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

Verfasser / Beitragende:
[Yeongje Byeon, Chang-Seok Ki, Ki-Ho Han]
Ort, Verlag, Jahr:
2015
Enthalten in:
Biomedical Microdevices, 17/6(2015-12-01), 1-7
Format:
Artikel (online)
ID: 605479593
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024 7 0 |a 10.1007/s10544-015-0021-3  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10544-015-0021-3 
245 0 0 |a Isolation of nucleated red blood cells in maternal blood for Non-invasive prenatal diagnosis  |h [Elektronische Daten]  |c [Yeongje Byeon, Chang-Seok Ki, Ki-Ho Han] 
520 3 |a This paper introduces a two-step cascade enrichment method for isolating nucleated red blood cells (NRBCs) in maternal blood. The two-step enrichment platform consists of a positive enrichment process based on a red blood cell (RBC) hyperaggregation method and a negative enrichment process using microfluidic technology. An analytical evaluation using blood samples from patients with leukemia showed that the while blood cell (WBC) depletion and NRBC loss rates of the positive enrichment process were 93.98% and 6.02%, respectively. Through the two-step cascade enrichment method, 1-396 NRBCs and only 0-6 WBCs were isolated from 1mL of 18 maternal blood samples. Experimental results also showed that the WBC depletion rate of the proposed two-step method was more than 625,000-fold, and the purity of enriched NRBCs ranged from 20% to 100%. Furthermore, SRY (the sex-determining region of the Y chromosome) genes were detected in enriched NRBCs, thereby demonstrating that enriched NRBCs contain fetus-derived NRBCs. 
540 |a Springer Science+Business Media New York, 2015 
690 7 |a Nucleated red blood cells  |2 nationallicence 
690 7 |a Prenatal diagnosis  |2 nationallicence 
690 7 |a RBC hyperaggregation  |2 nationallicence 
690 7 |a Lateral magnetophoretic microseparator  |2 nationallicence 
690 7 |a Microfluidic device  |2 nationallicence 
700 1 |a Byeon  |D Yeongje  |u Department of Nano Science and Engineering, Center for Nano Manufacturing, Inje University, 607 Obang-dong, 621-749, Gimhae, Gyongnam, Republic of Korea  |4 aut 
700 1 |a Ki  |D Chang-Seok  |u Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, 135-710, Gangnam-gu, Seoul, Republic of Korea  |4 aut 
700 1 |a Han  |D Ki-Ho  |u Department of Nano Science and Engineering, Center for Nano Manufacturing, Inje University, 607 Obang-dong, 621-749, Gimhae, Gyongnam, Republic of Korea  |4 aut 
773 0 |t Biomedical Microdevices  |d Springer US; http://www.springer-ny.com  |g 17/6(2015-12-01), 1-7  |x 1387-2176  |q 17:6<1  |1 2015  |2 17  |o 10544 
856 4 0 |u https://doi.org/10.1007/s10544-015-0021-3  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10544-015-0021-3  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Byeon  |D Yeongje  |u Department of Nano Science and Engineering, Center for Nano Manufacturing, Inje University, 607 Obang-dong, 621-749, Gimhae, Gyongnam, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ki  |D Chang-Seok  |u Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, 135-710, Gangnam-gu, Seoul, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Han  |D Ki-Ho  |u Department of Nano Science and Engineering, Center for Nano Manufacturing, Inje University, 607 Obang-dong, 621-749, Gimhae, Gyongnam, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Biomedical Microdevices  |d Springer US; http://www.springer-ny.com  |g 17/6(2015-12-01), 1-7  |x 1387-2176  |q 17:6<1  |1 2015  |2 17  |o 10544