This paper presents a functional on-chip pressure generator that utilizes chemical energy from a solid chemical propellant to perform fluidic delivery in applications of plastic-based disposable biochips or lab-on-a-chip systems. In this functional on-chip pressure generator, azobis-isobutyronitrile (AIBN) as the solid chemical propellant is deposited on a microheater using a screen-printing technique, which can heat the AIBN at 70 degrees C to produce nitrogen gas. The output pressure of nitrogen gas, generated from the solid chemical propellant, is adjustable to a desired pressure by controlling the input power of the heater. Using this chemical energy source, the generated pressure depends on the deposited amount of the solid chemical propellant and the temperature of the microheater. Experimental measurements show that this functional on-chip pressure generator can achieve around 3 000 Pa pressure when 189 mJ of energy is applied to heat the 100 microg of AIBN. This pressure can drive 50 nl of water through a microfluidic channel of 70 mm and cross-sectional area of 100 microm x 50 microm. Due to its compact size, ease of fabrication and integration, high reliability (no moving parts), biologically inert gas output along with functionality of gas generation, this pressure generator will be an excellent pressure source for handling the fluids of disposable lab-on-a-chip, biochemical analysis systems or drug delivery systems.

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Polyaniline (PANI) is one of the most studied and most stable electrically conductive polymers, with the conductive form being the navy blue emeraldine salt. However, PANI is very difficult to process and displays poor mechanical performance, which suggests improving its properties by developing composite systems. In the present approach, PANI was generated in situ in poly(dimethylsiloxane) (PDMS) networks. The color of the composites varied from brown, to blue, to greenish blue, with the blue samples being the most conductive. The chemical structures of the samples were studied using FT-IR/ATR spectroscopy, which confirmed that there was more conjugation in the more conductive samples.

Cyclic Olefin copolymers (COC) are a new class of polymers that may prove to be extremely useful in injection molding of micron scale fluidic devices. In microfluidic devices it is desirable to have a hydrophilic surface such as in flow driven by capillary action. However, such hydrophilic surfaces tend to display protein deposition when contacted with blood unlike hydrophobic surfaces. Alternatives to capillary action are then needed to control fluid flow for hydrophobic surfaces. Our goal in this research is to tune the slightly hydrophobic COC surfaces through simple surface modifications that are amenable to injection molding and other processing methods. In this study, the surface of an injection molded microfluidic component made from COC was modified in order to change the surface properties important to bio-fluidic devices. Some of the techniques used in this study were plasma treatments and ASG (aerosol gel) coating. Plasma treatments were conducted by using O2, CF4 and their combination gas. O2 treated surfaces became hydrophilic with increasing time of treatment. Combining O2 and CF4 made the surfaces more hydrophobic compared to CF4 only. The structural changes after the plasma treatments were examined by ATR (Attenuated Total Reflectance) spectroscopy. Titania and silica particles from the ASG process were synthesized from titanium iso-propoxide and tetraethoxysilane, respectively. Titania coated surfaces became more hydrophilic and the silica coated surfaces did not have much change in their surface characteristics. The hydrophobicity of the plastic surfaces was measured by their contact angle with water. The implication of these treatments on bio-fluidic devices and their adaptation to the injection molding process will also be discussed.

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