High-throughput isolation of fetal nucleated red blood cells by multifunctional microsphere-assisted inertial microfluidics

被引:19
作者
Wang, Zixiang [1 ]
Cheng, Lin [2 ]
Wei, Xiaoyun [1 ]
Cai, Bo [3 ]
Sun, Yue [1 ]
Zhang, Yuanzhen [2 ]
Liao, Lei [1 ]
Zhao, Xing-Zhong [1 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Minist Educ, Key Lab Artificial Micro & Nanostruct, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Obstet & Gynecol, Zhongnan Hosp, Wuhan 430071, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Res Ctr Tissue Engn & Regenerat Med, Union Hosp, Tongji Med Coll, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-invasive prenatal diagnosis; Fetal nucleated red blood cell; High throughput microfluidic chip; Enzymatic release; NONINVASIVE PRENATAL-DIAGNOSIS; CIRCULATING TUMOR-CELLS; MATERNAL BLOOD; CANCER-CELLS; ENRICHMENT; SEPARATION; CAPTURE; RELEASE; CHANNEL; MODEL;
D O I
10.1007/s10544-020-00531-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Being easy, safe and reliable, non-invasive prenatal diagnosis (NIPD) has been greatly pursued in recent years. Holding the complete genetic information of the fetus, fetal nucleated red blood cells (fNRBCs) are viewed as a suitable target for NIPD application. However, effective separating fNRBCs from maternal peripheral blood for clinic use still faces great challenges, given that fNRBCs are extremely rare in maternal blood circulation. Here, by combining the high-throughput inertial microfluidic chip with multifunctional microspheres as size amplification, we develop a novel method to isolate fNRBCs with high performance. To enlarge the size difference between fNRBCs and normal blood cells, we use the gelatin coated microspheres to capture fNRBCs with anti-CD147 as specific recognizer at first. The size difference between fNRBCs captured by the microspheres and normal blood cells makes it easy to purify the captured fNRBCs through the spiral microfluidic chip. Finally, the purified fNRBCs are mildly released from the microspheres by enzymatically degrading the gelatin coating. Cell capture efficiency about 81%, high purity of 83%, as well as cell release viability over 80% were achieved using spiked samples by this approach. Additionally, fNRBCs were successfully detected from peripheral blood of pregnant women with an average of 24 fNRBCs per mL, suggesting the great potential of this method for clinical non-invasive prenatal diagnosis.
引用
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页数:9
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