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  4. Capturing CD4 cells using a functionalized circular microfluidic device and glutaraldehyde as biolinker for tuberculosis detection and diagnosis
 
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Capturing CD4 cells using a functionalized circular microfluidic device and glutaraldehyde as biolinker for tuberculosis detection and diagnosis

Journal
Progress in Biomedical Optics and Imaging - Proceedings of SPIE
Journal Volume
9320
Date Issued
2015
Author(s)
Shih, Y.-F.
Huang, N.-T.
NIEN-TSU HUANG  
CHIH-KUNG LEE  
DOI
10.1117/12.2078693
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/486128
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84931863706&doi=10.1117%2f12.2078693&partnerID=40&md5=5797bc78a2622af3fca07164cb9b2404
Abstract
It is estimated that about one-third of the world?€?s population has already been infected by tuberculosis. Mycobacterium tuberculosis, in general, can result in an active case of tuberculosis in approximately 5%-10% of those who suffer from latent tuberculosis and the chance of becoming ill is the highest within one of year of getting the disease. Although a newly developed methods called interferon gamma release assay (IGRA) can monitor CD4 cells secreted cytokine to diagnose tuberculosis (TB) condition. However, it is difficult to count total numbers of cytokine secreted CD4 cells, which make the diagnosis less accurate. Therefore, we develop a functionalized polydimethylsiloxane (PDMS) device using glutaraldehyde to capture CD4 cells. To enhance the capture efficiency, we use COMSOL simulation to optimize the arrangement of PDMS micro pillars to make cells uniformly distributed in the device. Our preliminary data showed the microfluidic configuration in a circular shape with HCP patterned micro pillars turned 30 degrees offers the highest cell capture rate. ? 2015 SPIE.
SDGs

[SDGs]SDG3

Other Subjects
BioMEMS; Cells; Cytology; Diagnosis; Microchannels; Microsystems; Silicones; Tubes (components); Capture efficiency; Cell capture; Detection and diagnosis; Interferon-gamma; Micro-fluidic devices; Mycobacterium tuberculosis; Polydimethylsiloxane PDMS; tuberculosis; Microfluidics
Type
conference paper

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