On-line cell lysis and DNA extraction on a microfluidic biochip fabricated by microelectromechanical system technology

被引:30
作者
Chen, Xing [1 ]
Cui, Da Fu [1 ]
Liu, Chang Chun [1 ]
机构
[1] Chinese Acad Sci, Inst Elect, State Key Lab Tranducer Technol, Beijing 100080, Peoples R China
关键词
cell lysis; DNA extraction; microfluidic biochip; porous silicon;
D O I
10.1002/elps.200700551
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Integrating cell lysis and DNA purification process into a micrototal analytical system (mu TAS) is one critical step for the analysis of nucleic acids. On-chip cell lysis based on a chemical method is realized by sufficient blend of blood sample and the lyzing reagent. In this paper two mixing models, T-type mixing model and sandwich-type mixing model, are proposed and simulation of those models is conducted. Result of simulation shows that the sandwich-type mixing model with coiled channel performs best and this model is further used to construct the microfluidic biochip for on-line cell lysis and DNA extraction. The result of simulation is further verified by experiments. It asserts that more than 80% mixing of blood sample and lyzing reagent which guarantees that completed cell lysis can be achieved near the inlet location when the cell/buffer velocity ratio is less than 1:5. After cell lysis, DNA extraction by means of a solid-phase method is implemented by using porous silicon matrix which is integrated in the biochip. During continuous flow process in the microchip, rapid cell lysis and PCR-amplifiable genomic DNA purification can be achieved within 20 min. The potential of this microfluidic biochip is illustrated by pretreating a whole blood sample, which shows the possibility of integration of sample preparation, PCR, and separation on a single device to work as portable point-of-care medical diagnostic system.
引用
收藏
页码:1844 / 1851
页数:8
相关论文
共 30 条
[1]   Improved resolution with microchip-based enhanced field inversion electrophoresis [J].
Backhouse, CJ ;
Gajdal, A ;
Pilarski, LM ;
Crabtree, HJ .
ELECTROPHORESIS, 2003, 24 (11) :1777-1786
[2]   A microfluidic cartridge to prepare spores for PCR analysis [J].
Belgrader, P ;
Okuzumi, M ;
Pourahmadi, F ;
Borkholder, DA ;
Northrup, MA .
BIOSENSORS & BIOELECTRONICS, 2000, 14 (10-11) :849-852
[3]   Microchip-based purification of DNA from biological samples [J].
Breadmore, MC ;
Wolfe, KA ;
Arcibal, IG ;
Leung, WK ;
Dickson, D ;
Giordano, BC ;
Power, ME ;
Ferrance, JP ;
Feldman, SH ;
Norris, PM ;
Landers, JP .
ANALYTICAL CHEMISTRY, 2003, 75 (08) :1880-1886
[4]   Nucleic acid purification using microfabricated silicon structures [J].
Cady, NC ;
Stelick, S ;
Batt, CA .
BIOSENSORS & BIOELECTRONICS, 2003, 19 (01) :59-66
[5]   Fabrication of solid phase extraction deoxyribonucleic acid chips based on bio-microelectron-mechanical system technology [J].
Chen, X ;
Cui, DF ;
Liu, CC ;
Cai, HY .
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2006, 34 (03) :433-436
[6]   Microfabrication and characterization of porous channels for DNA purification [J].
Chen, Xing ;
Cui, Da-Fu ;
Liu, Chang-Chun ;
Li, Hui .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2007, 17 (01) :68-75
[7]   Rapid, automated nucleic acid probe assays using silicon microstructures for nucleic acid concentration [J].
Christel, LA ;
Petersen, K ;
McMillan, W ;
Northrup, MA .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1999, 121 (01) :22-27
[8]  
COPP MU, 1998, SCIENCE, V280, P1046
[9]   Reagentless mechanical cell lysis by nanoscale barbs in microchannels for sample preparation [J].
Di Carlo, D ;
Jeong, KH ;
Lee, LP .
LAB ON A CHIP, 2003, 3 (04) :287-291
[10]   Influence of surface heterogeneity on electrokinetically driven microfluidic mixing [J].
Erickson, D ;
Li, DQ .
LANGMUIR, 2002, 18 (05) :1883-1892