4.3 Article

On-chip analysis of respiratory viruses from nasopharyngeal samples

期刊

BIOMEDICAL MICRODEVICES
卷 13, 期 5, 页码 819-827

出版社

SPRINGER
DOI: 10.1007/s10544-011-9552-4

关键词

Lab-on-a-chip; Point-of-care diagnostics; Analysis of respiratory diseases; On chip nested PCR; Microfluidic chip; Nasopharyngeal swab sample

资金

  1. German Federal Ministry for Education and Research (BMBF) [FKZ 16SV3318]

向作者/读者索取更多资源

Point-of-care (PoC) testing followed by personalized efficient therapy of infectious diseases may result in a considerable reduction of associated health care costs. Lab-on-a-chip (LoC) systems represent a potentially high efficient class of PoC tools. Here, we present a LoC system for automated pathogen analysis of respiratory viruses from nasopharyngeal specimens. The device prepares total nucleic acids from extracted swab samples using magnetic silica beads. After reverse transcription the co-purified viral RNA is amplified in accordance with the QIAplex multiplex PCR technology. Hybridized to corresponding QIAGEN LiquiChip beads and labelled with streptavidin R-phycoerythrin, the amplified target sequences are finally detected using a QIAGEN LiquiChip200 workstation. All chemicals needed are either stored freeze-dried on the disposable chip or are provided in liquid form in a reagent cartridge for up to 24 runs. Magnetic stir bars for mixing as well as turning valves with metering structures are integrated into the injection-moulded disposable chip. The core of the controlling instrument is a rotating heating bar construction providing fixed temperatures for fast cycling. PCR times of about half an hour (for 30 cycles) could be achieved for 120 mu l reactions, making this system the fastest currently available high-volume PCR chip. The functionality of the system was shown by comparing automatically processed nasopharyngeal samples to ones processed manually according to the QIAGEN ResPlex (TM) II Panel v2.0 respiratory virus detection kit. A prototype of the present instrument revealed slightly weaker signal intensities with a similar sensitivity in comparison to the commercially available kit and automated nucleic acid preparation devices, even without protocol optimization.

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