TY - JOUR
T1 - An integrated chip capable of performing sample pretreatment and nucleic acid amplification for HIV-1 detection
AU - Wang, Jung Hao
AU - Cheng, Lie
AU - Wang, Chih Hung
AU - Ling, Wei Shuo
AU - Wang, Shainn Wei
AU - Lee, Gwo Bin
N1 - Funding Information:
The authors gratefully acknowledge the National Science Council of Taiwan ( NSC 99-2218-E-006-234 ; NSC 100-2120-M-007-014 ), the “ Towards A World-class University ” Project and the Multidisciplinary Center of Excellence for Clinical Trial and Research ( DOH101-TD-B-111-102 ), Department of Health, Executive Yuan, Taiwan , for providing financial support for this study.
PY - 2013/3/15
Y1 - 2013/3/15
N2 - This study reports on a microfluidic system equipped with a sample pretreatment device and a nucleic acid amplification device for the rapid diagnosis of the human immunodeficiency virus-1 (HIV-1). The system analyzed proviral deoxyribonucleic acid (DNA) from an HIV-infected Jurkat T cell line. In order to ensure accurate diagnosis among other prevalent B-type strains, simultaneous detections of four conserved HIV-1 B-type DNA fragments were performed in this integrated microfluidic system. The entire protocol including cell lysis, extraction of DNA, polymerase chain reaction (PCR), and optical detection were successfully integrated in order to perform a rapid, automated diagnosis. Experimental results showed that four primer sets with conserved HIV-1 B-type sequences specific for the 167-bp RU5 promoter region, the 424-bp int, the 117-bp tat, and the 162-bp vpr coding regions were successfully amplified from the respective regions of the proviral DNA, even from a single infected cell. This accurate real-time detection was achieved within 95. min using the integrated optical system.
AB - This study reports on a microfluidic system equipped with a sample pretreatment device and a nucleic acid amplification device for the rapid diagnosis of the human immunodeficiency virus-1 (HIV-1). The system analyzed proviral deoxyribonucleic acid (DNA) from an HIV-infected Jurkat T cell line. In order to ensure accurate diagnosis among other prevalent B-type strains, simultaneous detections of four conserved HIV-1 B-type DNA fragments were performed in this integrated microfluidic system. The entire protocol including cell lysis, extraction of DNA, polymerase chain reaction (PCR), and optical detection were successfully integrated in order to perform a rapid, automated diagnosis. Experimental results showed that four primer sets with conserved HIV-1 B-type sequences specific for the 167-bp RU5 promoter region, the 424-bp int, the 117-bp tat, and the 162-bp vpr coding regions were successfully amplified from the respective regions of the proviral DNA, even from a single infected cell. This accurate real-time detection was achieved within 95. min using the integrated optical system.
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U2 - 10.1016/j.bios.2012.09.011
DO - 10.1016/j.bios.2012.09.011
M3 - Article
C2 - 23083906
AN - SCOPUS:84870777027
SN - 0956-5663
VL - 41
SP - 484
EP - 491
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 1
ER -