Fluorescence Lifetime Imaging (FLI) is a critical molecular imaging modality that provides unique information about the tissue microenvironment, which is invaluable for biomedical applications. FLI operates by acquiring and analyzing photon time-of-arrival histograms to extract quantitative parameters associated with temporal fluorescence decay. These histograms are influenced by the intrinsic properties of the fluorophore, instrument parameters, time-of-flight distributions associated with pixel-wise variations in the topographic and optical characteristics of the sample. Recent advancements in Deep Learning (DL) have enabled improved fluorescence lifetime parameter estimation. However, existing models are primarily designed for planar surface samples, limiting their applicability in translational scenarios involving complex surface profiles, such as \textit{in-vivo} whole-animal or imaged guided surgical applications. To address this limitation, we present MFliNet (Macroscopic FLI Network), a novel DL architecture that integrates the Instrument Response Function (IRF) as an additional input alongside experimental photon time-of-arrival histograms. Leveraging the capabilities of a Differential Transformer encoder-decoder architecture, MFliNet effectively focuses on critical input features, such as variations in photon time-of-arrival distributions. We evaluate MFliNet using rigorously designed tissue-mimicking phantoms and preclinical in-vivo cancer xenograft models. Our results demonstrate the model's robustness and suitability for complex macroscopic FLI applications, offering new opportunities for advanced biomedical imaging in diverse and challenging settings.

Fluorescence lifetime imaging (FLI) is a widely used technique in the biomedical field for measuring the decay times of fluorescent molecules, providing insights into metabolic states, protein interactions, and ligand-receptor bindings. However, its broader application in fast biological processes, such as dynamic activity monitoring, and clinical use, such as in guided surgery, is limited by long data acquisition times and computationally demanding data processing. While deep learning has reduced post-processing times, time-resolved data acquisition remains a bottleneck for real-time applications. To address this, we propose a method to achieve real-time FLI using an FPGA-based hardware accelerator. Specifically, we implemented a GRU-based sequence-to-sequence (Seq2Seq) model on an FPGA board compatible with time-resolved cameras. The GRU model balances accurate processing with the resource constraints of FPGAs, which have limited DSP units and BRAM. The limited memory and computational resources on the FPGA require efficient scheduling of operations and memory allocation to deploy deep learning models for low-latency applications. We address these challenges by using STOMP, a queue-based discrete-event simulator that automates and optimizes task scheduling and memory management on hardware. By integrating a GRU-based Seq2Seq model and its compressed version, called Seq2SeqLite, generated through knowledge distillation, we were able to process multiple pixels in parallel, reducing latency compared to sequential processing. We explore various levels of parallelism to achieve an optimal balance between performance and resource utilization. Our results indicate that the proposed techniques achieved a 17.7x and 52.0x speedup over manual scheduling for the Seq2Seq model and the Seq2SeqLite model, respectively.

Fluorescence lifetime imaging (FLI) is an important technique for studying cellular environments and molecular interactions, but its real-time application is limited by slow data acquisition, which requires capturing large time-resolved images and complex post-processing using iterative fitting algorithms. Deep learning (DL) models enable real-time inference, but can be computationally demanding due to complex architectures and large matrix operations. This makes DL models ill-suited for direct implementation on field-programmable gate array (FPGA)-based camera hardware. Model compression is thus crucial for practical deployment for real-time inference generation. In this work, we focus on compressing recurrent neural networks (RNNs), which are well-suited for FLI time-series data processing, to enable deployment on resource-constrained FPGA boards. We perform an empirical evaluation of various compression techniques, including weight reduction, knowledge distillation (KD), post-training quantization (PTQ), and quantization-aware training (QAT), to reduce model size and computational load while preserving inference accuracy. Our compressed RNN model, Seq2SeqLite, achieves a balance between computational efficiency and prediction accuracy, particularly at 8-bit precision. By applying KD, the model parameter size was reduced by 98\% while retaining performance, making it suitable for concurrent real-time FLI analysis on FPGA during data capture. This work represents a big step towards integrating hardware-accelerated real-time FLI analysis for fast biological processes.