A wireless power transfer system using an inductive link has been demonstrated for implantable sensor applications. The system is composed of two primary blocks: an inductive power transfer unit and a backward data communication unit. The inductive link performs two functions: coupling the required power from a wireless power supply system enabling battery-less, long-term implant operation and providing a backward data transmission path. The backward data communication unit transmits the data to an outside reader using FSK modulation scheme via the inductive link. To demonstrate the operation of the inductive link, a board-level design has been implemented with high link efficiency. Test results from a fabricated sensor system, composed of a hybrid implementation of custom-integrated circuits and board-level discrete components, are presented demonstrating power transmission of 125 mW with a 12.5% power link transmission efficiency. Simultaneous backward data communication involving a digital pulse rate of up to 10 kbps was also observed.
Wireless power transfer via inductive link is becoming a popular choice as an alternate powering scheme for biomedical sensor electronics. Spiral printed circuit board (PCB) inductors are gaining attractions for wireless power transfer applications due to their various advantages over conventional inductors such as low-cost, batch fabrication, durability, manufacturability on flexible substrates, etc. In this work, design of a multi-spiral stacked solenoidal inductor for biomedical application in 13.56 MHz band is presented. Proposed stacking method enhances the inductance density of the inductor for a given area. This paper reports an optimization technique for design and implementation of the PCB inductors. The proposed scheme shows higher inductance and better figure-of-merit values compared to PCB inductors reported in literature, which are desirable for wireless power transfer system.
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.
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