Auto-ICell: An Automated and Cost-Effective Integrated Droplet Microfluidic Platform for Real-Time Analysis of Single-Cell Morphology and Apoptosis
preprint
OA: closed
Abstract
Abstract Existing single-cell analysis methods based on droplet microfluidics face challenges related to high chip costs and the lack of accurate, time-efficient, and high-throughput analysis techniques. To address these limitations, we present the Auto-ICell, a cost-effective droplet microfluidic system that integrates a 3D-printed microfluidic chip with automated image analysis algorithms. The Auto-ICell enables the generation of uniform droplet reactors and real-time analysis of single-cell morphology and apoptosis. With a throughput of 1,500 droplets per minute and droplet diameters ranging from 70 to 240 μm, the system employs colour-based and deep-learning-enabled algorithms for the analysis of droplet encapsulation and cell morphology, respectively. The Auto-ICell achieves an accuracy of over 91% and processes images in less than 0.03 seconds, eliminating the need for specialized facilities or trained operators. Its versatility extends to applications in cell culture, microreactors, drug carriers, assays, synthetic biology, and diagnostics. This study showcases the potential of the Auto-ICell system in advancing biological research and personalized disease treatment.
My notes (saved in your browser only)
Citation neighborhood (no data yet)
We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.
Source provenance
- europepmc
- last seen: 2026-05-19T01:45:01.086888+00:00