实现高通量细胞力学表征的全自动全息显微系统

Manual operation of microscopes for repetitive tasks in cell biology is a significant bottleneck, consuming invaluable expert time, and introducing human error. Automation is essential, and while Digital Holographic Microscopy (DHM) offers powerful, label-free quantitative phase imaging (QPI), its inherently noisy and low-contrast holograms make robust autofocus and object detection challenging. We present the design, integration, and validation of a fully automated closed-loop DHM system engineered for high-throughput mechanical characterization of biological cells. The system integrates automated serpentine scanning, real-time YOLO-based object detection, and a high-performance, multi-threaded software architecture using pinned memory and SPSC queues. This design enables the GPU-accelerated reconstruction pipeline to run fully in parallel with the 50 fps data acquisition, adding no sequential overhead. A key contribution is the validation of a robust, multi-stage holographic autofocus strategy; we demonstrate that a selected metric (based on a low-pass filter and standard deviation) provides reliable focusing for noisy holograms where conventional methods (e.g., Tenengrad, Laplacian) fail entirely. Performance analysis of the complete system identifies the 2.23-second autofocus operation-not reconstruction-as the primary throughput bottleneck, resulting in a 9.62-second analysis time per object. This work delivers a complete functional platform for autonomous DHM screening and provides a clear, data-driven path for future optimization, proposing a hybrid brightfield imaging modality to address current bottlenecks.