Improvement of Methods for the Isolation of Cell-Free Fetal DNA from Maternal Plasma: Comparison of a Manual and an Automated Method

2006 ◽  
Vol 1075 (1) ◽  
pp. 308-312 ◽  
Author(s):  
D. J HUANG ◽  
B. G ZIMMERMANN ◽  
W. HOLZGREVE ◽  
S. HAHN
2005 ◽  
Vol 51 (12) ◽  
pp. 2419-2420 ◽  
Author(s):  
Dorothy J Huang ◽  
Bernhard G Zimmermann ◽  
Wolfgang Holzgreve ◽  
Sinuhe Hahn

2006 ◽  
Vol 195 (6) ◽  
pp. S174
Author(s):  
Donghyun Cha ◽  
Kyoungjin Lee ◽  
Ji Hyun Park ◽  
Kyoung Joo Lee ◽  
Ji Yeon Kim ◽  
...  

2019 ◽  
Vol 74 (2) ◽  
pp. 61-63
Author(s):  
G. Le Conte ◽  
A. Letourneau ◽  
J. Jani ◽  
P. Kleinfinger ◽  
L. Lohmann ◽  
...  

2009 ◽  
Vol 55 (12) ◽  
pp. 2144-2152 ◽  
Author(s):  
Thomas Hahn ◽  
Klaus S Drese ◽  
Ciara K O'Sullivan

Abstract Background: Routine prenatal diagnosis of chromosomal anomalies is based on invasive procedures, which carry a risk of approximately 1%–2% for loss of pregnancy. An alternative to these inherently invasive techniques is to isolate fetal DNA circulating in the pregnant mother’s plasma. Free fetal DNA circulates in maternal plasma primarily as fragments of lengths <500 bp, with a majority being <300 bp. Separating these fragments by size facilitates an increase in the ratio of fetal to maternal DNA. Methods: We describe our development of a microsystem for the enrichment and isolation of cell-free fetal DNA from maternal plasma. The first step involves a high-volume extraction from large samples of maternal plasma. The resulting 80-μL eluate is introduced into a polymeric microsystem within which DNA is trapped and preconcentrated. This step is followed by a transient isotachophoresis step in which the sample stacks within a neighboring channel for subsequent size separation and is recovered via an outlet at the end of the channel. Results: Recovered fractions of fetal DNA were concentrated 4–8 times over those in preconcentration samples. With plasma samples from pregnant women, we detected the fetal SRY gene (sex determining region Y) exclusively in the fragment fraction of <500 bp, whereas a LEP gene (leptin) fragment was detected in both the shorter and longer recovery fractions. Conclusions: The microdevice we have described has the potential to open new perspectives in noninvasive prenatal diagnosis by facilitating the isolation of fetal DNA from maternal plasma in an integrated, inexpensive, and easy-to-use microsystem.


2014 ◽  
Vol 42 (1) ◽  
pp. 22-28 ◽  
Author(s):  
Elena Picchiassi ◽  
Gian Carlo Di Renzo ◽  
Federica Tarquini ◽  
Vittorio Bini ◽  
Michela Centra ◽  
...  

2014 ◽  
Vol 35 (1) ◽  
pp. 42-45 ◽  
Author(s):  
F. Tarquini ◽  
E. Picchiassi ◽  
M. Centra ◽  
L. Pennacchi ◽  
F. Galeone ◽  
...  

Author(s):  
Nilesh Dharajiya ◽  
Tricia Zwiefelhofer ◽  
Xiaojun Guan ◽  
Vach Angkachatchai ◽  
Juan‐Sebastian Saldivar

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