Labs-on-a-chip are useful to perform in situ clinical tests with instantaneous results.
In this work, the design phase of the development of a lab-on-a-chip is presented.
The device will be used to perform tests on physiological fluids. It will be able to test
8 components: calcium, chloride, creatinine, glucose, magnesium, total protein, urea
and uric acid. A sample of the physiological fluid reacts with several reagents and the
device measures the absorbance of the reaction products.
The lab-on-a-chip is composed of a microfluidic system and an optical detection
system. The first contains microchannels and micro-reactors fabricated using SU-8
techniques. The second includes CMOS photodetectors and readout electronics, as
well as optical filters fabricated using CMOS-compatible post-processing on top of
the photodetectors.
Careful design of the microfluidic system of a lab-on-a-chip requires knowledge of
the transport phenomena in the microchannels. Numerical methods are used to
simulate the electroosmotic flow, reaction and mixture in the system. Velocitypressure
formulation of the Navier-Stokes equations is solved by a finite difference
method. Mass transport equation is solved by a second order finite difference
method. For enzymatic reactions, biochemical reaction kinetics is considered.
Design choices are presented and explained. The final design of the microfluidic
system complies with layout restriction and kinetic, mass transport and other physical
limitations. The dimensions of the micro-reactors are optimized to maximize mixing.
The design of the optical detection system involves selection of the dielectric layers
available in the CMOS process for the photodetectors and selection of the dielectric
thin-films layers for the optical filters. An array of 8 selective optical filters is
designed for parallel testing of the 8 reported components. They are structurally
optimized for an optical response at the absorption peak of each reaction product.
The lab-on-a-chip output provides a digital signal for computer interfacing.R&D Centre Algoritmi.Escola de Engenharia da Universidade do Minho - Program IN2TEC.Fundação para a Ciência e a Tecnologia (FCT) - Grant SFRH/BPD/17689/2004