Isolation of nucleated red blood cells in maternal blood for Non-invasive prenatal diagnosis

2015 ◽  
Vol 17 (6) ◽  
Author(s):  
Yeongje Byeon ◽  
Chang-Seok Ki ◽  
Ki-Ho Han
2001 ◽  
Vol 21 (10) ◽  
pp. 827-834 ◽  
Author(s):  
Lucille Voullaire ◽  
Panayiotis Ioannou ◽  
Sara Nouri ◽  
Robert Williamson

Lab on a Chip ◽  
2018 ◽  
Vol 18 (18) ◽  
pp. 2749-2756 ◽  
Author(s):  
Huimin Zhang ◽  
Yuanyuan Yang ◽  
Xingrui Li ◽  
Yuanzhi Shi ◽  
Bin Hu ◽  
...  

We proposed a FETAL-Chip for efficient enrichment of cNRBCs, which offers great potential for NIPD.


Micromachines ◽  
2019 ◽  
Vol 10 (2) ◽  
pp. 132 ◽  
Author(s):  
Gwo-Chin Ma ◽  
Wen-Hsiang Lin ◽  
Chung-Er Huang ◽  
Ting-Yu Chang ◽  
Jia-Yun Liu ◽  
...  

Circulating fetal cells (CFCs) in maternal blood are rare but have a strong potential to be the target for noninvasive prenatal diagnosis (NIPD). “Cell RevealTM system” is a silicon-based microfluidic platform capable to capture rare cell populations in human circulation. The platform is recently optimized to enhance the capture efficiency and system automation. In this study, spiking tests of SK-BR-3 breast cancer cells were used for the evaluation of capture efficiency. Then, peripheral bloods from 14 pregnant women whose fetuses have evidenced non-maternal genomic markers (e.g., de novo pathogenic copy number changes) were tested for the capture of circulating fetal nucleated red blood cells (fnRBCs). Captured cells were subjected to fluorescent in situ hybridization (FISH) on chip or recovered by an automated cell picker for molecular genetic analyses. The capture rate for the spiking tests is estimated as 88.1%. For the prenatal study, 2–71 fnRBCs were successfully captured from 2 mL of maternal blood in all pregnant women. The captured fnRBCs were verified to be from fetal origin. Our results demonstrated that the Cell RevealTM system has a high capture efficiency and can be used for fnRBC capture that is feasible for the genetic diagnosis of fetuses without invasive procedures.


2000 ◽  
Vol 20 (2) ◽  
pp. 169-171 ◽  
Author(s):  
Zou Li ◽  
Ye Xiaojing ◽  
Xu Keshu ◽  
Zhu Jianwen

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