Lab-on-a-disk as a potential microfluidic platform for dengue NS1-ELISA

Detection of non-structural protein 1 (NS1) of dengue virus can gives early diagnosis of dengue and shows high sensitivity. Current technique uses for the dengue NS1 detection is enzyme-linked-immusorbent assay (ELISA) on 96 microwell plate. However, the assay requires long incubation time about 90...

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Bibliographic Details
Main Authors: Yusoff, N.A., Soin, N., Ibrahim, F.
Format: Conference or Workshop Item
Language:English
Published: 2009
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Online Access:http://eprints.um.edu.my/9301/1/Lab-on-a-disk_as_a_potential_microfluidic_platform_for_dengue_NS1-ELISA.pdf
http://eprints.um.edu.my/9301/
http://www.scopus.com/inward/record.url?eid=2-s2.0-76249118919&partnerID=40&md5=15c00c4b9c4e678c859ce6d62951b29a http://ieeexplore.ieee.org/xpls/absall.jsp?arnumber=5356330
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Summary:Detection of non-structural protein 1 (NS1) of dengue virus can gives early diagnosis of dengue and shows high sensitivity. Current technique uses for the dengue NS1 detection is enzyme-linked-immusorbent assay (ELISA) on 96 microwell plate. However, the assay requires long incubation time about 90 minutes (for antigen-antibody interaction) and total assay time takes almost 2 hours and 30 minutes to complete. Therefore, a lab-on-a-disk with applied centrifugal force is proposed as a potential microfluidic platform to reduce the assay time by effectively mix and separate liquid in the ELISA assay. The advantages of the technique are having large specific volume, short diffusion length, minimum reagents consumption and simplify procedures. The lab-on-a-disk will exploit centrifugal and capillary forces to act as a passive valve to control the flow sequence of different solutions involved. Each steps of the ELISA process is carried out automatically by controlling the rotation speed of the disk. This paper will describe the lab-on-a-disk platform on its microfluidic principles, fabrication process, detection systems, biosensor applications, and the proposed model for dengue NS1-ELISA assay. © 2009 IEEE.