Electrochemical microelectrodes are commonly used to detect spikes of amperometric current that correspond to exocytosis of oxidizable transmitter from individual vesicles, i.e., quantal exocytosis. We are developing transparent multi- electrochemical electrode arrays on microchips in order to automate measurement of quantal exocytosis. Here we report development of an improved device to target individual cells to each microelectrode in an array. Efficient targeting (~75%) is achieved using cell-sized micro-well traps fabricated in SU-8 photoresist together with patterning of poly (L-lysine) in register with electrodes to promote cell adhesion. The surface between electrodes is made resistant to cell adhesion using poly (ethylene glycol) in order to facilitate movement of cells to electrode “docking sites”. We demonstrate the activity of the electrodes using the test analyte ferricyanide and perform recordings of quantal exocytosis from bovine adrenal chromaffin cells on the device. Multiple cell recordings on a single device demonstrate the consistency of spike measurements and multiple recordings from the same electrodes demonstrate that the device can be cleaned and reused without degradation of performance. The new device will enable high-throughput studies of quantal exocytosis and may also find application in rapidly screening drugs or toxins for effects on exocytosis.

Neurons and endocrine cells secrete neurotransmitter and hormones in discrete packets in a process called quantal exocytosis. Electrochemical microelectrodes can detect spikes in current resulting from the oxidation of individual quanta of transmitter only if the electrodes are small and directly adjacent to release sites on the cell. Here we report development of a microchip device that uses microfluidic traps to automatically target individual or small groups of cells to small electrochemical electrodes. Microfluidic channels and traps were fabricated by multi-step wet etch of a silicon wafer whereas Pt electrodes were patterned in register with the trap sites. We demonstrate high-resolution amperometric measurement of quantal exocytosis of catecholamines from chromaffin cells on the device. This reusable device is a step towards developing high-throughput lab-on-a-chip instruments for recording quantal exocytosis to increase the pace of basic neuroscience research and to enable screening of drugs that target exocytosis.

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This work reports on the synthesis and tunable characteristics of nanothermite compositions based on mesoporous Fe 2 O 3 as an oxidizer and Al nanoparticles as a fuel. The reactivity (rate of increase of pressure) and the combustion wave speed were determined to evaluate the performance of these composites for various applications. A gas generating polymer, (acrylamidomethyl) cellulose acetate butyrate (AAMCAB), was loaded in the mesopores of Fe 2 O 3 matrix following wet-impregnation technique. The samples prepared in this work were characterized by a number of analytical techniques such as Fourier transform infrared (FTIR) absorption spectroscopy, transmission and scanning electron microscopy (TEM, SEM), energy dispersive X-ray analysis, X-ray diffraction, and nitrogen adsorption -desorption isotherms. Then, mesoporous Fe 2 O 3 powder was mixed with Al nanoparticles to prepare nanoenergetic composites. The main characteristics such as peak pressure, reactivity, combustion wave speed, and pressure sustenance were determined as a function of polymer loading. The dependence of combustion wave speed on the pressure was established following the well-known Vieilles law. The small value of 0.408 for the pressure exponent indicates the suitability of these nanothermite compositions for propellant applications. By reducing the percentage of polymer, the characteristic properties of nanoenergetic composite can be suitably tuned for other applications.

We present a low cost, easy to fabricate biosensor, which can quickly and accurately detect Salmonella typhimurium. This study also compares the advantages of the microfluidic biosensor over a nonmicrofluidic biosensor. High density interdigitated electrode array was used to detect Salmonella cells inside a microfluidic chip. Monoclonal anti-Salmonella antibodies were allowed to be immobilized on the surface of the electrode array for selective detection of Salmonella typhimurium. An impedance analyzer was used to measure and record the response signal from the biosensor. The biosensor provides qualitative and quantitative results in 3 hours without any enrichment steps. The microfluidic biosensor's lower detection limit was found to be 3×10 3 CFU/mL compared to the 3×10 4 CFU/mL of the nonmicrofluidic biosensor, which shows that the microfluidic biosensor has 10-fold increased sensitivity. The impedance response of microfluidic biosensor was also significantly higher (2 to 2.9 times) compared to the nonmicrofluidic biosensor.