Recent Advances of Microfluidic Platform for Cell Based Non-Invasive Prenatal Diagnosis

被引:2
|
作者
Jou, Hei-Jen [1 ,2 ,3 ,4 ]
Lo, Pei-Hsuan [1 ]
Ling, Pei-Ying [1 ]
机构
[1] Taiwan Adventist Hosp, Dept Obstet & Gynecol, Taipei 105404, Taiwan
[2] Natl Taipei Univ Nursing & Hlth Sci, Sch Nursing, Taipei 112303, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Obstet & Gynecol, Taipei 100225, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Int Coll Semicond Technol, Hsinchu 300093, Taiwan
关键词
non-invasive prenatal diagnosis; circulating fetal cells; extravillous trophoblasts; fetal nucleated RBCs; microfluidic devices; immunoaffinity; size-based microfluidics; FETAL CELLS; MATERNAL BLOOD; DNA; ACCURACY;
D O I
10.3390/ijms24020991
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of the present review is to try to highlight recent advances in the application of microfluidic technology on non-invasive prenatal diagnosis (NIPD). The immunoaffinity based microfluidic technology is the most common approach for NIPD, followed by size-based microfluidic methods. Immunoaffinity microfluidic methods can enrich and isolate circulating fetal extravillous trophoblasts (fEVTs) or fetal nucleated red blood cells (fnRBCs) for NIPD by using specific antibodies, but size-based microfluidic systems are only applied to isolate fEVTs. Most studies based on the immunoaffinity microfluidic system gave good results. Enough fetal cells were obtained for chromosomal and/or genetic analysis in all blood samples. However, the results from studies using size-based microfluidic systems for NIPD are less than ideal. In conclusion, recent advances in microfluidic devices make the immunoaffinity based microfluidic system potentially a powerful tool for cell-based NIPD. However, more clinical validation is needed.
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页数:8
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