System Modularity Chip for Analysis of Rare Targets (SMART-Chip): Liquid Biopsy Samples

被引:17
作者
Pahattuge, Thilanga N. [1 ,2 ]
Freed, Ian M. [1 ,2 ]
Hupert, Mateusz L. [3 ]
Vaidyanathan, Swarnagowri [2 ,4 ]
Childers, Katie [2 ,4 ]
Witek, Malgorzata A. [1 ,2 ]
Weerakoon-Ratnayake, Kumuditha [1 ,2 ]
Park, Daniel [2 ,5 ]
Kasi, Anup [6 ]
Al-Kasspooles, Mazin F. [6 ]
Murphy, Michael C. [2 ,5 ]
Soper, Steven A. [1 ,2 ,3 ,4 ,7 ,8 ,9 ]
机构
[1] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
[2] Univ Kansas, Ctr BioModular Multiscale Syst Precis Med, Lawrence, KS 66045 USA
[3] BioFluidica Inc, Lawrence, KS 66045 USA
[4] Univ Kansas, Dept Bioengn, Lawrence, KS 66045 USA
[5] Louisiana State Univ, Dept Mech & Ind Engn, Baton Rouge, LA 70803 USA
[6] Univ Kansas, Dept Med Oncol, Med Ctr, Kansas City, KS 66160 USA
[7] Univ Kansas, Dept Mech Engn, Lawrence, KS 66045 USA
[8] Univ Kansas, Dept Canc Biol, Med Ctr, Kansas City, KS 66160 USA
[9] Univ Kansas, Med Ctr, KU Canc Ctr, Kansas City, KS 66160 USA
关键词
affinity enrichment; circulating tumor cells; immunophenotyping; impedance sensing; integrated modular system; microfluidics; liquid biopsy; CIRCULATING TUMOR-CELLS; CENTRIFUGAL MICROFLUIDIC DEVICE; HIGHLY EFFICIENT; FABRICATION; BLOOD; MICROCHANNELS; ENUMERATION; CLUSTERS; SIZE;
D O I
10.1021/acssensors.0c02728
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Liquid biopsies are becoming popular for managing a variety of diseases due to the minimally invasive nature of their acquisition, thus potentially providing better outcomes for patients. Circulating tumor cells (CTCs) are among the many different biomarkers secured from a liquid biopsy, and a number of efficient platforms for their isolation and enrichment from blood have been reported. However, many of these platforms require manual sample handling, which can generate difficulties when translating CTC assays into the clinic due to potential sample loss, contamination, and the need for highly specialized operators. We report a system modularity chip for the analysis of rare targets (SMART-Chip) composed of three taskspecific modules that can fully automate processing of CTCs. The modules were used for affinity selection of the CTCs from peripheral blood with subsequent photorelease, simultaneous counting, and viability determinations of the CTCs and staining/imaging of the CTCs for immunophenotyping. The modules were interconnected to a fluidic motherboard populated with valves, interconnects, pneumatic control channels, and a fluidic network. The SMART-Chip components were made from thermoplastics via microreplication, which lowers the cost of production making it amenable to clinical implementation. The utility of the SMART-Chip was demonstrated by processing blood samples secured from colorectal cancer (CRC) and pancreatic ductal adenocarcinoma (PDAC) patients. We were able to affinity-select EpCAM expressing CTCs with high purity (0-3 white blood cells/mL of blood), enumerate the selected cells, determine their viability, and immunophenotype the cells. The assay could be completed in <4 h, while manual processing required >8 h.
引用
收藏
页码:1831 / 1839
页数:9
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