In-Check system: A highly integrated silicon Lab-on-Chip for sample preparation, PCR amplification and microarray detection of nucleic acids directly from biological samples

被引:39
作者
Petralia, Salvatore [1 ]
Verardo, Roberto [2 ,3 ]
Klaric, Enio [2 ,3 ]
Cavallaro, Sebastiano [4 ]
Alessi, Enrico [1 ]
Schneider, Claudio [2 ]
机构
[1] STMicroelectronics, Healthcare Business Dev Unit, I-95121 Catania, Italy
[2] Lab Nazl CIB, I-34149 Trieste, Italy
[3] Proxenia Srl, I-34149 Trieste, Italy
[4] Italian Natl Res Council, Inst Neurol Disorders, Funct Genom Ctr, I-95126 Catania, Italy
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2013年 / 187卷
关键词
Lab-on-Chip; Sample preparation; PCR (polymerase chain reaction); Microarray hybridization; POLYMERASE-CHAIN-REACTION; DNA EXTRACTION; CELL-LYSIS; BIOCHIP; PLATFORM;
D O I
10.1016/j.snb.2012.09.068
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The development of a simple and rapid point-of-care clinical diagnostic device is essential for the evolution of sensing in healthcare technologies. In this study we introduce a fully integrated method for the detection of nucleic acids from cultured human cells and whole blood using the In-Check system supplied by STMicroelectronics. This work represents the first step toward the integration of sample preparation, nucleic acids amplification and DNA microarray detection into a simple and fast silicon Lab-on-Chip system. In particular, we report the experimental results for the detection of the human beta-globine gene (HBB) directly from defined numbers of cultured human cells and whole blood in less than 2 h. The influence of PCR inhibitors was also evaluated when the detection was performed on whole blood. The sample preparation process was entirely performed in a single step in the silicon microreactor, and assessed by RT-qPCR and direct DNA quantification. The extracted DNA, after PCR amplification, was hybridized on the DNA microarray. Both the DNA amount and the amplification efficiency were higher than those obtained with a conventional multi-step process used for comparison. Altogether, the results demonstrate the feasibility of casting a sample preparation step in miniaturized microfluidics systems to develop fully integrated, simple and rapid sample-to-detection nucleic acids-based diagnostic systems. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:99 / 105
页数:7
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