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Non-invasive Prenatal Diagnosis of Chromosomal Aneuploidies and Microdeletion Syndrome Using Fetal Nucleated Red Blood Cells Isolated by Nanostructure Microchips

机译:纳米结构芯片分离的胎儿有核红细胞对染色体非整倍性和微缺失综合征的非侵入性产前诊断。

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摘要

Detection of detached fetal nucleated red blood cells (fNRBCs) in the maternal peripheral blood may serve as a prospective testing method competing with the cell-free DNA, in non-invasive prenatal testing (NIPT).>Methods: Herein, we introduce a facile and effective lab-on-a-chip method of fNRBCs detection using a capture-releasing material that is composed of biotin-doped polypyrrole nanoparticles. To enhance local topographic interactions between the nano-components and fNRBC, a specific antibody, CD147, coated on the nanostructured substrate led to the isolation of fNRBCs from maternal peripheral blood. Subsequently, an electrical system was employed to release the captured cells using 0.8 V for 15 s. The diagnostic application of fNRBCs for fetal chromosomal disorders (Trisomy 13/21/18/X syndrome, microdeletion syndrome) was demonstrated.>Results: Cells captured by nanostructured microchips were identified as fNRBCs. Twelve cases of chromosomal aneuploidies and one case of 18q21 microdeletion syndrome were diagnosed using the fNRBCs released from the microchips.>Conclusion: Our method offers effective and accurate analysis of fNRBCs for comprehensive NIPT to monitor fetal cell development.
机译:在非侵入性产前检查(NIPT)中,检测母体外周血中分离的胎儿有核红细胞(fNRBC)可能是与无细胞DNA竞争的前瞻性检查方法。>方法:在这里,我们介绍了一种简便有效的fNRBCs芯片检测实验室方法,该方法使用了由生物素掺杂的聚吡咯纳米颗粒组成的释放释放材料。为了增强纳米组分与fNRBC之间的局部拓扑相互作用,包被在纳米结构化基质上的特异性抗体CD147导致从母体外周血中分离出fNRBC。随后,采用电气系统以0.8 V的电压释放捕获的细胞15 s。证明了fNRBCs在胎儿染色体疾病(三体性13/21/18 / X综合征,微缺失综合征)中的诊断应用。>结果:纳米结构的微芯片捕获的细胞被鉴定为fNRBCs。使用从微芯片释放的fNRBCs诊断出12例染色体非整倍体病例和1例18q21微缺失综合征。>结论:我们的方法可对fNRBCs进行有效,准确的分析,以进行综合NIPT监测胎儿细胞的发育。

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