Magnetic smartphone microflow cytometry enables rapid CD4/CD8 T cell quantification

流式细胞术 微流控 细胞仪 磁珠 微流控芯片 生物医学工程 纳米技术 细胞计数 停流 化学 计算机科学 人类免疫缺陷病毒(HIV) 免疫磁选 材料科学 实验室晶片 生物系统 荧光
作者
Hee Sik Shin,Sung‐Joo Lee,Jae Kim,Jung Ho Kim,Jun Yong Choi,Su Jin Jeong,Sungyoung Choi
出处
期刊:Lab on a Chip [Royal Society of Chemistry]
卷期号:26 (2): 437-447
标识
DOI:10.1039/d5lc00801h
摘要

Accurate enumeration of CD4+ and CD8+ T lymphocytes is essential for HIV management, yet conventional flow cytometry remains largely inaccessible in resource-limited settings. Current point-of-care testing (POCT) approaches, including lateral flow assays and fluorescence-based imaging methods, offer improved accessibility but typically compromise accuracy and yield semi-quantitative results. Here, we present a magnetic-activated smartphone microflow cytometry (MACC) platform that enables rapid, highly accessible, and fully quantitative T lymphocyte counting at the POCT. MACC integrates microfluidic immunomagnetic cell separation with smartphone-based bright-field imaging, providing high-sensitivity, highly accessible analysis without requiring sophisticated laboratory equipment or fluorescent labels. A degassing-driven microfluidic pumping mechanism ensures stable microflow generation for reliable continuous analysis, while smartphone imaging enables clear differentiation of targeted lymphocytes from non-lymphocytes. The complete assay, including magnetic bead labeling, chip operation, hands-on procedures, and automated cell-counting analysis, is completed within 24 min. Validation with HIV-infected patient samples demonstrated strong concordance between MACC and conventional flow cytometry for CD4+ and CD8+ counts as well as CD4/CD8 ratio measurements, with minimal bias. By combining high accessibility, cost-effectiveness, and ease of operation, MACC represents a promising alternative to traditional methods, facilitating decentralized HIV monitoring and expanding diagnostic accessibility in resource-limited settings.
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