Microchip module for blood sample preparation and nucleic acid amplification reactions

被引:97
作者
Yuen, PK
Kricka, LJ [1 ]
Fortina, P
Panaro, NJ
Sakazume, T
Wilding, P
机构
[1] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Lab Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[5] Hitachi Ltd, Instrument Div, Hitachinaka, Ibaraki 3128504, Japan
关键词
D O I
10.1101/gr.155301
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
A computer numerical control-machined plexiglas-based microchip module was designed and constructed for the integration of blood sample preparation and nucleic acid amplification reactions. The microchip module is comprised of a custom-made heater-cooler for thermal cycling, a series of 254 mum x 254 mum microchannels for transporting human whole blood and reagents in and out of an 8-9 muL dual-purpose (cell isolation and PCR) glass-silicon microchip. White blood cells were first isolated from a small volume of human whole blood (<3 <mu>L) in an integrated cell isolation-PCR microchip containing a series of 3.5-mum feature-sized "weir-type" filters, formed by an etched silicon dam spanning the flow chamber. A genomic target, a region in the human coagulation Factor V gene (226-bp), was subsequently directly amplified by microchip-based PCR on DNA released from white blood cells isolated on the filter section of the microchip mounted onto the microchip module. The microchip module provides a convenient means to simplify nucleic acid analyses by integrating two key steps in genetic testing procedures, cell isolation and PCR and promises to be adaptable for additional types of integrated assays.
引用
收藏
页码:405 / 412
页数:8
相关论文
共 18 条
[1]   A miniature integrated device for automated multistep genetic assays [J].
Anderson, Rolfe C. ;
Su, Xing ;
Bogdan, Gregory J. ;
Fenton, Jeffery .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12)
[2]  
BRODY JP, 1995, P 8 INT C SOL STAT S, V9, P779
[3]  
BROWN S, 1999, FORTUNE 1011, P282
[4]   An integrated nanoliter DNA analysis device [J].
Burns, MA ;
Johnson, BN ;
Brahmasandra, SN ;
Handique, K ;
Webster, JR ;
Krishnan, M ;
Sammarco, TS ;
Man, PM ;
Jones, D ;
Heldsinger, D ;
Mastrangelo, CH ;
Burke, DT .
SCIENCE, 1998, 282 (5388) :484-487
[5]  
Cheng, 1996, Mol Diagn, V1, P183, DOI 10.1016/S1084-8592(96)70004-8
[6]   Chip PCR .2. Investigation of different PCR amplification systems in microfabricated silicon-glass chips [J].
Cheng, J ;
Shoffner, MA ;
Hvichia, GE ;
Kricka, LJ ;
Wilding, P .
NUCLEIC ACIDS RESEARCH, 1996, 24 (02) :380-385
[7]   Analysis of ligase chain reaction products amplified in a silicon-glass chip using capillary electrophoresis [J].
Cheng, J ;
Shoffner, MA ;
Mitchelson, KR ;
Kricka, LJ ;
Wilding, P .
JOURNAL OF CHROMATOGRAPHY A, 1996, 732 (01) :151-158
[8]  
Cheng J, 1998, TOP CURR CHEM, V194, P215
[9]  
CHENG J, 1995, FRED C CAP EL FRED M
[10]  
FIEHN H, 1995, MESA MG, P289