Center for Engineering in Medicine and Surgery, Massachusetts General Hospital, Boston, MA, 02129, USA.
Harvard Medical School, Boston, MA, 02115, USA.
Adv Sci (Weinh). 2024 Oct;11(40):e2405853. doi: 10.1002/advs.202405853. Epub 2024 Aug 28.
Screening liters of blood (i.e., apheresis) represents a generalized approach to promote the reliable access to circulating tumor cell clusters (CTCCs), which are known to be highly metastasis-competent, yet ultrarare. However, no existing CTCC sorting technology has demonstrated high throughput, high yield, low shear stress, and minimal blood dilution simultaneously as required in apheresis. Here, a label-free method is introduced termed Precision Apheresis for Non-invasive Debulking of cell Aggregates (PANDA) to continuously isolate CTCCs from undiluted blood to clean buffer through size sorting, processing 1.4 billion cells per second. The cell focusing is optimized within whole blood leveraging secondary transverse flow and margination. The PANDA chip recovers >90% of spiked ≈24 rare HeLa cell clusters from 100 mL undiluted blood samples (equivalent to ≈500 billion blood cells) at 1 L h throughput, with ≤20s device residence time, ≤15 Pa shear stress, and >99.9% return of blood components. The technology lays the groundwork for future routine isolation to increase the recovery of these ultrarare yet clinically significant tumor cell populations from large volumes of blood to advance cancer research, early detection, and treatment.
从数升血液(即细胞单采术)中筛选,代表了一种广义的方法,旨在促进循环肿瘤细胞簇(CTCC)的可靠获取,这些细胞簇已知具有高度转移能力,但极为罕见。然而,现有的 CTCC 分选技术尚未证明能够同时实现高通量、高产量、低剪切应力和最小的血液稀释,而这些都是细胞单采术所必需的。在这里,引入了一种无标记方法,称为用于非侵入性细胞聚集体去块的精准细胞单采术(PANDA),通过大小分选,从未稀释的血液连续分离 CTCC 到清洁缓冲液,每秒处理 14 亿个细胞。在全血中,细胞聚焦通过二次横向流和靠边作用得到优化。该 PANDA 芯片以 1 L/h 的吞吐量,从 100 mL 未稀释的血液样本(相当于 ≈5000 亿个血细胞)中回收了超过 90%的 ≈24 个稀有的 HeLa 细胞簇,设备停留时间≤20s,剪切应力≤15 Pa,血液成分的回收率>99.9%。该技术为未来的常规分离奠定了基础,可从大量血液中增加这些极为罕见但具有临床意义的肿瘤细胞群的回收率,从而推进癌症研究、早期检测和治疗。