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Low voltage and low power are two key requirements for on-chip realization of wireless power and data telemetry for applications in biomedical sensor instrumentation. Batteryless operation and wireless telemetry facilitate robust, reliable, and longer lifetime of the implant unit. As an ongoing research work, this paper demonstrates a low-power low-voltage sensor readout circuit which could be easily powered up with an inductive link. This paper presents two versions of readout circuits that have been designed and fabricated in bulk complementary metal-oxide semiconductor (CMOS) processes. Either version can detect a sensor current in the range of 0.2 μA to 2 μA and generate square-wave data signal whose frequency is proportional to the sensor current. The first version of the circuit is fabricated in a 0.35-μ m CMOS process and it can generate an amplitude-shift-keying (ASK) signal while consuming 400 μ W of power with a 1.5-V power supply. Measurement results indicate that the ASK chip generates 76 Hz to 500 Hz frequency of a square-wave data signal for the specified sensor current range. The second version of the readout circuit is fabricated in a 0.5-μ m CMOS process and produces a frequency-shift-keying (FSK) signal while consuming 1.675 mW of power with a 2.5-V power supply. The generated data frequency from the FSK chip is 1 kHz and 9 kHz for the lowest and the highest sensor currents, respectively. Measurement results confirm the functionalities of both prototype schemes. The prototype circuit has potential applications in the monitoring of blood glucose level, lactate in the bloodstream, and pH or oxygen in a physiological system/environment.

The rich chemistry of polybenzoxazines allows a wide range of molecular structure design by using appropriate starting materials. A new class of polybenzoxazines has been developed from benzoxazine monomers containing pendent long aliphatic chains. The monomers have been synthesized by the reaction of phenol or bisphenol A with two different long-chain aliphatic amines. The chemical structure of the monomers was confirmed by 1 H nuclear magnetic resonance and Fourier transform infrared spectroscopy. The polymerization behavior of the monomers studied by differential scanning calorimetry shows exothermic peaks due to the ring-opening polymerization of benzoxazine monomers centered at 247-255 • C. Dynamic mechanical analysis indicated that the glass transition temperatures T g were in the range 81-92 • C. The thermal stability of the polymers was also examined by thermogravimetric analysis, demonstrating that the weight loss temperatures decreased in comparison with that of traditional polybenzoxazine.

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SUMMARY BackgroundTo decide when and how to treat children with chronic hepatitis C is an ongoing debate.

Monokine induced by interferon gamma (MIG/CXCL9) is used as an immune biomarker for early monitoring of transplant or allograft rejection. This paper demonstrates a direct electrical, label-free detection method of recombinant human MIG with anti-MIG IgG molecules in physiologically relevant buffer environment. The sensor platform used is a biologically modified GaN-based high electron mobility transistor (HEMT) device. Biomolecular recognition capability was provided by using high affinity anti-MIG monoclonal antibody to form molecular affinity interface receptors on short N-hydroxysuccinimide-ester functionalized disulphide (DSP) self-assembled monolayers (SAMs) on the gold sensing gate of the HEMT device. A floating gate configuration has been adopted to eliminate the influences of external gate voltage. Preliminary test results with the proposed chemically treated GaN HEMT biosensor show that MIG can be detected for a wide range of concentration varying from 5 ng/mL to 500 ng/mL.