and experimental data acquired from standard fluorescent dyes and biological tissue samples. Our model improves the overall reliability and efficiency of phasor-based time-domain FLIM, particularly in photon-limited imaging applications.

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来源期刊
Biomedical optics express
Biomedical optics express BIOCHEMICAL RESEARCH METHODS-OPTICS
CiteScore
6.80
自引率
11.80%
发文量
633
审稿时长
1 months
期刊介绍: The journal''s scope encompasses fundamental research, technology development, biomedical studies and clinical applications. BOEx focuses on the leading edge topics in the field, including: Tissue optics and spectroscopy Novel microscopies Optical coherence tomography Diffuse and fluorescence tomography Photoacoustic and multimodal imaging Molecular imaging and therapies Nanophotonic biosensing Optical biophysics/photobiology Microfluidic optical devices Vision research.
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