Micro-fluidic chambers for use in a liquid medicament delivery system, include a bottom substrate and a top cover, the top cover being spaced from the bottom substrate so as to define a height of the chamber, wherein, one or more walls or fillings are positioned in the chamber, the walls or fillings defining a fluid channel there between such that the fluid channel extends from an inlet conduit to an inlet of the chamber to an outlet conduit connected to an outlet of the chamber, wherein, each of the walls or fillings has a height less than the height of the chamber so as to define a fluid gap between a top surface of each wall or filling and the top cover; and wherein, the dimensions of the walls or fillings and the chamber are such that the fluid gap will be filled with liquid by capillary forces via the fluid channel when liquid is introduced into the fluid chamber.

Various approaches of receiving signals in integrated circuitry include implementing two successive stages of signal manipulation and employing an interface having an AC coupling network and buffer circuits for decoupling the output impedance and common-mode level of the first stage of signal manipulation from the input impedance and common-mode level of the second stage of signal manipulation without degrading the performance of either stage.

A liquid-state nuclear-magnetic-resonance measurement cell includes a reservoir for a liquid medium; a fluidic circuit connected to the reservoir and comprising a measurement chamber; a gas injector opening into the fluidic circuit, at a distance from the measurement chamber; and a coil encircling the measurement chamber; wherein it also comprises at least one capacitive element forming, with the coil, an electromagnetic resonator; and in that it has a shape allowing its introduction into a nuclear-magnetic-resonance probe in replacement of an assembly formed by a nuclear-magnetic-resonance tube and a spinner bearing the tube, the coil encircling the measurement chamber being then positioned so as to couple by induction to at least one radiofrequency coil of the probe. Nuclear-magnetic-resonance measurement system comprising such a measurement cell. Magnetic-resonance measurement method using such a cell is also provided.

Various approaches of receiving signals in integrated circuitry include implementing a voltage-mode passive mixer for down-converting the frequency of the received signals, a baseband output buffer, and a transconductance amplifier coupled between the voltage-mode passive mixer and baseband output buffer for presenting a high-impedance load to the voltage-mode passive mixer and shielding the baseband output buffer from a high-frequency feedthrough.

A device for analyzing substances in a sample on the basis of a measurement of nuclear magnetic resonances including a magnetic field device configured to generate a magnetic field. The device is configured such that, in order to detect magnetic resonances induced in the sample by the generation of the magnetic field, provision is made of at least one magnetic field sensor which comprises at least one sensitive component with diamond structures. The diamond structures have nitrogen vacancy centers.

In a general aspect, a sample holder has multiple sample containers. In some instances, the sample holder can be received into a resonator package in a primary magnetic field of a magnetic resonance system. The resonator package includes a resonator configured to interact with a sample in a sample region. The sample holder includes a first sample and a calibration sample. The position of the sample holder relative to the resonator is calibrated. After calibrating the position of the sample holder, the sample holder is translated to position the first sample in the sample region. Magnetic resonance data is acquired based on magnetic resonance signals generated by an interaction between the resonator and the first sample.

Superparamagnetic nanoparticle-based analytical method comprising providing a sample having analytes in a sample matrix, providing a point of care chip having analytical regions, each of which is a stationary phase having at least one or more sections, labeling each of the analytes with a superparamagnetic nanoparticle and immobilizing the labeled analytes in the stationary phase, providing an analytical device having a means for exciting the superparamagnetic nanoparticles in vitro and a means for sensing, receiving, and transmitting response of the excited superparamagnetic nanoparticles, placing the chip in the analytical device and exciting the superparamagnetic nanoparticles in vitro, sensing, receiving, and transmitting the response of the superparamagnetic nanoparticles, and analyzing the response and determining characteristic of the analytes, wherein the response of the superparamagnetic nanoparticles comprises harmonics. The present invention also provides the hybrid point of care chip and analyzer to be used in the analytical method.

A palm-size portable NMR relaxometer system for performing multi-step multi-sample chemical/biological assays, comprising a PCB having a CMOS NMR transceiver and a DMF device integrated thereon. A portable magnet has an inner gap configured to at least partially receive the DMF device. The DMF device comprises a platform of electrodes including a sensing site and receives one or more samples for analysis at an electrode and automatically transports the one or more samples on individual paths sequentially to the sensing site, for performing sensing on each sample sequentially. A Butterfly coil disposed on the PCB and underneath the DMF device and is at least partially received in the inner gap. The Butterfly coil excites the sample at the NMR sensing site by transducing a magnetic field produced at the sensing site to an electrical signal which is processed by the CMOS NMR transceiver to produce an analytical signal.

In accordance with one aspect of this disclosure, there is provided a device for performing magnetic resonance relaxometry. The device comprises a radio-frequency spectrometer comprising at least one field-programmable gate array chip; a power amplifier electrically connected with the radio-frequency spectrometer and amplifying an electrical output of the radio-frequency spectrometer, thereby producing an amplified electrical signal comprising between about 0.1 Watts and about 10 Watts power; a duplexer configured to isolate the radio-frequency spectrometer from the amplified electrical signal during a receiving mode of the device; a radio-frequency detection probe configured to transmit radio-frequency electromagnetic radiation to excite nuclei under resonance during a transmission mode of the device, the radio-frequency detection probe comprising a detection coil comprising an inner diameter of less than about 1 millimeter; and at least one magnet supplying an external magnetic field to a detection region of the radio-frequency detection probe, the external magnetic field being less than about 3 Tesla.

A subterranean characterization and fluid sampling device includes a tool body, a probing module, and a permanent magnet. The tool body includes a fluid testing module configured to retain a fluid sample and an internal radio frequency coil disposed within the tool body and drivable to generate RF magnetic field B.sub.2. The probing module is coupled to the tool body and configured to withdraw the fluid sample from a formation and deliver the fluid sample to the fluid testing module. The probing module comprises an external antenna drivable to generate RF magnetic field B.sub.1. The permanent magnet induces static magnetic field B.sub.0. The permanent magnet is coupled to the tool body and external to the probing module.