Time-of-flight fluorescence depth mapping using a spatiotemporal deep learning model.

IF 3.3 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Journal of Biomedical Optics Pub Date : 2026-06-01 Epub Date: 2026-06-18 DOI:10.1117/1.JBO.31.6.066003
Shiru Wang, Arthur Pétusseau, Claudio Bruschini, Edoardo Charbon, Petr Bruza
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引用次数: 0

Abstract

Significance: Fluorescence-guided surgery (FGS) utilizes molecular contrast agents to highlight critical structures or pathological tissues in real time. The premise of FGS is to enable precise surgical decision-making through accurate visualization and quantitative assessment of fluorophore distribution. However, strong effects of diffusion and absorption of fluorescent light in tissue confound fluorescence images, preventing accurate quantitative assessment of the concentration and distribution of fluorescent markers. These optical artifacts may lead to misinterpretation of tissue boundaries and compromised surgical precision, thereby diminishing the capabilities of FGS. Resolving topological depth maps of fluorophore distribution at the millimeter scale is an important first step in performing quantitative sub-surface fluorescence imaging.

Aim: In this study, we present a spatiotemporal deep learning architecture that utilizes picosecond single-photon avalanche diode (SPAD) sensor images to rapidly recover the depth topology of a fluorophore distribution embedded in diffuse media. The network is designed to work with wide-field, epi-illumination geometry and millimeter spatial resolution.

Approach: A ConvLSTM-UNet deep learning network was developed for picosecond time-resolved image analysis. This network was trained on 5000 spatiotemporal maps simulated by the optical Monte Carlo method and convolved with the instrument response function (IRF) of the imaging system. The experimental setup utilized a SwissSPAD2 sensor synchronized with a 635 nm picosecond laser diode. Using only 10 selected temporal gates as input, the network could recover depth maps. Reconstruction accuracy was evaluated using mean error metrics across various depths and background concentrations of a fluorophore with a simulated decay time of 100 ps.

Results: A total of 75 different test fluorescence video data were evaluated. This set encompassed 15 unique inclusion shapes at five different depths. The network successfully reconstructed fluorescence topography up to 15 mm with a mean absolute error of less than 0.6 mm and mean depth variances below 0.5 mm. The inference time was ∼ 30    ms .

Conclusions: Integrating temporal and spatial deep learning networks enabled depth mapping from time-resolved fluorescence data. Utilizing real IRF proved the applicability of SPAD sensors for sub-surface fluorescence mapping.

使用时空深度学习模型的飞行时间荧光深度映射。
意义:荧光引导手术(FGS)利用分子造影剂实时突出关键结构或病理组织。FGS的前提是通过对荧光团分布的精确可视化和定量评估,实现精确的手术决策。然而,荧光在组织中的强烈扩散和吸收影响混淆了荧光图像,妨碍了对荧光标记物浓度和分布的准确定量评估。这些光学伪影可能导致对组织边界的误解和手术精度的降低,从而降低FGS的能力。在毫米尺度上解析荧光团分布的拓扑深度图是进行定量亚表面荧光成像的重要第一步。目的:在本研究中,我们提出了一种时空深度学习架构,该架构利用皮秒单光子雪崩二极管(SPAD)传感器图像快速恢复嵌入漫射介质中的荧光团分布的深度拓扑结构。该网络设计用于宽视场、外延照度几何和毫米空间分辨率。方法:开发了一种用于皮秒时间分辨图像分析的ConvLSTM-UNet深度学习网络。该网络以光学蒙特卡罗方法模拟的5000张时空图为样本进行训练,并与成像系统的仪器响应函数(IRF)进行卷积。实验装置采用与635 nm皮秒激光二极管同步的SwissSPAD2传感器。仅使用10个选定的时间门作为输入,网络就可以恢复深度图。利用模拟衰减时间为100 ps的荧光团不同深度和背景浓度的平均误差度量来评估重建精度。结果:总共评估了75种不同的测试荧光视频数据。这一套包含了15个独特的形状,在五个不同的深度。该网络成功地重建了高达15毫米的荧光地形,平均绝对误差小于0.6毫米,平均深度方差小于0.5毫米。推断时间为~ 30 ms。结论:整合时间和空间深度学习网络可以从时间分辨荧光数据中进行深度映射。利用真实的红外光谱验证了SPAD传感器在地下荧光成像中的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
5.70%
发文量
263
审稿时长
2 months
期刊介绍: The Journal of Biomedical Optics publishes peer-reviewed papers on the use of modern optical technology for improved health care and biomedical research.
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