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Online proceedings - EDA Publishing Association

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coupling rotation movement in the Y and X directions as shown<br />

in the X, Y, and Z components in Fig. 5. The area on the back of<br />

the cylinder also flows rotationally in the Z direction. Rotation<br />

in the Y direction was also generated at the end of the sensing<br />

field. The flow chart also reveals the chaotic flow effect that<br />

was generated in the microenvironment at this stage<br />

(a)<br />

(c)<br />

(d)<br />

Fig. 4 Vortices when (a) hc =300 m (b) hc = 400 m (c) hc = 500 m (d) hc =<br />

600 m<br />

(a)<br />

(b)<br />

(b)<br />

11-13 <br />

May, 2011, Aix-en-Provence, France<br />

<br />

PDMS solidifies after evacuation and heating. PDMS can be<br />

removed from the inserts. Additionally, the atmospheric<br />

pressure plasma can modify the convection channel and the<br />

PDMS surface of the substrate. The parameter 0.5 Torr, 29.6<br />

Watt, and 15 min~20 min represents pressure, plasma<br />

efficiency, and surface modification time. The microchannel<br />

was then connected with the substrate after PDMS was used to<br />

implement the surface modification procedure.<br />

3.2.2 Fluorescence streamline<br />

For this part of the study, we utilized fluorescent particles<br />

to examine the actual streamline condition of the microfluidics.<br />

The fluorescent particles used had a grain size of 10m,<br />

filtering band was between 460 and 490 nm. An Olympus IX71<br />

fluorescent microscope was used in a dark environment to<br />

provide the optical band that excites the particles, allowing the<br />

fluorescent particles to generate fluorescence automatically<br />

after photo-excitation in a specific band. When the fluorescent<br />

particles move with the streamline in the channel, the trajectory<br />

of the fluorescent particles reveals the actual streamline<br />

condition of the microfluidics. Fig. 6 (a) shows the<br />

experimental results of the fluorescent streamline. The fluid in<br />

the figure rotates in direction Y when entering the sensing field<br />

from the left. This is due to the height difference between the<br />

bottom face of the sensing field and the inlet. When the fluidics<br />

passes the cylindrical structure, it reveals an identical result to<br />

the estimation implemented by the finite element simulation<br />

software Fig. 6(b). The flow rate difference causes the fluid to<br />

rotate toward direction Z at the back of the cylindrical structure.<br />

(c)<br />

Fig. 5 Simulation result when flow rate is 0.614 μm/s(a)Vorticity, x component<br />

(b)Vorticity, y component(c)Vorticity, z component(d)Streamline<br />

3.2 Microenvironment design<br />

After analysis simulation by finite element software, a 1<br />

mm cylindrical structure was added to the microenvironment.<br />

The height of the structure was 500 m while the rate of flow in<br />

the inlet area was 1500 ml / hr . The simulation result showed that<br />

the vortices were generated when the structure had a large<br />

speed difference. This phenomenon creates more opportunities<br />

for viruses to collide with the sensing field, enhancing the<br />

efficiency of the virus attachment to the field. We also<br />

discovered that a relationship might exist between the strength<br />

distribution of curl at the back of the cylinder and the<br />

fluorescence strength distribution of the attachment experiment.<br />

We discuss this further in Section 5.<br />

3.3 Fluorescence streamline experiment<br />

3.3.1 Fabrication of microfluidics environment<br />

Firstly, stainless steel or brass was processed by a CNC<br />

milling machine to produce the inserts designed in the study.<br />

After the processed metal inserts were cleaned, PDMS and<br />

hardener were fully mixed in a ratio of 10:1, and then PDMS<br />

was poured into the channel and substrate inserts respectively.<br />

(d)<br />

(a)<br />

Fig. 6 Streamlines by(a)fluorescent particles (b)simulation<br />

IV. FABRICATION OF RECOGNITION LAYERS<br />

First, the substrate and the microfluidic channel were<br />

fabricated by PDMS casting. A layer of Au film was deposited<br />

on the substrate by sputtering. Then, 20 mM 11-MUA<br />

(11-mercaptoundecanoic acid) solution was injected on the<br />

sensor surface by the microfluidics system. This links the<br />

11-MUA with gold films as self-assembled monolayers. EDC<br />

and NHS solutions (molar ratio, 2:1) were then injected on the<br />

sensor surface by the microfluidics system. In the final step,<br />

TYMV particles with fluorescent particles (NCD4) in the<br />

buffer were introduced over the sensor surface at a different<br />

flow rate. In the meantime, the sensor surface was rinsed and<br />

dried in FPLC (Fast Protein Liquid Chromatography) to avoid<br />

nonspecific adhesion. A confocal microscope was then used to<br />

monitor the sensor surface.<br />

To avoid the low-quality MUA molecular layer from<br />

affecting the adhesion effect of TYMV, the study adopted<br />

NCD-4 fluorescent particles as the sample and carried out tests<br />

on the MUA molecular layers. By adopting a cross-linker<br />

mechanism, NCD-4 and MUA can respond and bond more<br />

(b)<br />

369

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