Shields C Wyatt, Ohiri Korine A, Szott Luisa M, López Gabriel P
NSF Research Triangle Materials Research Science and Engineering Center, Duke University, Durham, North Carolina, 27708.
Department of Biomedical Engineering, Duke University, Durham, North Carolina, 27708.
Cytometry B Clin Cytom. 2017 Mar;92(2):115-125. doi: 10.1002/cyto.b.21388. Epub 2016 Jul 5.
Advances in microfluidic cell sorting have revolutionized the ways in which cell-containing fluids are processed, now providing performances comparable to, or exceeding, traditional systems, but in a vastly miniaturized format. These technologies exploit a wide variety of physical phenomena to manipulate cells and fluid flow, such as magnetic traps, sound waves and flow-altering micropatterns, and they can evaluate single cells by immobilizing them onto surfaces for chemotherapeutic assessment, encapsulate cells into picoliter droplets for toxicity screenings and examine the interactions between pairs of cells in response to new, experimental drugs. However, despite the massive surge of innovation in these high-performance lab-on-a-chip devices, few have undergone successful commercialization, and no device has been translated to a widely distributed clinical commodity to date. Persistent challenges such as an increasingly saturated patent landscape as well as complex user interfaces are among several factors that may contribute to their slowed progress. In this article, we identify several of the leading microfluidic technologies for sorting cells that are poised for clinical translation; we examine the principal barriers preventing their routine clinical use; finally, we provide a prospectus to elucidate the key criteria that must be met to overcome those barriers. Once established, these tools may soon transform how clinical labs study various ailments and diseases by separating cells for downstream sequencing and enabling other forms of advanced cellular or sub-cellular analysis. © 2016 International Clinical Cytometry Society.
微流控细胞分选技术的进步彻底改变了含细胞流体的处理方式,如今其性能可与传统系统相媲美甚至超越传统系统,且具备大幅微型化的特点。这些技术利用多种物理现象来操控细胞和流体流动,如磁阱、声波和改变流动的微图案,它们能通过将单细胞固定在表面进行化疗评估来对其进行评估,将细胞封装到皮升液滴中进行毒性筛查,并研究成对细胞在新型实验药物作用下的相互作用。然而,尽管这些高性能芯片实验室设备创新大量涌现,但很少有设备成功实现商业化,迄今为止也没有一种设备转化为广泛应用的临床产品。诸如专利格局日益饱和以及用户界面复杂等持续存在的挑战是导致其进展缓慢的几个因素。在本文中,我们确定了几种有望实现临床转化的领先细胞分选微流控技术;我们研究了阻碍其常规临床应用的主要障碍;最后,我们提供了一份计划书,阐明克服这些障碍必须满足的关键标准。一旦确立,这些工具可能很快会改变临床实验室研究各种疾病的方式,通过分离细胞进行下游测序并实现其他形式的先进细胞或亚细胞分析。 © 2016国际临床细胞计量学会