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A7_Microfluidics_fundamentals_I

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Micropumps valveless

electrophoresis of a specific solute

E is field strength, q and r are the charge of the solute, η is the viscosity

electroosmosis of the bulk liquid

σ is the surface charge density of the channels and δ is the Debye double layer thickness, µ’s are the mobilities

surface charges

1

3.04

1010

 

 

Debye length depends on the molarity

M of the electrolyte in the buffer. As the ionic strength (or the number of charged ions increases, the Debye length decreases.

Pressure-driven vs. electroosmotic flow

Voltage-driven flow

Voltage applied at ends of a channel filled with electrically conductive liquid

parabolic (Poiseuille)

flat “plug-flow” profile

Electroosmotic flow speed, where ψs is the

 

 

surface (zeta) potential. Note that the flow

 

 

velocity does not depend on the size or

 

 

shape of the channel.

Multi-layer PDMS-based

LSI platform

The valve (left) can be closed by applying a pressure p to the control channel

Microfluidic realization of a free interface diffusion (FID) protein crystallization assay, based on the large scale integration platform (LSI). One unit cell consists of three crystallization cells for crystallization with different mixing ratios (a). They are initially filled with liquid while the central interface valve is closed (b). Afterwards, the interface valve is opened to allow diffusive mixing between the coupled chambers (c). The chip (d) consists of 48 cells for protein crystallization.

Capillary driven test strips

Centrifugal microfluidics

Principal centrifugal approach and schematic sketch of the three valving techniques on the centrifugal platform.

(A) geometric capillary valve, (B) hydrophobic valve and (C) hydrophilic siphon valve.

Microfluidic realization of a free interface diffusion (FID) protein crystallization assay, based on the centrifugal microfluidic platform.

Droplet based microfluidic platforms

Droplet based microfluidic platforms

Microfluidic realization of a protein crystallization assay, based on the pressure driven droplet-based platform. The protein and precipitation solution are continuously injected into one droplet of adjustable volume (a) and afterwards transported into a glass capillary for crystallization (b). Recirculating flows inside the droplets enhance mixing and induce the crystallization process (c).

Integrated lab-on-a-chip architecture for a colorimetric glucose assay, based on the droplet based electrowetting platform.

Four reservoirs with injection elements are connected to an electrode

circuit, where the droplets are mixed, split and transported to detection sites for readout

Class info

Microfluidics fundamentals II (A8)

HW4 – microfluidics– is available in the class homepage – due Sunday, October 13

Required reading: make sure you read and understand the microfluidics support papers

This week office hours: 10-12h on Thursday, October 10

Next week: no formal classes. Visit to INESC MN clean room – please sign-up

P1 papers expected to be available Sunday, October 13

A9 and A10 – case studies in biomicrofluidics; target capture in microchannels

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