Label-Free Longitudinal Imaging of Single Cell Drug Response with a 3D-Printed Cell Culture Platform

This is the authors' abstract. We don't add key points for this paper.

Image-based phenotypic screening has emerged as a powerful tool for revealing single-cell heterogeneity and dynamic phenotypic responses in preclinical drug discovery. Compared to traditional static end point assays, live-cell longitudinal imaging captures the temporal trajectories of individual cells, including transient morphological adaptations, motility shifts, and divergent subpopulation behaviors, enabling high content features and more robust early prediction of treatment outcomes. Fluorescence-based screening, while highly specific, is constrained in live-cell contexts by broad spectral overlaps (limiting multiplexing to fewer than six channels), bulky fluorophores that may perturb small-molecule interactions, and photobleaching or phototoxicity under repeated excitation. Stimulated Raman scattering (SRS) microscopy overcomes these barriers by delivering label-free, quantitative chemical contrasts alongside morphological information. Here, we present a low-cost, 3D-printed cell culture platform compatible with the stringent optical requirements of an SRS microscope. This setup enables real-time drug delivery and continuous monitoring of biochemical and morphological changes in living cells during 24 h time-lapse imaging with minimal photodamage. We outline a processing pipeline for longitudinal SRS images to extract chemical and morphological features of single live cells. Using this system, we showcase time-lapse SRS microscopy as a tool to map heterogeneous drug-induced single-cell response over time, enabling the identification of varying trajectories within complex cell populations. By parallelizing multiwell perfusion with label-free chemical imaging, our approach provides a pathway toward high-throughput pharmacodynamic assays, accelerating phenotypic screening and personalized medicine.